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Localization of nanos (nos) mRNA to the posterior pole of the Drosophila oocyte is essential for abdominal segmentation and germline development during embryogenesis. Posterior localization is mediated by a complex cis-acting localization signal in the nos 3′ untranslated region that comprises multiple partially redundant elements. Genetic analysis suggests that this signal is recognized by RNA-binding proteins and associated factors that package nos mRNA into a localization competent ribonucleoprotein complex. However, functional redundancy among localization elements has made the identification of individual localization factors difficult. Indeed, only a single direct-acting nos localization factor, Rumpelstiltskin (Rump), has been identified thus far. Through a sensitized genetic screen, we have now identified the Argonaute family member Aubergine (Aub) as a nos localization factor. Aub interacts with nos mRNA in vivo and co-purifies with Rump in an RNA-dependent manner. Our results support a role for Aub, independent of its function in RNA silencing, as a component of a nos mRNA localization complex.
mRNA localization is a widespread mechanism used to achieve intracellular polarity in diverse cellular and developmental contexts. Over 1500 transcripts are localized to multiple distinct subcellular locations in the early Drosophila embryo alone, representing approximately 70% of all mRNAs expressed at this time (Lecuyer et al., 2007). Thus, developmental processes require that localized mRNAs be distinguished not only from uniformly distributed transcripts, but also from mRNAs destined for other subcellular locations.
Four localized mRNAs involved in axial patterning within the Drosophila oocyte - gurken (grk), bicoid (bcd), oskar (osk) and nanos (nos) - have established a paradigm for studying the localization of different transcripts to distinct regions within a cell. All four are maternal mRNAs that are synthesized by the ovarian nurse cells, then transported into the oocyte through connecting cytoplasmic channels. During midoogenesis, grk mRNA is localized to the dorsal-anterior region of the oocyte, where it is translated to produce a TGFα-like ligand that signals to overlying somatic follicle cells to establish the dorsoventral (D-V) axis (Neuman-Silberberg and Schüpbach, 1993). Concurrently, osk mRNA localizes to the posterior pole, where its translation is activated. Production of Osk protein is required to maintain osk mRNA and protein localization and to initiate the assembly of the germ plasm, a specialized cytoplasm containing determinants for germ cell formation and, ultimately, nos mRNA (Ephrussi et al., 1991; Kim-Ha et al., 1991; Rongo et al., 1995; Vanzo and Ephrussi, 2002). Transport of grk and osk mRNAs to their destinations is mediated respectively by dynein and kinesin motors and relies on the polarization of the oocyte microtubule cytoskeleton that occurs earlier in oogenesis (reviewed in Becalska and Gavis, 2009).
Although some bcd mRNA is localized to the anterior margin of the oocyte during midoogenesis, the majority does not localize until late stages of oogenesis, after the nurse cells have initiated apoptosis and extruded or “dumped” their contents into the oocyte (Berleth et al., 1988; Weil et al., 2006). It is also during this late phase of oogenesis that nos accumulates within the germ plasm at the oocyte posterior (Forrest and Gavis, 2003). Whereas bcd transport is dynein-dependent, nos is localized passively, being dispersed throughout the oocyte by the concerted streaming of the ooplasm that follows nurse cell dumping, and trapped at the posterior by association with the germ plasm (Forrest and Gavis, 2003; Weil et al., 2006). Localized bcd and nos mRNAs function subsequently during embryogenesis to pattern the anterior-posterior (A-P) axis, through the production of protein gradients that emanate from the anterior and posterior poles respectively. Bcd specifies the development of head and thoracic structures, and mutations that compromise Bcd activity or localization disrupt anterior patterning (Driever and Nüsslein-Volhard, 1988). Nos function is required at the posterior of the embryo for the formation of the eight abdominal segments of the animal, and mutation of nos, or disruption of nos mRNA localization, results in decreased abdominal segmentation (Lehmann and Nusslein-Volhard, 1991; Wang et al., 1994).
