Search tips
Search criteria 


Logo of mbcLink to Publisher's site
Mol Biol Cell. 2010 August 15; 21(16): 2930–2943.
PMCID: PMC2921114
A Highlights from MBoC Selection

EHBP-1 Functions with RAB-10 during Endocytic Recycling in Caenorhabditis elegans

Francis A. Barr, Monitoring Editor


Caenorhabditis elegans RAB-10 functions in endocytic recycling in polarized cells, regulating basolateral cargo transport in the intestinal epithelia and postsynaptic cargo transport in interneurons. A similar role was found for mammalian Rab10 in MDCK cells, suggesting that a conserved mechanism regulates these related pathways in metazoans. In a yeast two-hybrid screen for binding partners of RAB-10 we identified EHBP-1, a calponin homology domain (CH) protein, whose mammalian homolog Ehbp1 was previously shown to function during endocytic transport of GLUT4 in adipocytes. In vivo we find that EHBP-1-GFP colocalizes with RFP-RAB-10 on endosomal structures of the intestine and interneurons and that ehbp-1 loss-of-function mutants share with rab-10 mutants specific endosome morphology and cargo localization defects. We also show that loss of EHBP-1 disrupts transport of membrane proteins to the plasma membrane of the nonpolarized germline cells, a defect that can be phenocopied by codepletion of RAB-10 and its closest paralog RAB-8. These results indicate that RAB-10 and EHBP-1 function together in many cell types and suggests that there are differences in the level of redundancy among Rab family members in polarized versus nonpolarized cells.


The endocytic pathways of eukaryotes regulate the uptake, sorting, and the subsequent recycling or degradation of macromolecules, fluid, membranes, and membrane proteins. After endocytosis through either clathrin-dependent or one of several clathrin-independent uptake mechanisms (Nichols, 2003 blue right-pointing triangle; Gesbert et al., 2004 blue right-pointing triangle), cargo proteins are delivered to early endosomes, where sorting occurs. Some cargo will be sorted for delivery to lysosomes for degradation (Mukherjee et al., 1997 blue right-pointing triangle), whereas others will be directly or indirectly routed back to the plasma membrane or Golgi apparatus through various recycling pathways (Maxfield and McGraw, 2004 blue right-pointing triangle; Rojas et al., 2007 blue right-pointing triangle; Grant and Donaldson, 2009 blue right-pointing triangle).

The Rab family of GTPases function as master regulators, controlling diverse aspects of intracellular trafficking and organelle identity (Stenmark, 2009 blue right-pointing triangle). Like other Ras superfamily GTPases, Rabs cycle between an active GTP-bound state and an inactive GDP-bound state. Through their direct or indirect interactions with effectors and binding proteins, Rabs function as coordinators of intracellular trafficking events, often controlling motor-based delivery of vesicles and vesicle tethering, and in some cases affecting cargo recruitment, vesicle budding, and vesicle fusion with target compartment membranes (Grosshans et al., 2006 blue right-pointing triangle; Stenmark, 2009 blue right-pointing triangle).

Rabs have been shown to regulate both fast recycling directly from early endosomes and slow recycling from the endocytic recycling compartment (ERC; Grant and Donaldson, 2009 blue right-pointing triangle). Rab4 was identified as an important regulator of transferrin receptor (TfR) recycling (van der Sluijs et al., 1992 blue right-pointing triangle), although the precise function of Rab4 in recycling remains unclear. Studies by Kouranti et al. (2006) blue right-pointing triangle indicated that Rab35 is also an important regulator of TfR rapid recycling, whereas other studies indicate a role for Rab35 on the Arf6- and EHD1-containing tubular endosomes of the slow recycling pathway (Walseng et al., 2008 blue right-pointing triangle; Allaire et al., 2010 blue right-pointing triangle). Another well-established Rab involved in recycling is Rab11, a resident of the ERC that mediates recycling from the ERC to the plasma membrane (Powelka et al., 2004 blue right-pointing triangle; Weigert et al., 2004 blue right-pointing triangle). In polarized cells, Rab11 activity appears restricted to the apical membrane, whereas other proteins must regulate recycling to the basolateral surface. Thus, polarized cells appear to use different mechanisms to regulate trafficking at their distinct, specialized membrane surfaces.

Regulated recycling has also been demonstrated in nonpolarized cells. Interestingly, such cells still employ multiple mechanisms in the trafficking of different recycling cargo. For instance in HeLa cells Arf6 and Rab22a are important for the recycling of major histocompatibility complex (MHC) class I and TAC (IL2-receptor α chain), but have little or no effect on TfR (Weigert et al., 2004 blue right-pointing triangle). MHCI and TAC are internalized by clathrin-independent endocytosis (CIE), whereas TfR is internalized by clathrin-dependent endocytosis (CDE). The two cargo classes appear to converge in the endosomal system after uptake, but diverge again upon exit from the ERC. It remains unclear if their divergence in recycling is related to the difference in their uptake routes. Rab11 and EHD1 proteins are important for the recycling of both cargo types, although there are likely to be differences in the mechanisms used to recycle these two cargo types.

RAB-10 has been implicated in the recycling of clathrin-independent cargo in the Caenorhabditis elegans intestine, probably at the level of transport between early endosomes and recycling endosomes (Chen et al., 2006 blue right-pointing triangle). Recent work in C. elegans suggests that interneuron postsynaptic glutamate receptor recycling also requires RAB-10 (Glodowski et al., 2007 blue right-pointing triangle). In mammalian systems, Rab10 has been implicated in basolateral recycling in Madin-Darby canine kidney (MDCK) cells and in Glut4 recycling in adipocytes (Babbey et al., 2006 blue right-pointing triangle; Sano et al., 2007 blue right-pointing triangle). RAB-10, and another similar GTPase, RAB-8, are the closest metazoan relatives of yeast Sec4p, the final Rab in the yeast secretory pathway. Rab8 has been suggested to function in the secretory pathway in mammalian cells (Hattula et al., 2002 blue right-pointing triangle; Ang et al., 2003 blue right-pointing triangle), and this delivery process may use the recycling endosomes as an intermediate (Ang et al., 2004 blue right-pointing triangle; Henry and Sheff, 2008 blue right-pointing triangle). In polarized MDCK cells, simultaneous knockdown of Rab8 and Rab10 produced more severe exocytosis defects than individual knockdown (Schuck et al., 2007 blue right-pointing triangle), implying that Rab8 and Rab10 may function redundantly in exocytic membrane trafficking, perhaps by sharing some effectors. Whether the different Rabs that regulate distinct recycling pathways use different effector molecules remains an open question.

Here we report the physical association of RAB-10 and -8 with the effector molecule EHBP-1. We show that ehbp-1 mutants share several specific recycling defects with rab-10 mutants, including preferential effects on the CIE cargo protein TAC in the intestine. We also provide evidence that EHBP-1 functions with RAB-10 in neurons and regulates germ cell growth in a pathway that is redundantly regulated by RAB-10 and -8. Surprisingly, unlike conventional Rab effectors, our results suggest that EHBP-1 functions upstream of RAB-10 and is important for the endosomal association of RAB-10.


General Methods and Strains

All C. elegans strains were derived originally from the wild-type Bristol strain N2. Worm cultures, genetic crosses, and other C. elegans husbandry were performed according to standard protocols (Brenner, 1974 blue right-pointing triangle). Strains expressing transgenes were grown at 20°C. A complete list of strains used in this study can be found in Supplementary Table 1.

RNA interference (RNAi) was performed using the feeding method (Timmons and Fire, 1998 blue right-pointing triangle). Feeding constructs were either from the Ahringer library (Kamath and Ahringer, 2003 blue right-pointing triangle) or were prepared by PCR from EST clones provided by Dr. Yuji Kohara (National Institute of Genetics, Japan) followed by subcloning into the RNAi vector L4440 (Timmons and Fire, 1998 blue right-pointing triangle). For most experiments synchronized L1 or L4 stage animals were treated for 24–72 h and were scored as adults.


The following antibodies were used in this study: mouse anti-HA mAb (16B12; Covance Research Products, Berkeley, CA), rabbit anti-GST polyclonal antibody (Z-5; Santa Cruz Biotechnology. Santa Cruz, CA).

Yeast Two-Hybrid Analyses

Yeast two-hybrid screen for candidates of RAB-10–interacting proteins was performed according to the procedure of the DupLEX-A yeast two-hybrid system (OriGene Technologies, Rockville, MD). The cDNA sequences of C. elegans rab-10(Q68L) in the entry vector pDONR221 were cloned into the pEG202-Gtwy bait vector by Gateway recombination cloning (Invitrogen, Carlsbad, CA) to generate N-terminal fusions with the LexA DNA-binding domain. The pEG202-rab-5(Q78L), rab-7(Q68L), rab-8(Q67L), rab-11(Q70L), rab-35(Q69L), rme-1 and inactive rab-10(QT23N), and rab-8(QT23N) were constructed accordingly. The prenylation motifs for membrane attachment at the C-terminal ends of each RAB were also deleted to improve entry of bait fusion proteins into the yeast nucleus. The C. elegans cDNA library was purchased from the DupLEX-A yeast two-hybrid system (OriGene Technologies, Rockville, MD).