The information regulating the specificity of mRNA localization is contained in cis-acting localization elements, typically found in the 3′ untranslated regions (3′UTRs) of localized transcripts (Gavis et al., 2007). These sequences are recognized by trans-acting localization factors that are thought to recruit additional proteins to package mRNAs into ribonucleoprotein (RNP) particles for transport to and anchoring at target destinations. A number of localization factors have been identified for bcd, osk and grk mRNAs (Kugler and Lasko, 2009) but much less is known about the trans-acting factors involved in nos mRNA localization. Traditional genetic screens have been unsuccessful in identifying nos mRNA localization factors due to the complex organization of the nos localization signal. The nos 3′UTR contains four localization elements that play partially redundant roles in nos localization (Gavis et al., 1996). The lack of sequence or structural similarity between the nos localization elements suggests that each is recognized by distinct localization factors that act in combination to mediate localization (Bergsten and Gavis, 1999). However, because no single element is necessary or sufficient for wild-type localization, eliminating a single localization factor is unlikely to result in a phenotypically detectable nos localization defect. Supporting this idea, mutations in the two identified nos localization factors, Rumpelstiltskin (Rump) and Hsp90 cause minimal defects in nos accumulation at the posterior pole (Jain and Gavis, 2008; Song et al., 2007). Rump was identified biochemically by its ability to bind directly to the nos localization signal; however, its requirement in nos mRNA localization is only revealed when the nos localization signal itself is compromised by deletion of two localization elements (Jain and Gavis, 2008). Hsp90 was identified in a dominant modifier screen for nos localization factors using a similar compromised localization signal and, like Rump, its requirement in nos localization is only apparent under these sensitized conditions (Song et al., 2007). How directly Hsp90 regulates nos localization remains unknown.
Here we describe the results of a new sensitized genetic screen for additional nos localization factors and demonstrate that the repeat-associated small interfering RNA (rasiRNA) pathway gene aubergine (aub) plays a role in spatial restriction of nos mRNA. While aub has previously been implicated in localization of osk mRNA (Cook et al., 2004; Wilson et al., 1996), we show that the effect of aub on nos mRNA localization is independent of its upstream effect on osk and the rasiRNA pathway. Furthermore, we demonstrate in vivo interactions between Aub, nos mRNA, and Rump, implicating Aub directly as a novel nos mRNA localization factor.
The y w67c23 strain (Lindsley and Zimm, 1992) was used for wild-type controls and generation of nos+1+3 transgenic lines. Deficiency stocks consisted of deficiency kits covering chromosomal arms 2L and 2R (Bloomington). The following mutants and transgenic lines were used: nosBN (Wang et al., 1994), aubQC42, aubHN2 (Schüpbach and Wieschaus, 1991), squHE47 (Pane et al., 2007), mnkp6 (Abdu et al., 2002), oskA87 (Jenny et al., 2006), nos-gal4-vp16; gfp-aub (Harris and Macdonald, 2001), FM7i GFP (Bloomington), hsp83-MCP-GFP (Forrest and Gavis, 2003), rump1 (Jain and Gavis, 2008). Unless otherwise indicated, aubQC/aubHN transheterozygotes were used as aub mutants and aubQC/+ as heterozygotes. For mnk, aub double mutants, mnkp6, aubQC42 and mnkp6, aubHN2 recombinant chromosomes were used in trans-heterozygous combination (Klattenhoff et al., 2007).
The nos+1+3 transgene includes the nos 5′UTR and coding region followed by the sensitized 3′UTR containing nucleotides 6-96 (the +1 element), 181-408 (the +3 element), and 548-786 of the nos 3′UTR (Gavis et al., 1996), inserted into pCaSpeR2. The transgene also contains MS2 stem-loops for in vivo mRNA visualization, inserted near the terminus of the 3′UTR; they do not affect the behavior of nos mRNA (Forrest and Gavis, 2003). Transgenic lines were generated by standard P element-mediated germline transformation (Spradling, 1986). Cloning details are available upon request.