All two-hybrid plasmids were generated as PCR products with Gateway attB.1 and attB.2 sequence extensions and were introduced into the Gateway entry vector pDONR221 by BP reaction. The bait vector pEG202-Gtwy and target vector pJG4–5-Gtwy have been described previously (Sato et al., 2008b blue right-pointing triangle). Prey plasmids encoded EHBP-1 truncations were amplified from C. elegans EST clone yk1543d03 (Dr. Yuji Kohara), and all amplified regions were confirmed by DNA sequencing. OriGene plasmid pSH18–34 [URA3, 8 ops.-LacZ] was used as reporter in all the yeast two-hybrid experiments. Constructs were introduced into the yeast strain EGY48 [MATα trp1 his3 ura3 leu2::6 LexAop-LEU2] included in the system. Transformants were selected on plates lacking leucine, histidine, tryptophan, and uracil, containing 2% galactose/1% raffinose at 30°C for 3 d and assayed for the expression of the LEU2 reporter. Blue/white β-galactosidase assays confirmed results shown for growth assays, according to manufacturer's instructions.

Tissue-specific Steady-State Endocytosis Assays

Intestinal basolateral endocytosis was visualized using muscle-secreted green fluorescent protein (GFP; transgenic strain arIs37[myo-3::ssGFP]) as a fluid-phase marker in a cup-4 mutant background. The cup-4 mutation was included to reduce uptake by coelomocytes and increase availability of the marker in the body cavity (Patton et al., 2005 blue right-pointing triangle).

Protein Expression and Coprecipitation Assays

N-terminally hemagglutinin (HA)-tagged proteins, RAB-5(Q78L), RAB-7(Q68L), RAB-8(Q67L), and RAB-10(Q68L), were synthesized in vitro using the TNT-coupled transcription-translation system (Promega, Madison, WI) using DNA templates pcDNA3.1–2xHA-RAB-5(Q78L), pcDNA3.1–2xHA-RAB-7(Q68L), pcDNA3.1–2xHA-RAB-8(Q67L), and pcDNA3.1–2xHA-RAB-10(Q68L), respectively (1.6 μg/each 50-μl reaction). The reaction cocktail was incubated at 30°C for 90 min. Control glutathione S-transferase (GST) and GST-EHBP-1(aa 662–901) fusion proteins were expressed in the ArcticExpress strain of Escherichia coli (Stratagene, La Jolla, CA). Bacterial pellets were lysed in 10 ml B-PER Bacterial Protein Extraction Reagent (Pierce, Rockford, ILL) with Complete Protease Inhibitor Cocktail Tablets (Roche, Indianapolis, IN). Extracts were cleared by centrifugation, and supernatants were incubated with glutathione-Sepharose 4B beads (Amersham Pharmacia, Piscataway, NJ) at 4°C overnight. Beads were then washed six times with cold STET buffer (10 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1 mM EDTA, 0.1% Tween-20). In vitro–synthesized HA-tagged protein (10 μl TNT mix diluted in 500 μl STET) was added to the beads and allowed to bind at 4°C for 2 h. After six additional washes in STET the proteins were eluted by boiling in 30 μl 2× SDS-PAGE sample buffer. Eluted proteins were separated on SDS-PAGE (10% polyacrylamide), blotted to nitrocellulose, and probed with anti-HA (16B12). Subsequently the blots were stripped and reprobed with anti-GST (Z-5) antibodies.

Plasmids and Transgenic Strains

rab-5(Q78L), rab-7(Q68L), rab-8(Q67L), and rab-10(Q68L) cDNA clones were transferred into an in-house modified vector pcDNA3.1 (+) (Invitrogen) with 2xHA epitope tag and Gateway cassette (Invitrogen) for in vitro transcription/translation experiments. For GST pulldown experiments an equivalent ehbp-1(aa 662–901) PCR product was introduced in frame into vector pGEX-2T (GE Healthcare Life Sciences, Piscataway, NJ) modified with a Gateway cassette.

To construct the GFP-tagged ehbp-1 transgene driven by its own promoter, ehbp-1 genomic sequences and presumed promoter sequences were PCR amplified from C. elegans genomic DNA, cloned into the entry vector pDONR221, and then transferred into the C. elegans pPD117.01 vector with Gateway cassettes (Invitrogen) followed by GFP coding sequences, let-858 3′ UTR sequences and the unc-119 gene of C. briggsae. The GFP-tagged plasmids (10 μg each) were bombarded into unc-119(ed3) mutant animals to establish low copy integrated transgenic lines by microparticle bombardment method (Praitis et al., 2001 blue right-pointing triangle). Integrated transgenic lines used in this study are listed in Supplementary Table 1.

To construct GFP or RFP/mCherry (a gift from R. Tsien, University of California, San Diego) fusion transgenes for expression specifically in the worm intestine, a previously described vha-6 promoter-driven vector modified with a Gateway cassette inserted at the Asp718I site just upstream of the GFP or red fluorescent protein (RFP) coding region was used. The sequences of C. elegans ehbp-1(cDNA) and ehbp-1(aa1–711) lacking a stop codon were cloned individually into entry vector pDONR221 by PCR and BP reaction, and then transferred into intestinal expression vectors by Gateway recombination cloning LR reaction to generate C-terminal fusions (Chen et al., 2006 blue right-pointing triangle). Complete plasmid sequences are available on request. Low copy integrated transgenic lines for all of these plasmids were obtained by the microparticle bombardment method (Praitis et al., 2001 blue right-pointing triangle).

Transgenic strains used in the GLR-1 glutamate receptor trafficking study were isolated after microinjecting various plasmids (5–50 ng/μl) along with rol-6dm (a gift from C. Mello, University of Massachusetts Medical School) or ttx-3::rfp as a transgenic marker (monomeric RFP; a gift from R. Tsien). Plasmids containing the glr-1 promoter, followed by a gene encoding either RFP::RAB-10 or EHBP-1::GFP, were introduced into the germline by microinjection or microparticle bombardment, and followed as extrachromosomal arrays. To generate these plasmids, LR reactions (Gateway Technology; Invitrogen) were performed using entry clones containing genomic DNA encoding EHBP-1 or cDNA encoding RAB-10. For these reactions, the destination vector, which contains the glr-1 promoter upstream of a ccdB gene that is flanked by attR sites, was generated from the plasmid pV6 (a gift from V. Maricq, University of Utah), following manufacturer's protocols (Invitrogen). For RFP-RAB-10, stable transgenic lines, including odIs42, were obtained by γ-irradiation followed by four generations of backcrossing.

Microscopy and Image Analysis

Live worms were mounted on 2% agarose pads with 10 mM levamisol as described previously (Sato et al., 2005 blue right-pointing triangle). Multiwavelength fluorescence images were obtained using an Axiovert 200M (Carl Zeiss MicroImaging, Oberkochen, Germany) microscope equipped with a digital CCD camera (C4742–12ER, Hamamatsu Photonics, Hamamatsu, Japan), captured using Metamorph software ver. 6.3r2 (Universal Imaging, West Chester, PA) and then deconvolved using AutoDeblur Gold software ver. 9.3 (AutoQuant Imaging, Watervliet, NY). Images taken in the DAPI channel were used to identify broad-spectrum intestinal autofluorescence caused by lipofuscin-positive lysosome-like organelles (Clokey and Jacobson, 1986 blue right-pointing triangle; Hermann et al., 2005 blue right-pointing triangle). To obtain images of GFP fluorescence without interference from autofluorescence, we used argon 488-nm excitation and the spectral fingerprinting function of the Zeiss LSM510 Meta confocal microscope system (Carl Zeiss MicroImaging) as described previously (Chen et al., 2006 blue right-pointing triangle). Quantification of images was performed with Metamorph software ver. 6.3r2 (Universal Imaging). Most GFP/RFP colocalization experiments were performed on L3 and L4 larvae expressing GFP and RFP markers as previously described.

For fluorescence microscopy of C. elegans ventral cord neurites, details were as described previously, but with some modifications (Glodowski et al., 2007 blue right-pointing triangle). GFP- and RFP-tagged fluorescent proteins were visualized in nematodes by mounting young adults (16–18 h post-L4 stage) on 2% agarose pads with 100 mM tetramisole in M9 buffer. Fluorescent images were obtained using an Axioplan II (Carl Zeiss, Thornwood, NY). A 100× (NA 1.4) PlanApo objective was used to detect GFP and RFP signals. Imaging was done with an ORCA charge-coupled device camera (Hamamatsu, Bridgewater, NJ) by using iVision software (Scanalytics, Fairfax, VA). Exposure times were chosen to fill the 12-bit dynamic range without saturation. Maximum intensity projections of z-series stacks were obtained, and out-of-focus light was removed with a constrained iterative deconvolution algorithm. Puncta outlines were automatically calculated for fluorescent signals that were two SDs above the unlocalized baseline by using a macro written for ImageJ64 software ( Puncta size was measured as the maximum diameter for each outlined cluster. Puncta outline data included both small puncta (e.g., as observed GLR-1-GFP and GFP-RAB-10 in wild type, classified based on a diameter cutoff of <1 μm and circular morphology using a program written in ImageJ), as well as long accretions (e.g., as observed GFP-RAB-10 in wild-type and GLR-1-GFP in rab-10 and ehbp-1 mutants, classified based on a width cutoff of >1 μm and elongated morphology). Numbers were calculated by counting the average number of small puncta or large accretions per 10 or 100 μm of neurite length, respectively.

Behavioral Assays

The reversal frequency of individual animals was assayed as described previously, but with some modifications (Zheng et al., 1999 blue right-pointing triangle). Single young adult hermaphrodites were placed on nematode growth medium plates in the absence of food. The animals were allowed to adjust to the plates for 5 min, and the number of spontaneous reversals for each animal was counted over a 5-min period. Thirty animals were tested for each genotype, and the reported scores reflect the mean number of reversals per minute.