Each deficiency stock from the second chromosome kits was crossed to generate Df/+; nosBN, nos+1+3/nosBN females from which embryos were collected overnight on apple juice plates. Embryonic cuticle preparation was performed as previously described (Crucs et al., 2000). The average number of segments and the standard error (SEM) were calculated using standard histogram distribution analysis (Graphpad Prism).
Embryos were collected from 0–2 hours after egg laying and in situ hybridization was performed as described (Gavis and Lehmann, 1992). Immunofluorescent staining of embryos aged 3–5 hours was performed as previously described (Duchow et al., 2005) using rabbit anti-Vas (1:10000; gift from R. Lehmann), Alexa Fluor-568 goat anti-rabbit (1:1000; Molecular Probes) and DAPI (1:1000). For the analysis of pole cell number, a z-series of each embryo, at 1.5 μm intervals from the first focal plane with a visible pole cell to the last, was taken with a Zeiss LSM510 confocal microscope and 40x/1.3 oil objective, and projections were generated using ImageJ (NIH).
Total RNA was extracted from dechorionated 0–1.5 hour old embryos using TRIzol reagent (Invitrogen) and northern blotting was carried out according to Bergsten and Gavis (1999). Quantitation of blots was performed by phosphorimaging (Molecular Dynamics).
Immunoblotting of extracts from 0–2 hour old embryos was performed as previously described (Forrest et al., 2004). Final antibody concentrations were: rabbit anti-Nos (1:1000; gift of A. Nakamura), rabbit anti-Osk (1:3000;Vanzo and Ephrussi, 2002), mouse anti-Snf (1:20000; gift of P. Schedl), and rabbit anti-Khc (1:30000; Cytoskeleton). Proteins were detected using the appropriate HRP conjugated secondary antibodies and Lumi-Light Western Blot Substrate (Roche). Quantitation was performed using an Alpha Innotech imager and AlphaEase software (Alpha Innotech) or using ImageJ (NIH).
RNA co-immunoprecipitation and RT-PCR analysis were performed as described (Jain and Gavis, 2008) except that extracts were prepared from freshly dissected ovaries and immunoprecipitation buffer contained 150 mM NaCl. RT-PCR analysis was performed with primers for nos (Jain and Gavis, 2008), osk (5′-AATGGATCCAGTGTGCAGAAAATC-3′ and 5′-AGCGAATGCTGTCACCTA-3′) and his3.3b (5′-GATTGATTCCGCATAAAGCGCG-3′ and 5′-AAGGAGCACGGCGCAACGTACA-3′). Protein co-immunoprecipitation using polyclonal anti-GFP antibody (Abcam 290) was performed according to Kalifa et al. (Kalifa et al., 2009) except that fresh ovaries were used and extracts were pre-incubated with Protein G Dynabeads (Invitrogen) for 1 hour at 4° C, then applied to anti-GFP-coated Protein G Dynabeads (Invitrogen) for 1 hour at 4° C. Samples were analyzed by SDS-PAGE and immunoblotting with monoclonal anti-GFP (Clontech JL-8) and anti-Rump (5G4) antibodies.
The nos localization signal is composed of four unique elements designated as +1, +2′, +3 and +4, no one of which is necessary or sufficient for wild-type nos mRNA localization (Gavis et al., 1996) (Fig. 1A). To sensitize nos mRNA to the loss of a candidate localization factor, we deleted the +2′ and +4 elements resulting in a transgene bearing only the +1 and +3 localization element sequences (nos+1+3; Fig. 1A). When this transgene is introduced into nosBN females, the transgenic nos+1+3 mRNA is the only maternal nos mRNA expressed. Because posterior localization of nos+1+3 mRNA is decreased relative to wild-type nos mRNA (Fig. 2A), embryos produced by these females exhibit reduced abdominal segmentation, forming an average of 6 of the 8 abdominal segments characteristic of wild-type embryos (Figs. 1A and B). For simplicity, we refer hereafter to this maternal genetic background as nos+1+3 and the resulting embryos as nos+1+3 embryos. To identify novel nos mRNA localization factors, we performed a deficiency screen of the second chromosome in the nos+1+3 background, reasoning that decreasing the dosage of a candidate localization factor would further compromise nos localization and, consequently, abdominal segmentation (Fig. 1A). A total of 18 of the 123 deficiencies tested produced a reduction of segment number to below a threshold of 3 abdominal segments (Table 1). These included deficiencies uncovering cappuccino (cap), chickadee (chic), staufen (stau), valois (vls) and vasa (vas), all of which have previously been implicated in patterning of the A-P axis (Hay et al., 1988; Lasko and Ashburner, 1988; Manseau and Schüpbach, 1989), validating the premise of the screen.
One deficiency that reduced abdominal segmentation to an average of 2.4 segments, Df(2L)BSC32 (Fig. 1B), is the subject of this report. Of the 78 genes contained within this deficiency, we focused on aubergine (aub), which had been previously identified in a screen for heterozygous suppressors of the bicaudal phenotype produced by misexpression of osk, and the consequent mislocalization of nos mRNA, at the anterior of the embryo. Although Osk protein is still produced at the anterior when osk is misexpressed in embryos heterozygous for aub mutations, nos mRNA is no longer ectopically localized. To explain the requirement for aub, it was proposed that Aub might regulate translation of factors acting downstream of Osk to mediate nos localization (Wilson et al., 1996). The identification of a deficiency uncovering aub by our screen suggests that aub could play a more direct role in nos mRNA localization. We therefore examined whether the reduction in abdominal segmentation observed in nos+1+3 embryos heterozygous for Df(2L)BSC32 is due to the elimination of aub. Maternal heterozygosity for a strong aub mutation (aubQC42/+; hereafter referred to as aub−/+) produced similar results to Df(2L)BSC32 while heterozygosity for a weaker aub allele (aubHN2/+) had an intermediate effect (Fig. 1B), suggesting that elimination of aub function results in the effect of Df(2L)BSC32 on abdominal segmentation.
More recently, Aub has been shown to be a member of the Piwi-related Argonaute family of proteins involved in the repeat-associated small interfering RNA (rasiRNA) pathway that silences retrotransposons in the germline (Kennerdell et al., 2002; Klattenhoff et al., 2007; Savitsky et al., 2006; Vagin et al., 2004). Aub interacts physically with Squash (Squ), a protein with nuclease homology that is involved in rasiRNA biogenesis (Pane et al., 2007). In contrast to aub, heterozygosity for a strong loss of function squ mutation does not reduce abdominal segmentation of nos+1+3 embryos (Fig. 1B). This result indicates that the observed decrease in nos+1+3 activity is specific to aub and not a general effect of mutations in rasiRNA pathway components.
To determine if the effect of aub on abdominal segmentation in the sensitized nos background is due to a defect in nos localization, we investigated the distribution of nos mRNA in aub−/+ embryos. Wild-type endogenous nos mRNA is localized to the posterior pole in these embryos, indistinguishably from wild-type embryos (Figs. 2A and B). However, localization of nos+1+3 mRNA, which is initially weaker than wild-type nos, is further decreased when nos+1+3 embryos are also aub−/+ (Figs. 2A and B), consistent with observed decrease in abdominal segmentation. Northern blot analysis confirmed that the total amount of nos+1+3 mRNA is comparable between the two genetic backgrounds (Fig. 2C). Additionally, localization of bcd mRNA to the anterior of the embryo is not disrupted, suggesting that reducing aub activity does not generally affect A-P patterning (Fig. 2D). Thus, these results suggest that aub plays a role in nos mRNA localization, possibly acting redundantly with other nos localization factors.