Protein Secretion Assay in the C. elegans Germline

The generation of a C. elegans strain expressing mCherry-PH PLC1δ1 has been described previously (Kachur et al., 2008 blue right-pointing triangle). A GFP fusion to SNB-1 (T10H9.4) was generated by cloning the unspliced genomic locus into the SpeI site of pIC26 (GFP; Cheeseman et al., 2004 blue right-pointing triangle). The construct was integrated into DP38 [unc-119 (ed3)] as described previously (Praitis et al., 2001 blue right-pointing triangle) using a particle delivery system (Biolistic PDS-1000/He; Bio-Rad Laboratories, Richmond, CA).

Double-stranded RNA (dsRNA) was prepared as described previously (Oegema et al., 2001 blue right-pointing triangle) from templates prepared by using the primers listed (below) to amplify N2 genomic DNA. For depletions, L4 hermaphrodites were injected with dsRNA and incubated at 20°C for 45 h before analysis. The following primers were used: RNA 210, D1037.4, RAB-8, 1.9 mg/ml: oligo 1: AATTAACCCTCACTAAAGGgcttttgcatgccaagatgtc and oligo 2: TAATACGACTCACTATAGGCGGGACGAAAATGGTAAAAA; RNA 311, T23H2.5, RAB-10, 2.3 mg/ml: oligo 1: AATTAACCCTCACTAAAGGGTGCTGCTAATAGGCGACTCA and oligo 2: TAATACGACTCACTATAGGTTGCTCGTCAGTGGAATCAG; and RNA KOEHBP-1, F25B3.1, EHBP-1, 2.4 mg/ml: oligo 1: AATTAACCCTCACTAAAGGGATTTCAGTTCGTCCCCAATG and oligo 2: TAATACGACTCACTATAGGACGAATTGCTCCAACTCCTG.

For analysis of gonads, animals were anesthetized in 0.1% tricane (Sigma, St. Louis, MO), mounted on agarose pads and imaged at 20°C on a spinning disk confocal (Eclipse TE2000-E; Nikon, Melville, NY) microscope equipped with a Nikon 60×, 1.4NA PlanApo oil objective lens and a Hamamatsu ORCA-ER CCD camera. Line-scan analysis was performed using Metamorph software (Universal Imaging).


EHBP-1 Associates with Active GTP-bound RAB-10

To identify other proteins that function with RAB-10 in endocytic recycling, we performed a yeast two-hybrid screen for binding partners of the active GTP-bound form of RAB-10, using a predicted constitutively active mutant, RAB-10(Q68L), as bait. We identified 27 positive interacting clones encoding C-terminal portions of EHBP-1, the only C. elegans homolog of mammalian Ehbp1, a protein previously implicated in Glut4 trafficking in mammalian adipocytes (Guilherme et al., 2004b blue right-pointing triangle). Previous reports on mammalian Ehbp1 had not linked it to a Rab GTPase, but rather to EHD1 and EHD2, two membrane-associated proteins of the RME-1 ATPase family, which function in membrane tubulation and potentially in membrane fission (Guilherme et al., 2004b blue right-pointing triangle; Pant et al., 2009 blue right-pointing triangle). The smallest recovered interacting clone encompassed EHBP-1 amino acids 662–901 (Figure 1A and Materials and Methods). We further delimited the RAB-10–interacting domain of EHBP-1 to amino acids 712–851, a predicted coiled-coil region of the protein (Figure 1, C and D). No interaction could be detected between the C-terminal region of EHBP-1 and RAB-10(T23N), a predicted constitutively inactive GDP-bound mutant form of the Rab (Figure 1B and Supplemental Figure S1, A and B). These data suggest that EHBP-1 specifically binds to the active GTP-bound form of RAB-10.

Figure 1.
EHBP-1 physically interacts with RAB-10(Q68L) and RAB-8(Q67L). (A) Glutathione beads loaded with recombinant GST or GST-EHBP-1(aa 662–901) were incubated with in vitro–expressed HA-tagged RAB-5(Q78L), RAB-7(Q68L), RAB-8(Q67L), and RAB-10(Q68L) ...

We next screened other Rab GTPases for their ability to bind EHBP-1 using the yeast two-hybrid system. We found that GTP-bound RAB-8(Q67L), but not GDP-bound RAB-8(T23N), also bound to EHBP-1, including the minimal binding domain of EHBP-1(aa 712–851) defined by interaction with RAB-10 (Figure 1B and Supplemental Figure S2). RAB-8 is the closest paralog of RAB-10 in C. elegans, and together RAB-8 and -10 represent a branch of the metazoan Rabs that in vertebrates also includes Rab13, which is not present in the worm (Pereira-Leal and Seabra, 2001 blue right-pointing triangle). We did not detect interactions between EHBP-1 and the active forms of several other Rabs, including RAB-5, -7, -11, or -35 (Figure 1B). We further confirmed the binding interaction between RAB-8/10 with EHBP-1 using an in vitro GST-pulldown assay (Figure 1A and Materials and Methods). Surprisingly, this assay also detected a weak interaction with RAB-5(Q78L) that could not be detected using the two-hybrid method (Figure 1A). Together, these data indicate that EHBP-1 is a Rab-interacting protein, with a strong preference for the active forms of RAB-8 and -10.

In previous studies, we showed that RME-1, a regulator of endocytic recycling, functions downstream of RAB-10 (Chen et al., 2006 blue right-pointing triangle). Two mammalian homologues of RME-1, called EHD1 and EHD2, have been shown to interact with Ehbp1 in a manner dependent on the five closely spaced NPF motifs within Ehbp1 (Guilherme et al., 2004a blue right-pointing triangle,b blue right-pointing triangle). However, C. elegans EHBP-1 lacks NPF motifs, and we were unable to detect any interaction between the C. elegans proteins RME-1 and EHBP-1 using the yeast two-hybrid system, suggesting that this interaction is not conserved (Figure 1B and Supplemental Figure S1, C and D). Indeed, sequence alignment of Ehbp1/EHBP-1 orthologues shows that the NPF motifs are well conserved among vertebrate Ehbp1 homologues, but are absent in invertebrate Ehbp1 homologues (Supplemental Figure S3A, highlighted in pink). The acquisition of EHD-binding capacity through NPF-motifs may represent a vertebrate innovation in an otherwise ancient protein family.

EHBP-1 Is Widely Expressed in C. elegans

RAB-10 has been shown to be ubiquitously expressed in C. elegans (Chen et al., 2006 blue right-pointing triangle). To determine the expression pattern and subcellular localization of EHBP-1, we established transgenic lines expressing an EHBP-1-GFP fusion protein, driven by ehbp-1 upstream sequences (the predicted promoter region). EHBP-1-GFP fusion proteins were expressed in all somatic C. elegans tissues, including the pharynx and nerve ring, body-wall muscles, seam cells, intestine, oviduct sheath cell, and spermatheca (Figure 2, A–F). Thus EHBP-1 has the potential to interact with RAB-10 in all tissues. The EHBP-1-GFP fusion protein was localized in a punctate or tubular pattern in most tissues. In the intestine, EHBP-1-GFP was localized to both the apical and basolateral plasma membranes (Figure 2E). Near basolateral membranes, EHBP-1-GFP labels distinct cytoplasmic puncta resembling endosomes ranging in size from 0.5 to 1.0 μm (Figure 2D). In addition to punctate structures, EHBP-1-GFP also labeled tubular structures close to the basolateral plasma membrane of the intestine (Figure 2D).

Figure 2.
EHBP-1 is broadly expressed in C. elegans. Confocal images of EHBP-1-GFP transgene expression driven by the ehbp-1 promoter. Tissue-specific expression was observed as follows: (A) pharynx (arrows), nerve ring (arrowhead); (B) myofilament of body-wall ...

EHBP-1 Is Associated with Endosomes But Not Golgi in the Intestine

To determine where EHBP-1 is normally localized and to help test the hypothesis that EHBP-1 functions with RAB-10 in endocytic recycling, we performed a series of colocalization studies in the intestinal cells of living animals, comparing functional GFP-tagged EHBP-1 with a set of RFP-tagged endosomal markers described previously (Chen et al., 2006 blue right-pointing triangle). We observed the highest degree of colocalization of EHBP-1-GFP with RFP-RAB-10– and RFP-RAB-8–labeled endosomal puncta in the intestine (Figure 3, B–C). In polarized MDCK cells, Rab10 labels the common recycling endosome, and our previous work in C. elegans had indicated a function for RAB-10 in transport between basolateral early and recycling endosomes (Babbey et al., 2006 blue right-pointing triangle; Chen et al., 2006 blue right-pointing triangle). Rab8 has also been reported to regulate endocytic recycling in mammals, affecting the recycling of clathrin-independent cargos such as MHCI as well as clathrin-dependent cargo Tf (Hattula et al., 2006 blue right-pointing triangle). In the C. elegans intestine, we find that RFP-RAB-10 and GFP-RAB-8 colocalize extensively (Supplemental Figure S4, A–B). Closer examination showed that EHBP-1 colocalized with RAB-10 and -8 on punctate endosomal membranes. EHBP-1 also localized to tubular elements associated with the puncta and the plasma membrane (see Figure 6D). These results are consistent with EHBP-1 functioning with RAB-10 and/or -8 in vivo.

Figure 3.
EHBP-1 colocalizes with RAB-10 and -8 on endosomes. All images are from deconvolved 3D image stacks acquired in intact living animals expressing GFP- and RFP-tagged proteins specifically in intestinal epithelial cells. (A–A″) Arrowheads, ...
Figure 6.
RAB-10–positive endosomal labeling dramatically decreases in ehbp-1(tm2523) mutants, but accumulate significantly in rme-1(b1045) mutants (A–C and H). Representative confocal images of wild-type animals and mutants are shown for GFP-RAB-10 ...