nos mRNA localization requires the prior localization and translation of osk at the posterior pole. In aub mutant ovaries, osk mRNA is prematurely translated, suggesting that Aub plays a role in osk mRNA silencing at early stages of oogenesis (Cook et al., 2004). Additionally, during mid-oogenesis, localization of osk mRNA and accumulation of Osk protein at the posterior of the oocyte is greatly diminished in aub mutant ovaries (Cook et al., 2004; Wilson et al., 1996). This effect is likely to be indirect, due to an earlier requirement for aub in the A-P polarization of the oocyte microtubule cytoskeleton that is in turn required for osk mRNA localization (Cook et al., 2004). However, because Osk levels are altered in aub mutants, we investigated whether the decreased localization of nos+1+3 mRNA in aub−/+ embryos could be also be due to an upstream defect in osk regulation. In aub−/+ embryos, osk localization appears wild-type (Fig. 3A) and these embryos express wild-type levels of osk mRNA and Osk protein (Figs. 2C and and3B).3B). Osk is a critical component of the germ plasm that is necessary to generate the germ cell precursors, or pole cells, at the posterior of the embryo (Ephrussi et al., 1991; Kim-Ha et al., 1991; Lehmann and Nusslein-Volhard, 1986). Pole cell formation is highly sensitive to osk and a decrease in Osk protein levels of as little as 15% results in a significant reduction in pole cell number (Riechmann et al., 2002). In aub−/+ embryos, the average number of pole cells is equivalent to the wild-type number (30.2 ± 6.7 versus 29.2 ± 5.0; Figs. 3C and D). Similarly, nos+1+3 and aub−/+; nos+1+3 embryos have comparable numbers of pole cells (33.0 ± 6.5 versus 29.8 ± 5.7; data not shown). Together, these results indicate that the loss of a single copy of aub affects nos mRNA localization without affecting osk activity.
aub mutants affect microtubule polarization and osk mRNA regulation by activating a DNA damage signaling pathway within the germline mediated by mnk and mei-41, the Drosophila homologs of Chk2 and ATR kinase respectively. Double mutants between aub and either mnk or mei-41 bypass the DNA damage response and suppress the effects of aub on osk translation leading to wild-type posterior accumulation of Osk protein (Klattenhoff et al., 2007). To address whether aub similarly affects nos mRNA localization by triggering the DNA damage response, we assessed Nos expression as a quantitative measure of nos mRNA localization in embryos from aub, mnk double mutant females. Embryos from aub mutant females express minimal Nos protein, consistent with their diminished Osk expression (Figs. 4A and B). While mutation of mnk alone has no effect on Nos or Osk levels, Osk expression is partially restored in aub, mnk double mutant females (Fig. 4A). By contrast, Nos protein remains largely undetectable in the aub, mnk double mutant extract (Fig. 4A).
To provide calibration for this assay, we determined the expected relationship between Osk and Nos levels by monitoring nos and osk mRNA localization and protein accumulation in embryos heterozygous for oskA87, an RNA null mutation (Jenny et al., 2006). In oskA87/+ embryos, osk mRNA is present at 60% of the wild-type level resulting in less osk localized at the posterior of the embryo (Supplemental Fig. 1). Consequently, Osk protein accumulates to approximately 50% of the wild-type level (Fig. 4D). The effect on osk is paralleled by a decrease in posteriorly localized nos (Supplemental Fig. 1), with Nos protein present at approximately 70% of wild-type levels (Fig. 4D). This response of Nos, which is largely correlated with the behavior of Osk, contrasts sharply with the complete failure of Nos to recover when Osk levels are partially restored in aub−, mnk− embryos. Together, these results demonstrate that aub affects Nos expression in a manner independent of the DNA damage response and its effect on osk localization. Moreover, they indicate that the nos localization defect in aub mutant embryos cannot be accounted for solely by the defect in osk localization, consistent with an osk-independent role for aub in nos localization.
To determine whether Aub might directly act as a nos localization factor, we performed co-immunoprecipitation experiments from ovarian extracts to test the interaction of Aub with nos mRNA in vivo. To facilitate Aub immunoprecipitation, we took advantage of a transgenic line expressing a functional GFP-Aub fusion protein (Harris and Macdonald, 2001). Following immunoprecipitation with anti-GFP antibody, RNA was isolated and analyzed by RT-PCR using primers for nos mRNA or for a control RNA (his3.3b). nos mRNA is detected in immunoprecipitates from GFP-Aub ovary extract but not from control extract of ovaries expressing GFP alone (Fig. 5A). Moreover, the control his3.3b RNA is not detected in either of the immunoprecipitates, indicating specificity of the interaction between Aub and nos. Because Aub is implicated in silencing of osk mRNA early in oogenesis (Cook et al., 2004), we also tested whether osk mRNA is co-immunoprecipitated with Aub. RT-PCR with primers for osk mRNA showed that this is indeed the case (Fig. 5A).
Co-immunoprecipitation of Aub with nos mRNA suggests that Aub may be part of a nos mRNA localization complex. To further test this hypothesis, we investigated whether Aub also interacts with Rump, the only known direct-acting nos localization factor (Jain and Gavis, 2008). GFP-Aub or a control RNA-binding protein, MCP-GFP, that does not bind to nos mRNA (Forrest and Gavis, 2003), was immunoprecipitated from ovary extracts using an anti-GFP antibody and the immunoprecipitates were analyzed by immunoblotting with an anti-Rump antibody. Rump is detected specifically in GFP-Aub immunoprecipitates, but co-immunoprecipitation with GFP-Aub is abolished if the extract is treated with RNase (Fig. 5B). This behavior indicates that Aub and Rump do not interact directly; rather, they may be incorporated into an RNP complex together via their interactions with the same target mRNA.
To determine whether aub and rump function together in nos regulation, we took advantage of a genetic assay previously used to characterize Rump as a nos localization factor (Jain and Gavis, 2008). Consistent with previous data (Jain and Gavis, 2008), embryos lacking rump exhibit a weak abdominal segmentation defect, with 10% developing fewer than 8 abdominal segments (Fig. 5C). Lowering nos mRNA levels by reducing the nos gene dosage to one copy raises the sensitivity to localization factor loss, increasing both the frequency and severity of abdominal segmentation defects. Comparable to previous results (Jain and Gavis, 2008), 31% of rump mutant embryos that are also heterozygous for nosBN develop with fewer than 8 segments (Fig. 5C). Heterozygosity for aub similarly exacerbates the segmentation defect of rump mutant embryos, resulting in 27% of embryos with fewer than 8 segments. Moreover, reducing both nos and aub gene dosage in rump mutant embryos leads to a further deficit, with 58% of embryos showing loss of abdominal segments (Fig. 5C). Together, these genetic and biochemical results, support a role for Aub as a component of a nos localization RNP complex.
Localization of nos mRNA to the posterior of the Drosophila embryo is critical for patterning of the A-P body axis. Although a cis-acting nos mRNA localization signal has been identified, the complement of trans-acting factors required for assembly of a nos RNP complex competent for posterior localization has remained elusive. From a sensitized genetic screen, we have identified Aub as a novel nos mRNA localization factor and show that Aub interacts with nos mRNA in vivo. Importantly, we show that nos localization is affected by aub acting downstream of osk mRNA localization, implying independent roles for aub in regulating these two transcripts. Although the role of aub in osk localization appears to be indirect, through a requirement in oocyte microtubule organization (Cook et al., 2004; Klattenhoff et al., 2007), our results suggest that aub plays a more direct role in regulating nos mRNA.
A decrease in aub activity leads to defects in nos mRNA localization and, consequently, in patterning of the A-P axis when nos localization signal redundancy is reduced by removing two localization elements. A similar behavior is observed in rump mutants, which exhibit only weak segmentation defects unless redundantly acting elements are removed from the nos localization signal (Jain and Gavis, 2008). Presumably, elimination of individual localization signal elements compromises localization by stripping away the contributions of nos localization factors with overlapping functions in nos RNP assembly. Conversely, elimination of multiple nos localization factors should lead to a more severe defect than elimination of an individual factor. Consistent with this prediction, decreasing aub gene dosage in rump mutants also leads to more severe loss of abdominal segments.