EHBP-1 occasionally colocalized with basolateral recycling endosome marker RME-1 (Figure 3, D–D″), as we had found previously for RAB-10 (Chen et al., 2006 blue right-pointing triangle). EHBP-1-GFP also occasionally overlapped with the early endosome marker RFP-RAB-5, but the EHBP-1-GFP–labeled structures more often localized near RFP-RAB-5 puncta rather than overlapping with them directly (Figure 3, A–A″). EHBP-1-GFP was not found to colocalize with the apical recycling marker RFP-RAB-11 or the Golgi marker MANS-RFP (Figure 3, E–F″). Taken together these results indicate that EHBP-1 is enriched on endosomes, where it could potentially interact with RAB-10 and -8 to regulate endosome-to-plasma membrane transport of cargo.

Loss of EHBP-1 Causes Endocytic Recycling Defects

Loss of RAB-10 results in dramatic endocytic trafficking defects in the C. elegans intestine (Chen et al., 2006 blue right-pointing triangle). One of the most obvious phenotypes observed in RAB-10 loss-of-function animals is the formation of grossly enlarged intestinal endosomes that are filled with fluid-phase markers taken up from the basolateral surface (Fares and Greenwald, 2001 blue right-pointing triangle; Chen et al., 2006 blue right-pointing triangle). To determine if EHBP-1 shares some functions with RAB-10 in vivo, we first analyzed the intestines of animals depleted of EHBP-1 by RNAi-mediated knockdown or of animals containing a deletion allele of ehbp-1 obtained from the National Bioresource Project for the Experimental Animal “Nematode C. elegans” in Japan. This ehbp-1 mutant allele, tm2523, deletes 503 base pairs of genomic DNA corresponding to portions of the fifth and sixth exons and is predicted to place all coding regions downstream of the deletion out of frame, effectively truncating any remaining expressed protein after amino acid 302.

ehbp-1(RNAi) animals were slow growing and produced fewer progeny than control animals, whereas ehbp-1(tm2523) animals often arrested as larvae, and animals that reached adulthood were sterile (see below). ehbp-1(RNAi)-treated animals contained grossly enlarged intestinal endosomes that could be filled with a signal sequence–modified form of GFP (ssGFP) that is secreted from body-wall muscle cells (Fares and Greenwald, 2001 blue right-pointing triangle), a phenotype very similar to that produced by rab-10 loss-of-function mutants or rab-10(RNAi) (Figure 4, B and D; Chen et al., 2006 blue right-pointing triangle). Such vacuolated structures were also visible in the intestine of homozygous ehbp-1(tm2523) mutant animals and could be rescued by intestine specific expression of EHBP-1-GFP (Supplemental Figure S4, C–D′). ehbp-1 RNAi knockdown was considered effective because it blocked expression of EHBP-1-GFP transgenes in control experiments and produced a spectrum of phenotypes very similar to the ehbp-1(tm2523) deletion mutant. These results suggest that loss of EHBP-1, like loss of RAB-10, produces severe defects in basolateral endocytic recycling.

Figure 4.
Loss of EHBP-1 induces endocytic recycling defects in the C. elegans intestine. (A and B) Nomarski images of the intestines in wild-type and ehbp-1(RNAi) animals. Large transparent vacuoles were found in the intestines of ehbp-1(RNAi) animals (B). Arrows ...

Cargo-specific Requirements for EHBP-1

To test the importance and specificity of EHBP-1 in cargo recycling, we assayed the effect of ehbp-1 mutation on well-established recycling cargo proteins hTAC-GFP (CIE marker) and hTfR-GFP (CDE marker) in ehbp-1 mutant animals (Chen et al., 2006 blue right-pointing triangle; Shi et al., 2007 blue right-pointing triangle). We previously found that loss of RAB-10 caused dramatic intracellular accumulation of hTAC-GFP, consistent with a defect in hTAC recycling (Chen et al., 2006 blue right-pointing triangle). Loss of RAB-10 had only minor effects on hTfR-GFP (Chen et al., 2006 blue right-pointing triangle). These results suggested a cargo-specific role for RAB-10 in the recycling pathway.

In ehbp-1(tm2523) mutant animals, hTAC-GFP accumulated dramatically within the intestinal cells in intracellular tubules and enlarged puncta (Figure 4, F and K), very similar to the phenotype observed in rab-10 mutants (Figure 4, G and K). hTfR-GFP localization appeared unperturbed in ehbp-1(tm2523) mutant animals, suggesting that like RAB-10, EHBP-1 affects recycling in a cargo-specific manner (Figure 4, I–K). Consistent with the direct action of EHBP-1 on endosomes transporting hTAC, we found a high degree of colocalization between EHBP-1-mCherry and hTAC-GFP on intracellular tubules and puncta (Supplemental Figure S5, A–A″).

Although overexpression of full-length EHBP-1-mCherry did not overtly affect the localization of hTAC-GFP, we found that overexpression of a truncated form of EHBP-1(aa1–711), lacking the RAB-10–interacting coiled-coil domain, induced dominant negative phenotypes including overaccumulation of intracellular hTAC-GFP and the formation of grossly enlarged intestinal vacuoles similar to those observed in ehbp-1 loss-of-function mutants (Supplemental Figure S5, C–F). Colocalization studies showed that the truncated form of EHBP-1(aa1–711) colocalizes with hTAC-GFP on the accumulated intracellular structures (Supplemental Figure S5, B–B″).

EHBP-1 Is Important for Endosome Morphology

Our previous work indicated that the grossly enlarged endosomes in rab-10 mutants are labeled by the early endosome marker GFP-RAB-5, but not by the basolateral recycling endosome marker GFP-RME-1. In fact, rab-10 mutants extensively overaccumulate GFP-RAB-5 labeled early endosomes of all sizes and display abnormal localization of the recycling endosome marker GFP-RME-1. In rab-10 mutants GFP-RME-1 is more diffusely distributed, with the remaining GFP-RME-1 labeled structures being larger, fewer in number, and displaying a pronounced loss of their normal tubular morphology (Chen et al., 2006 blue right-pointing triangle). ehbp-1 mutants displayed very similar endosomal defects, including increased GFP-RAB-5 labeling and loss of GFP-RME-1–labeled recycling endosome tubular morphology (Figure 5, A–F, quantified in G and H). In contrast, there was no effect on the subcellular localization or number of RAB-11-labeled apical recycling endosomes in ehbp-1 mutants (Supplemental Figure S6).

Figure 5.
Accumulation of RAB-5–positive early endosomes and disrupted RME-1–positive tubular recycling structures in ehbp-1(tm2523) and rab-10(q373) mutants. Representative confocal images are shown for GFP-RAB-5 (A–C) and GFP-RME-1 (D–F). ...

These results suggest that EHBP-1 and RAB-10 function at a similar step in endocytic transport, upstream of RME-1. Consistent with the idea that RME-1 functions downstream of RAB-10, we found that in rme-1(b1045) mutants the average intensity of GFP-RAB-10–labeled endosomes increased by about threefold (Figure 6, A, C, and H). This result suggests a blockage of the recycling pathway downstream of RAB-10 in cells lacking RME-1. We also found that the morphology of EHBP-1-GFP–labeled structures was perturbed in rme-1 mutants. EHBP-1-GFP localization appeared less tubular, with abnormal accumulation in patches and enlarged puncta (Figure 6, D, F, and I). Lack of RME-1 did not appear to affect the association of EHBP-1-GFP with membranes however.

EHBP-1 Controls the Localization of RAB-10

In many cases proteins that interact with GTP-bound Rabs are effector proteins, and such effectors are often localized and/or activated by interaction with the Rab protein (Stenmark, 2009 blue right-pointing triangle). To determine if RAB-10 and EHBP-1 display such a relationship, we assayed for changes in the localization of EHBP-1-GFP in a rab-10 mutant background. In the absence of RAB-10, the morphology of EHBP-1-GFP–labeled structures was perturbed, but EHBP-1 localization to membranes was not significantly affected (Figure 6, D and E, and quantified in I). EHBP-1-GFP localization appeared less tubular, with abnormal accumulation in patches, vacuoles, and enlarged puncta (Figure 6, D and E, and Supplemental Figure S7C). RNAi-mediated knockdown of RAB-8 did not perturb the morphology of EHBP-1-GFP–labeled structures (Supplemental Figure S7B). In addition, rab-8(RNAi) in a rab-10 mutant background did not further disrupt EHBP-1-GFP endosomal morphology or membrane localization beyond that already observed in rab-10 mutants alone (Supplemental Figure S7, C and D). These results suggest that although RAB-10 is important for the morphology of EHBP-1 associated endosomes, neither RAB-10 nor -8 is required for the EHBP-1 endosomal recruitment.

We also performed the converse experiment, testing for changes in GFP-RAB-10 and GFP-RAB-8 localization in animals lacking EHBP-1. Surprisingly, we found that GFP-RAB-10 was much more diffusive in the cytosol of ehbp-1(tm2523) mutants than in control animals (Figure 6, A and B). The intensity of GFP-RAB-10–labeled puncta was reduced by ~20-fold in ehbp-1 mutants (Figure 6H). The increased diffusion and reduced intensity of GFP-RAB-10 endosomal labeling suggests that EHBP-1 functions upstream of RAB-10, promoting the association of RAB-10 with endosomes. Unlike GPP-RAB-10, we found that GFP-RAB-8–labeled structures overaccumulated in ehbp-1(RNAi) animals (Supplemental Figure S8, B and E). Furthermore, GFP-RAB-8–labeled structures also overaccumulated in rab-10(q373) mutants (Supplemental Figure S8, C and E). This behavior of the RAB-8–marked endosomes is very similar to that we observed with RAB-5–labeled endosomes and is the opposite of the observed effect on GFP-RAB-10. These data suggest that neither RAB-8 nor -5 requires EHBP-1 for endosomal recruitment. Rather these results indicate that RAB-8 and -5 are present on the endosomes that overaccumulate in the absence of RAB-10/EHBP-1–dependent recycling.

EHBP-1 Regulates GLR-1 Glutamate Receptor Trafficking

In addition to its role in the intestinal epithelium, C. elegans RAB-10 has also been reported to regulate the endocytic recycling of the AMPA-type glutamate receptor GLR-1, which is localized to synapses and controls the command interneuron circuit that mediates reversal behavior while animals forage (Hart et al., 1995 blue right-pointing triangle; Maricq et al., 1995 blue right-pointing triangle; Glodowski et al., 2007 blue right-pointing triangle). To determine whether, like RAB-10, EHBP-1 has a similar role in GLR-1 trafficking, we introduced a transgene expressing a full-length GLR-1-GFP chimeric protein into ehbp-1 mutants (Rongo et al., 1998 blue right-pointing triangle). In control animals, GLR-1-GFP is localized to small (~0.5 μm) punctate structures that colocalize with other postsynaptic proteins along ventral cord neurites (Figure 7A; Rongo et al., 1998 blue right-pointing triangle; Burbea et al., 2002 blue right-pointing triangle). In both rab-10 and ehbp-1 mutant animals, we found an abnormal accumulation of GLR-1-GFP in elongated (~2–5 μm) accretions along the ventral cord neurites (Figure 7, B and C). These accretions are thought to be receptors trapped in internal compartments, most likely endosomes (Glodowski et al., 2007 blue right-pointing triangle; Chun et al., 2008 blue right-pointing triangle; Park et al., 2009 blue right-pointing triangle). We quantified the magnitude of the effect of rab-10 and ehbp-1 mutations on GLR-1 localization by classifying localized GLR-1-GFP into either small puncta or long accretions based on their size and morphology. Both mutants had elevated numbers of GLR-1 accretions (Figure 7D), with a mean size greater than that found for the rare accretion seen in wild type (Figure 7E). In contrast, ehbp-1 and rab-10 mutants contained fewer than wild-type numbers of small GLR-1-GFP puncta, which are thought to be receptors clustered at postsynaptic elements (Figure 7F; Rongo et al., 1998 blue right-pointing triangle; Burbea et al., 2002 blue right-pointing triangle). In contrast to ehbp-1 and rab-10 mutants, rab-8 mutants displayed only very mild perturbation of GLR-1-GFP puncta and accretion size and displayed normal accretion and puncta number (Supplemental Figure S9, A–F).

Figure 7.
EHBP-1 regulates GLR-1 glutamate receptor trafficking. GLR-1-GFP fluorescence was observed along ventral cord neurites of (A) wild-type animals, (B) rab-10(q373) mutants, and (C) ehbp-1(tm2523) mutants. In wild-type animals, GLR-1-GFP is localized to ...

The change in GLR-1-GFP localization in ehbp-1 mutants could be due to defects in synapse formation. To test this possibility, we introduced a transgene expressing synaptic vesicle marker SNB-1-GFP (synaptobrevin), which labels synaptic terminals in the interneurons, into ehbp-1 mutants (Nonet et al., 1998 blue right-pointing triangle; Rongo et al., 1998 blue right-pointing triangle). The number and distribution of SNB-1-GFP–labeled structures were similar in both wild-type and ehbp-1 mutant animals (Figure 7, G–I), indicating that the observed defects in GLR-1 localization are unlikely to be due to gross defects in synapse formation.

If ehbp-1 mutations prevent the recycling of GLR-1 and instead result in GLR-1 accumulating in internal accretions, then these mutations should result in corresponding GLR-1–mediated behavioral defects (Burbea et al., 2002 blue right-pointing triangle; Glodowski et al., 2007 blue right-pointing triangle). GLR-1 positively regulates spontaneous reversals in locomotion during foraging, and the frequency of these reversals provides a quantitative measure of GLR-1 activity (Zheng et al., 1999 blue right-pointing triangle; Mellem et al., 2002 blue right-pointing triangle). We measured the spontaneous reversal frequency of wild type, glr-1 mutants, rab-10 mutants, ehbp-1 homozygous mutants, and ehbp-1 heterozygotes (30 animals, 5-min trials). As previously described, rab-10 mutants change direction at half the rate of wild-type animals, similar to the rate observed in glr-1 null mutants (Glodowski et al., 2007 blue right-pointing triangle; Figure 7J). Like rab-10 mutants, ehbp-1 mutants reversed direction at a depressed rate. Unlike rab-10 and ehbp-1, rab-8 mutants displayed normal spontaneous reversal frequency (Supplemental Figure S9G).

Taken together, these results indicate that EHBP-1 and RAB-10 regulate the trafficking of GLR-1 from endosomal compartments within the neurites to synaptic membranes, whereas RAB-8 plays little or no role in this process.

As described above, RAB-10 and EHBP-1 can physically interact in vitro. To determine whether EHBP-1 and RAB-10 associate at similar compartments in the ventral cord neurites in vivo, we introduced transgenes that express EHBP-1-GFP and mRFP-RAB-10 in the interneurons via the glr-1 promoter. We found extensive colocalization of EHBP-1-GFP and RFP-RAB-10 along the ventral cord neurites (Figure 7, K–M). These findings indicate that EHBP-1 and RAB-10 are largely present at the same subcellular structures along the ventral cord. Unlike RFP-RAB-10, RFP-RAB-8 was diffusely distributed throughout the neurites and failed to colocalize with GFP-EHBP-1 (Supplemental Figure S9H).

In C. elegans intestinal cells, EHBP-1 regulates RAB-10 subcellular localization. To test for a similar role in neurons, we assayed ehbp-1 mutants for changes in GFP-RAB-10 localization in interneurons. Although GFP-RAB-10 is localized at both large accretions and small punctae along the ventral nerve cord in control animals (Figure 7N), GFP-RAB-10 is only localized to small puncta in ehbp-1 mutants (Figure 7O). In ehbp-1 mutant animals, the average number of GFP-RAB-10–containing accretions was reduced dramatically (approximately sixfold lower than that in control animals; Figure 7P), and the mean size of the accretions was also reduced (Figure 7Q). The number of small GFP-RAB-10 puncta remained the same (Figure 7R). Taken together, these results indicate that, similar to what was observed in the intestinal cells, EHBP-1 regulates the subcellular localization of RAB-10 in neurons.

EHBP-1 Is Required in the Germline

As mentioned earlier, we found that adult ehbp-1(tm2523) mutant animals are completely sterile (0 eggs produced, n = 18 adult hermaphrodites). The sterile adults have abnormally small gonads and completely lack the characteristic row of large squared-off oocyte cells in the proximal gonad region (Figure 8, A and E, arrows). This suggests a defect in oocyte growth and/or differentiation in these animals. Although such a phenotype might be explained by severe membrane-trafficking defects in the germline cells, this phenotype cannot be completely explained simply by loss of RAB-10 or -8 function, because neither the rab-10 nor -8 mutant is sterile; however, each single mutant does display a reduced brood size. We measured rab-10 mutant brood size as 162 ± 10 (n = 18) and rab-8 mutant brood size as 152 ± 4 (n = 18), compared with wild-type N2 controls that displayed a brood size of 280 ± 12 (n = 18).

Figure 8.
(A–E) Nomarski images of the gonads in wild-type, rab-10(q373), rab-8(RNAi), rab-10(q373);rab-8(RNAi), and ehbp-1(tm2523) animals. Developmental defects of gonads were found in rab-10(q373);rab-8(RNAi) animals and ehbp-1(tm2523) mutants (D and ...

Thus we sought to determine if the sterile phenotype might be explained by loss of RAB-8 function, in addition to RAB-10 function, in the ehbp-1 mutant germ cells. This was suggested by the findings that EHBP-1 can physically interact with RAB-8 in addition to RAB-10, that RAB-8 and -10 are very similar to each other at the sequence level, and previous RNAi evidence that RAB-8 and -10 possess an essential overlapping function in the germline (Audhya et al., 2007 blue right-pointing triangle). There have also been suggestions of redundancy in this Rab pair in mammalian MDCK cells (Schuck et al., 2007 blue right-pointing triangle). Thus we compared the germline phenotype of ehbp-1 mutants with that of animals depleted of RAB-8 or of animals depleted of both RAB-8 and -10. We found that although RNAi-mediated depletion of RAB-8 did not produce sterility in an otherwise wild-type background, RNAi-mediated depletion of RAB-8 in a rab-10 mutant background produced sterile adult phenotypes that strongly resembled ehbp-1 mutant animals (Figure 8, D and E, and Supplemental Figure S10, arrows).