In addition to allowing us to uncover a requirement for aub, the sensitized nos+1+3 background has allowed us to separate the indirect requirement for aub in osk localization from a more direct requirement in nos localization. Defects in osk regulation and abdominal segmentation are only observed when females are homozygous mutant for aub and not when they are heterozygous. By contrast, defects in nos+1+3 localization are observed when females are heterozygotes for aub mutations. Our results are further supported by previous data showing that the ability of ectopically expressed Osk to recruit nos mRNA is compromised in aub−/+ embryos (Wilson et al., 1996).
Aub has been implicated in the rasiRNA pathway that silences retrotransposons in the germline (Kennerdell et al., 2002; Klattenhoff et al., 2007; Savitsky et al., 2006; Vagin et al., 2004). However, mutation of squ, which encodes a rasiRNA pathway component that interacts with Aub (Pane et al., 2007), has no effect on the nos+1+3 transgene. Interestingly, another rasiRNA pathway component, piwi (Cook et al., 2004), has the opposite effect of aub on the nos+1+3 transgene, as heterozygosity for a piwi mutation results in increased segmentation in the sensitized background (data not shown). Mutations that inactivate the rasiRNA pathway, including aub mutations, activate the DNA damage checkpoint, presumably due to unsuppressed transposon activity (Chen et al., 2007; Klattenhoff et al., 2007). Checkpoint activation disrupts microtubule organization and grk translation, resulting in a failure of axis specification that is thought to lead to subsequent defects in osk mRNA localization (Klattenhoff et al., 2007). However, the effect of aub mutation on nos+1+3 mRNA localization is independent of the DNA damage pathway, providing further evidence that Aub regulates nos independently of osk. Moreover, these results indicate that Aub function in nos localization is distinct from its function in RNA silencing.
Biochemical experiments indicate nos mRNA forms a complex with Aub in vivo, although whether Aub interacts directly with nos mRNA, or is recruited to the complex by other proteins that bind directly to nos, is not yet clear. We have been unable to obtain soluble recombinant Aub necessary to distinguish between these possibilities. However, the RNA-dependent co-purification of Aub and Rump, combined with evidence for genetic interactions between aub and rump further supports the contribution of Aub to the formation and/or function of a nos localization RNP complex. Whereas Rump is not concentrated at the posterior of the oocyte, Aub-GFP is localized to the posterior during midoogenesis and continues to accumulate at the posterior pole throughout the later stages of oogenesis when nos becomes localized (Harris and Macdonald, 2001)(data not shown). Thus, the contributions of Rump and Aub to nos RNP complexes may be dynamic, with both proteins accompanying nos as it is dispersed throughout the oocyte during ooplasmic streaming, but only Aub remaining associated with the nos RNP upon its entrapment at the posterior. Isolation and characterization of the full complement of nos localization factors will be essential to dissect the assembly pathway for nos localization complexes. The isolation of aub in a sensitized genetic screen validates the use of such an approach, in addition to biochemical purification strategies that proved successful for isolation of Rump, for achieving this goal.
(A) Northern blot of total mRNA isolated from either wild-type or oskA87/+ embryos, probed simultaneously for nos and for rp49 as a loading control. The blot was then stripped and reprobed for osk. Relative nos and osk mRNA levels, after normalization to rp49, are indicated below each sample set. (D) In situ hybridization to nos and osk in embryos from wild-type or oskA87/+ females.
We thank A. Pane, T. Schüpbach, and P. Macdonald for fly stocks and A. Nakamura, A. Ephrussi, R. Lehmann, and P. Schedl for antibodies. We also thank J. Goodhouse for assistance with confocal microscopy and S. Chatterjee for technical assistance. This work was supported by a grant from the National Institutes of Health (GM067758) to E.R.G. and by an NSERC postgraduate fellowship (A.N.B.).
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