Given the poor growth of the germline, and the abnormal oocytes in particular, the typical assay used to measure endocytic transport in the germline—uptake of GFP-tagged yolk proteins by oocytes—did not appear appropriate. In addition, our previous work indicated that oocytes of nearly normal size are produced in animals with severe defects in oocyte endocytosis, whereas defects in secretion frequently lead to small and abnormal oocytes (Grant and Hirsh, 1999 blue right-pointing triangle; Balklava et al., 2007 blue right-pointing triangle). To identify the underlying defect we focused on the oocyte precursors located between the transition zone and the bend in the gonad arm, assaying effects of loss of EHBP-1, RAB-10, and/or RAB-8 on the localization of a secreted transmembrane SNARE protein, SNB-1 (boxed region in the diagram, Supplemental Figure S11). Although SNB-1 is best known as a neuronal protein found mainly found in synaptic vesicles, it is also normally expressed in the germline (Sato et al., 2008a blue right-pointing triangle). At steady state, GFP-SNB-1, like endogenous SNB-1 (Sato et al., 2008a blue right-pointing triangle), localized mostly to the plasma membrane of developing compartments in the germline, although a subpopulation could also be found on punctate structures that likely correspond to secretory vesicles and endosomes (Figure 8F′ and data not shown). The accumulation of GFP-SNB-1 on the plasma membrane was confirmed by colocalization studies with an mCherry fusion to the PH domain derived from rat PLC1δ, which binds specifically to the plasma membrane-localized lipid, phosphatidylinositol 4,5-bisphosphate (Figure 8, F–F″). Line-scan analysis showed that the fluorescence intensities of GFP-SNB-1 and mCherry-PH peaked at identical points, illustrating a high degree of colocalization (Figure 8F[triple prime]). Codepletion of RAB-8 and -10 caused a striking defect in the accumulation of GFP-SNB-1 at the plasma membrane. Instead, the SNARE protein accumulated almost exclusively on internal punctate structures and failed to colocalize with the plasma membrane mCherry-PH marker (Figure 8, G–G[triple prime]). Depletion of EHBP-1 caused a similar defect in GFP-SNB-1 transport to the plasma membrane (Figure 8, H–H[triple prime]). Taken together, these results indicate that RAB-8 and -10 function redundantly in the secretory pathway of C. elegans germ cells and further suggest that EHBP-1 functions with RAB-8 and -10 in this process.


Here we present the first functional studies of ehbp-1 mutant animals and demonstrate an important relationship between EHBP-1 with RAB-10 during endocytic recycling. We show that a predicted coiled-coil domain in the C-terminus of EHBP-1 binds directly to active GTP-bound RAB-10, that a functional EHBP-1-GFP fusion protein colocalizes with RFP-RAB-10 in epithelial cells and neurons, and that animals lacking EHBP-1 or RAB-10 share a specific set of endosomal defects, miss-sort cargo proteins in a similar manner, and display similar defects in organismal behavior. The RAB-10-like phenotypes found in ehbp-1 mutants appear to result from a failure to efficiently recruit RAB-10 to endosomal membranes. However, in some respects, loss of EHBP-1 more severely impacts C. elegans development as compared with the loss of RAB-10, more closely resembling the defects found in animals lacking both RAB-10 and RAB-8, to which EHBP-1 can also bind.

The finding that EHBP-1 is important for RAB-10 membrane recruitment is unexpected, because EHBP-1 appears to interact with the GTP-bound form of RAB-10. Membrane recruitment of Rabs is most commonly associated with Rab guanine nucleotide exchange factors (GEFs), but GEFs interact with the GDP-bound or nucleotide-free forms of the Rab and promote GDP/GTP exchange. Proteins that bind to GTP-bound Rabs are typically thought of as Rab effectors, and Rab effectors are typically recruited to the membrane by the Rab GTPase, and not vice versa as was observed in this case. However, there is an interesting recent precedent for this type of interaction. While this manuscript was in preparation, an article by Sharma et al. (2009) blue right-pointing triangle showed that mammalian MICAL-L1, identified as a Rab8(GTP) binding partner, functions as an upstream regulator of Rab8 that is important for the association of Rab8 with endosomal membranes. This study is also particularly relevant because MICAL-L1 has a domain structure somewhat similar to EHBP-1, including a central CH-domain and a C-terminal Rab-binding domain predicted to adopt a coiled-coil structure. Mammalian cells express Ehbp1 in addition to several different MICAL proteins, and the MICAL proteins all engage various members of the Rab10/Rab8/Rab13 family to promote endocytic transport (Weide et al., 2003 blue right-pointing triangle; Yamamura et al., 2008 blue right-pointing triangle). EHBP-1 appears to be the only C. elegans protein bearing a similar domain structure to mammalian Ehbp1 and MICAL-L1 in the predicted worm proteome.

Mammalian Ehbp1 was originally identified in NIH3T3 cells as a binding partner of EHD1 and EHD2, members of the RME-1 family of ATPases (Guilherme et al., 2004a blue right-pointing triangle; Guilherme et al., 2004b blue right-pointing triangle). Likewise, MICAL-L1 was recently shown to bind to EHD1 (Sharma et al., 2009 blue right-pointing triangle). Mammalian Ehbp1 and MICAL-L1 contain N-terminal NPF sequences that bind to the C-terminal EH-domain of the EHD proteins. RME-1/EHD family proteins are ATPases that are thought to function as membrane tubulation and/or fission molecules on endosomes, possibly functioning in a manner analogous to the well-studied fission regulator Dynamin (Daumke et al., 2007 blue right-pointing triangle; Grant and Caplan, 2008 blue right-pointing triangle; Pant et al., 2009 blue right-pointing triangle). The direct association of EHBP-1/MICAL-L1-type proteins with RME-1/EHDs does not appear to be evolutionarily conserved, however, because C. elegans EHBP-1 lacks NPF sequences, and we could not detect a physical interaction between RME-1 with EHBP-1. Rather, EHBP-1's effects on RME-1 localization appears to be indirect, mediated through regulation of RAB-10. EHBP-1 and RAB-10 function upstream of RME-1 at the basolateral early and/or recycling endosome in intestinal cells, affecting RME-1 localization to tubular membranes of the recycling endosome.

It is also interesting to note that in the 3T3 adipocyte model, siRNA-mediated depletion of Ehbp1 abolished the insulin-regulated endosome to plasma membrane transport of the glucose transporter Glut4 (Guilherme et al., 2004b blue right-pointing triangle). Because mammalian Rab10 (in adipocytes) and mammalian Rab8 (in muscle cells) are now known to be important for Glut4 recycling in response to an insulin signal (Sano et al., 2007 blue right-pointing triangle; Randhawa et al., 2008 blue right-pointing triangle), it is reasonable to suspect that mammalian Ehbp1 might mediate its effects on Glut4 via interaction with Rab10 and/or Rab8.

In our study, we showed that EHBP-1 also physically interacts with RAB-8 in vitro and colocalizes with RAB-8 in vivo. Nevertheless, we noticed significant phenotypic differences upon loss of RAB-10 or -8 in various tissues. For instance, depletion of RAB-10 strongly affects EHBP-1 labeled endosome morphology in the polarized intestinal cells, an effect not seen upon knockdown of RAB-8 (Supplemental Figure S7). Likewise, loss of RAB-8 has very mild effects on GLR-1 localization in interneurons and has no effect on GLR-1–mediated behavior (Supplemental Figure S9, A–G). By contrast, in the nonpolarized germline cells, SNB-1 delivery to the PM was disrupted only upon simultaneous loss of RAB-10 and -8; no defect was observed upon loss of only one of these Rabs. These apparent tissue-specific differences in Rab function may have broader implications. Nonpolarized cells, such as oocytes, may have generally greater redundancy within their endocytic recycling pathways compared with polarized cells such as those of the intestine or nervous system. The increased complexity of basolateral versus apical, or dendritic versus axonal, transport in polarized cells may require greater specialization, and thus perhaps less redundancy, in such pathways. A recent study in the mouse suggested that Rab8 is important for apical transport in polarized enterocytes and also suggested that the same may be true of C. elegans RAB-8 (Sato et al., 2007 blue right-pointing triangle). This is also interesting in light of recent work indicating a Rab11/Rab8 cascade in cilia formation (Knodler et al., 2010 blue right-pointing triangle) and the known preference of Rab11 for apical recycling in polarized epithelia (Casanova et al., 1999 blue right-pointing triangle; Brown et al., 2000 blue right-pointing triangle). Thus one possibility is that in polarized cells like the intestinal enterocytes, RAB-8 and -10 function differentially in apical versus basolateral recycling, whereas in nonpolarized cells such as oocytes both pathways exist but function redundantly.

Rab family GTPases have been shown to function in the generation, maintenance, and membrane trafficking processes of intracellular compartments (Stenmark, 2009 blue right-pointing triangle). Different Rab GTPases can coexist on the same compartment in distinct subdomains, and in some cases Rab cascades have been proposed (Sonnichsen et al., 2000 blue right-pointing triangle; Ortiz et al., 2002 blue right-pointing triangle). For instance Rab5 is thought to recruit activators of Rab7 to the endosome during endosome maturation, promoting entry of cargo into the degradative compartment and recycling of retromer-dependent cargo to the Golgi (Rink et al., 2005 blue right-pointing triangle). However, Rab5 also interacts with the recycling machinery that promotes transport to recycling endosomes. For instance, Rab5 binds to Rabenosyn-5, a protein that also interacts with recycling associated proteins Rab4 and EHD1 (Naslavsky et al., 2004 blue right-pointing triangle, 2006 blue right-pointing triangle). In vitro, we observed a weak binding of EHBP-1 to RAB-5, albeit not as strong an interaction as was found with RAB-10 or -8. Interestingly, we observed that RNAi-mediated knockdown of RAB-5 resulted in poor recruitment of EHBP-1 to endosomal membranes (Figure 6, G and I). Conversely, loss of EHBP-1 caused the abnormally high accumulation of GFP-RAB-5, in parallel with a defect in proper recruitment of RAB-10. Thus, one possibility is that EHBP-1 interacts with RAB-5 and -10 sequentially, acting to promote the exchange of RAB-5 for RAB-10 on endosomes as they mature along the recycling pathway. Further analysis will be required to substantiate such a model.

The CH-domain of EHBP-1 is also interesting with regard to endosome function, as CH-domains are thought to interact with cytoskeletal elements. Classically CH-domains are thought to be actin-interaction modules, although recent work suggests that in some proteins CH-domains can interact with microtubules (Sjoblom et al., 2008 blue right-pointing triangle). Actin in particular is important for the recycling of CIE cargo such as TAC and MHCI, and EHBP-1 and RAB-10 are preferentially involved in the recycling of such cargo (Radhakrishna and Donaldson, 1997 blue right-pointing triangle; Weigert et al., 2004 blue right-pointing triangle). Future analysis will be focused on determining if EHBP-1 helps to connect endosomes to cytoskeletal networks to promote endocytic recycling function.

Supplementary Material

[Supplemental Materials]


We thank Yuji Kohara (National Institute of Genetics, Japan) and Shohei Mitani (Tokyo Women's Medical University) for important reagents, and we thank Karen Oegema (Ludwig Institute for Cancer Research, San Diego, CA) for generously providing unpublished marker strains for this study. We thank Saumya Pant, Peter Schweinsberg, and Zui Pan for their generous advice and technical assistance. R.B. was supported by Aresty Research Center grant. This work was supported by National Institutes of Health (NIH) R01 NS42023 to C.R. This work was supported by NIH Grant GM067237 to B.D.G.


This article was published online ahead of print in MBoC in Press ( on June 23, 2010.


  • Allaire P. D., Marat A. L., Dall'Armi C., Di Paolo G., McPherson P. S., Ritter B. The Connecdenn DENN domain: a GEF for Rab35 mediating cargo-specific exit from early endosomes. Mol. Cell. 2010;37:370–382. [PMC free article] [PubMed]
  • Ang A. L., Folsch H., Koivisto U. M., Pypaert M., Mellman I. The Rab8 GTPase selectively regulates AP-1B-dependent basolateral transport in polarized Madin-Darby canine kidney cells. J. Cell Biol. 2003;163:339–350. [PMC free article] [PubMed]
  • Ang A. L., Taguchi T., Francis S., Folsch H., Murrells L. J., Pypaert M., Warren G., Mellman I. Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells. J. Cell Biol. 2004;167:531–543. [PMC free article] [PubMed]
  • Audhya A., Desai A., Oegema K. A role for Rab5 in structuring the endoplasmic reticulum. J. Cell Biol. 2007;178:43–56. [PMC free article] [PubMed]
  • Babbey C. M., Ahktar N., Wang E., Chen C. C., Grant B. D., Dunn K. W. Rab10 regulates membrane transport through early endosomes of polarized Madin-Darby canine kidney cells. Mol. Biol. Cell. 2006;17:3156–3175. [PMC free article] [PubMed]
  • Balklava Z., Pant S., Fares H., Grant B. D. Genome-wide analysis identifies a general requirement for polarity proteins in endocytic traffic. Nat. Cell Biol. 2007;9:1066–1073. [PubMed]
  • Brenner S. The genetics of Caenorhabditis elegans. Genetics. 1974;77:71–94. [PubMed]
  • Brown P. S., Wang E., Aroeti B., Chapin S. J., Mostov K. E., Dunn K. W. Definition of distinct compartments in polarized Madin-Darby canine kidney (MDCK) cells for membrane-volume sorting, polarized sorting and apical recycling. Traffic. 2000;1:124–140. [PubMed]
  • Burbea M., Dreier L., Dittman J. S., Grunwald M. E., Kaplan J. M. Ubiquitin and AP180 regulate the abundance of GLR-1 glutamate receptors at postsynaptic elements in C. elegans. Neuron. 2002;35:107–120. [PubMed]
  • Casanova J. E., Wang X., Kumar R., Bhartur S. G., Navarre J., Woodrum J. E., Altschuler Y., Ray G. S., Goldenring J. R. Association of Rab25 and Rab11a with the apical recycling system of polarized Madin-Darby canine kidney cells. Mol. Biol. Cell. 1999;10:47–61. [PMC free article] [PubMed]
  • Cheeseman I. M., Niessen S., Anderson S., Hyndman F., Yates J. R., 3rd, Oegema K., Desai A. A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension. Genes Dev. 2004;18:2255–2268. [PubMed]
  • Chen C. C., Schweinsberg P. J., Vashist S., Mareiniss D. P., Lambie E. J., Grant B. D. RAB-10 is required for endocytic recycling in the Caenorhabditis elegans intestine. Mol. Biol. Cell. 2006;17:1286–1297. [PMC free article] [PubMed]
  • Chun D. K., McEwen J. M., Burbea M., Kaplan J. M. UNC-108/Rab2 regulates postendocytic trafficking in Caenorhabditis elegans. Mol. Biol. Cell. 2008;19:2682–2695. [PMC free article] [PubMed]
  • Clokey G. V., Jacobson L. A. The autofluorescent “lipofuscin granules” in the intestinal cells of Caenorhabditis elegans are secondary lysosomes. Mech. Ageing Dev. 1986;35:79–94. [PubMed]
  • Daumke O., Lundmark R., Vallis Y., Martens S., Butler P. J., McMahon H. T. Architectural and mechanistic insights into an EHD ATPase involved in membrane remodelling. Nature. 2007;449:923–927. [PubMed]
  • Fares H., Greenwald I. Genetic analysis of endocytosis in Caenorhabditis elegans: coelomocyte uptake defective mutants. Genetics. 2001;159:133–145. [PubMed]
  • Gesbert F., Sauvonnet N., Dautry-Varsat A. Clathrin-independent endocytosis and signalling of interleukin 2 receptors IL-2R endocytosis and signalling. Curr. Top. Microbiol. Immunol. 2004;286:119–148. [PubMed]
  • Glodowski D. R., Chen C. C., Schaefer H., Grant B. D., Rongo C. RAB-10 regulates glutamate receptor recycling in a cholesterol-dependent endocytosis pathway. Mol. Biol. Cell. 2007;18:4387–4396. [PMC free article] [PubMed]
  • Grant B., Hirsh D. Receptor-mediated endocytosis in the Caenorhabditis elegans oocyte. Mol. Biol. Cell. 1999;10:4311–4326. [PMC free article] [PubMed]
  • Grant B. D., Caplan S. Mechanisms of EHD/RME-1 protein function in endocytic transport. Traffic. 2008;9:2043–2052. [PMC free article] [PubMed]
  • Grant B. D., Donaldson J. G. Pathways and mechanisms of endocytic recycling. Nat. Rev. Mol. Cell Biol. 2009;10:597–608. [PMC free article] [PubMed]
  • Grosshans B. L., Ortiz D., Novick P. Rabs and their effectors: achieving specificity in membrane traffic. Proc. Natl. Acad. Sci. USA. 2006;103:11821–11827. [PubMed]
  • Guilherme A., Soriano N. A., Bose S., Holik J., Bose A., Pomerleau D. P., Furcinitti P., Leszyk J., Corvera S., Czech M. P. EHD2 and the novel EH domain binding protein EHBP1 couple endocytosis to the actin cytoskeleton. J. Biol. Chem. 2004a;279:10593–10605. [PubMed]
  • Guilherme A., Soriano N. A., Furcinitti P. S., Czech M. P. Role of EHD1 and EHBP1 in perinuclear sorting and insulin-regulated GLUT4 recycling in 3T3–L1 adipocytes. J. Biol. Chem. 2004b;279:40062–40075. [PubMed]
  • Hart A. C., Sims S., Kaplan J. M. Synaptic code for sensory modalities revealed by C. elegans GLR-1 glutamate receptor. Nature. 1995;378:82–84. [PubMed]
  • Hattula K., Furuhjelm J., Arffman A., Peranen J. A Rab8-specific GDP/GTP exchange factor is involved in actin remodeling and polarized membrane transport. Mol. Biol. Cell. 2002;13:3268–3280. [PMC free article] [PubMed]
  • Hattula K., Furuhjelm J., Tikkanen J., Tanhuanpaa K., Laakkonen P., Peranen J. Characterization of the Rab8-specific membrane traffic route linked to protrusion formation. J. Cell Sci. 2006;119:4866–4877. [PubMed]
  • Henry L., Sheff D. R. Rab8 regulates basolateral secretory, but not recycling, traffic at the recycling endosome. Mol. Biol. Cell. 2008;19:2059–2068. [PMC free article] [PubMed]
  • Hermann G. J., Schroeder L. K., Hieb C. A., Kershner A. M., Rabbitts B. M., Fonarev P., Grant B. D., Priess J. R. Genetic analysis of lysosomal trafficking in Caenorhabditis elegans. Mol. Biol. Cell. 2005;16:3273–3288. [PMC free article] [PubMed]
  • Kachur T. M., Audhya A., Pilgrim D. B. UNC-45 is required for NMY-2 contractile function in early embryonic polarity establishment and germline cellularization in. C. elegans. Dev. Biol. 2008;314:287–299. [PubMed]
  • Kamath R. S., Ahringer J. Genome-wide RNAi screening in Caenorhabditis elegans. Methods. 2003;30:313–321. [PubMed]
  • Knodler A., Feng S., Zhang J., Zhang X., Das A., Peranen J., Guo W. Coordination of Rab8 and Rab11 in primary ciliogenesis. Proc. Natl. Acad. Sci. USA. 2010;107:6346–6351. [PubMed]
  • Kouranti I., Sachse M., Arouche N., Goud B., Echard A. Rab35 regulates an endocytic recycling pathway essential for the terminal steps of cytokinesis. Curr. Biol. 2006;16:1719–1725. [PubMed]
  • Maricq A. V., Peckol E., Driscoll M., Bargmann C. I. Mechanosensory signalling in C. elegans mediated by the GLR-1 glutamate receptor. Nature. 1995;378:78–81. [PubMed]
  • Maxfield F. R., McGraw T. E. Endocytic recycling. Nat. Rev. Mol. Cell Biol. 2004;5:121–132. [PubMed]
  • Mellem J. E., Brockie P. J., Zheng Y., Madsen D. M., Maricq A. V. Decoding of polymodal sensory stimuli by postsynaptic glutamate receptors in C. elegans. Neuron. 2002;36:933–944. [PubMed]
  • Mukherjee S., Ghosh R. N., Maxfield F. R. Endocytosis. Physiol. Rev. 1997;77:759–803. [PubMed]
  • Naslavsky N., Boehm M., Backlund P. S., Jr, Caplan S. Rabenosyn-5 and EHD1 interact and sequentially regulate protein recycling to the plasma membrane. Mol. Biol. Cell. 2004;15:2410–2422. [PMC free article] [PubMed]
  • Naslavsky N., Rahajeng J., Sharma M., Jovic M., Caplan S. Interactions between EHD proteins and Rab11-FIP2, a role for EHD3 in early endosomal transport. Mol. Biol. Cell. 2006;17:163–177. [PMC free article] [PubMed]
  • Nichols B. Caveosomes and endocytosis of lipid rafts. J. Cell Sci. 2003;116:4707–4714. [PubMed]
  • Nonet M. L., Saifee O., Zhao H., Rand J. B., Wei L. Synaptic transmission deficits in Caenorhabditis elegans synaptobrevin mutants. J. Neurosci. 1998;18:70–80. [PubMed]
  • Oegema K., Desai A., Rybina S., Kirkham M., Hyman A. A. Functional analysis of kinetochore assembly in Caenorhabditis elegans. J. Cell Biol. 2001;153:1209–1226. [PMC free article] [PubMed]
  • Ortiz D., Medkova M., Walch-Solimena C., Novick P. Ypt32 recruits the Sec4p guanine nucleotide exchange factor, Sec2p, to secretory vesicles; evidence for a Rab cascade in yeast. J. Cell Biol. 2002;157:1005–1015. [PMC free article] [PubMed]
  • Pant S., Sharma M., Patel K., Caplan S., Carr C. M., Grant B. D. AMPH-1/Amphiphysin/Bin1 functions with RME-1/Ehd1 in endocytic recycling. Nat. Cell Biol. 2009;11:1399–1410. [PMC free article] [PubMed]
  • Park E. C., Glodowski D. R., Rongo C. The ubiquitin ligase RPM-1 and the p38 MAPK PMK-3 regulate AMPA receptor trafficking. PLoS ONE. 2009;4:e4284. [PMC free article] [PubMed]
  • Patton A., Knuth S., Schaheen B., Dang H., Greenwald I., Fares H. Endocytosis function of a ligand-gated ion channel homolog in Caenorhabditis elegans. Curr. Biol. 2005;15:1045–1050. [PubMed]
  • Pereira-Leal J. B., Seabra M. C. Evolution of the Rab family of small GTP-binding proteins. J. Mol. Biol. 2001;313:889–901. [PubMed]
  • Powelka A. M., Sun J., Li J., Gao M., Shaw L. M., Sonnenberg A., Hsu V. W. Stimulation-dependent recycling of integrin beta1 regulated by ARF6 and Rab11. Traffic. 2004;5:20–36. [PubMed]
  • Praitis V., Casey E., Collar D., Austin J. Creation of low-copy integrated transgenic lines in Caenorhabditis elegans. Genetics. 2001;157:1217–1226. [PubMed]
  • Radhakrishna H., Donaldson J. G. ADP-ribosylation factor 6 regulates a novel plasma membrane recycling pathway. J. Cell Biol. 1997;139:49–61. [PMC free article] [PubMed]
  • Randhawa V. K., Ishikura S., Talior-Volodarsky I., Cheng A. W., Patel N., Hartwig J. H., Klip A. GLUT4 vesicle recruitment and fusion are differentially regulated by Rac, AS160, and Rab8A in muscle cells. J. Biol. Chem. 2008;283:27208–27219. [PubMed]
  • Rink J., Ghigo E., Kalaidzidis Y., Zerial M. Rab conversion as a mechanism of progression from early to late endosomes. Cell. 2005;122:735–749. [PubMed]
  • Rojas R., Kametaka S., Haft C. R., Bonifacino J. S. Interchangeable but essential functions of SNX1 and SNX2 in the association of retromer with endosomes and the trafficking of mannose 6-phosphate receptors. Mol. Cell. Biol. 2007;27:1112–1124. [PMC free article] [PubMed]
  • Rongo C., Whitfield C. W., Rodal A., Kim S. K., Kaplan J. M. LIN-10 is a shared component of the polarized protein localization pathways in neurons and epithelia. Cell. 1998;94:751–759. [PubMed]
  • Sano H., Eguez L., Teruel M. N., Fukuda M., Chuang T. D., Chavez J. A., Lienhard G. E., McGraw T. E. Rab10, a target of the AS160 Rab GAP, is required for insulin-stimulated translocation of GLUT4 to the adipocyte plasma membrane. Cell Metab. 2007;5:293–303. [PubMed]
  • Sato M., Grant B. D., Harada A., Sato K. Rab11 is required for synchronous secretion of chondroitin proteoglycans after fertilization in Caenorhabditis elegans. J. Cell Sci. 2008a;121:3177–3186. [PubMed]
  • Sato M., Sato K., Fonarev P., Huang C. J., Liou W., Grant B. D. Caenorhabditis elegans RME-6 is a novel regulator of RAB-5 at the clathrin-coated pit. Nat. Cell Biol. 2005;7:559–569. [PMC free article] [PubMed]
  • Sato M., Sato K., Liou W., Pant S., Harada A., Grant B. D. Regulation of endocytic recycling by C. elegans Rab35 and its regulator RME-4, a coated-pit protein. EMBO J. 2008b;27:1183–1196. [PubMed]
  • Sato T., et al. The Rab8 GTPase regulates apical protein localization in intestinal cells. Nature. 2007;448:366–369. [PubMed]
  • Schuck S., Gerl M. J., Ang A., Manninen A., Keller P., Mellman I., Simons K. Rab10 is involved in basolateral transport in polarized Madin-Darby canine kidney cells. Traffic. 2007;8:47–60. [PubMed]
  • Sharma M., Giridharan S. S., Rahajeng J., Naslavsky N., Caplan S. MICAL-L1 links EHD1 to tubular recycling endosomes and regulates receptor recycling. Mol. Biol. Cell. 2009;20:5181–5194. [PMC free article] [PubMed]
  • Shi A., Pant S., Balklava Z., Chen C. C., Figueroa V., Grant B. D. A novel requirement for C. elegans Alix/ALX-1 in RME-1-mediated membrane transport. Curr. Biol. 2007;17:1913–1924. [PMC free article] [PubMed]
  • Sjoblom B., Ylanne J., Djinovic-Carugo K. Novel structural insights into F-actin-binding and novel functions of calponin homology domains. Curr. Opin. Struct. Biol. 2008;18:702–708. [PubMed]
  • Sonnichsen B., De Renzis S., Nielsen E., Rietdorf J., Zerial M. Distinct membrane domains on endosomes in the recycling pathway visualized by multicolor imaging of Rab4, Rab5, and Rab11. J. Cell Biol. 2000;149:901–914. [PMC free article] [PubMed]
  • Stenmark H. Rab GTPases as coordinators of vesicle traffic. Nat. Rev. Mol. Cell Biol. 2009;10:513–525. [PubMed]
  • Timmons L., Fire A. Specific interference by ingested dsRNA. Nature. 1998;395:854. [PubMed]
  • van der Sluijs P., Hull M., Webster P., Male P., Goud B., Mellman I. The small GTP-binding protein rab4 controls an early sorting event on the endocytic pathway. Cell. 1992;70:729–740. [PubMed]
  • Walseng E., Bakke O., Roche P. A. Major histocompatibility complex class II-peptide complexes internalize using a clathrin- and dynamin-independent endocytosis pathway. J. Biol. Chem. 2008;283:14717–14727. [PMC free article] [PubMed]
  • Weide T., Teuber J., Bayer M., Barnekow A. MICAL-1 isoforms, novel rab1 interacting proteins. Biochem. Biophys. Res. Commun. 2003;306:79–86. [PubMed]
  • Weigert R., Yeung A. C., Li J., Donaldson J. G. Rab22a regulates the recycling of membrane proteins internalized independently of clathrin. Mol. Biol. Cell. 2004;15:3758–3770. [PMC free article] [PubMed]
  • Yamamura R., Nishimura N., Nakatsuji H., Arase S., Sasaki T. The interaction of JRAB/MICAL-L2 with Rab8 and Rab13 coordinates the assembly of tight junctions and adherens junctions. Mol. Biol. Cell. 2008;19:971–983. [PMC free article] [PubMed]
  • Zheng Y., Brockie P. J., Mellem J. E., Madsen D. M., Maricq A. V. Neuronal control of locomotion in C. elegans is modified by a dominant mutation in the GLR-1 ionotropic glutamate receptor. Neuron. 1999;24:347–361. [PubMed]

Articles from Molecular Biology of the Cell are provided here courtesy of American Society for Cell Biology