Search tips
Search criteria 


Logo of plosonePLoS OneView this ArticleSubmit to PLoSGet E-mail AlertsContact UsPublic Library of Science (PLoS)
PLoS One. 2010; 5(11): e13827.
Published online 2010 November 3. doi:  10.1371/journal.pone.0013827
PMCID: PMC2972218

Mice Lacking Alkbh1 Display Sex-Ratio Distortion and Unilateral Eye Defects

Joseph Najbauer, Editor



Eschericia coli AlkB is a 2-oxoglutarate- and iron-dependent dioxygenase that reverses alkylated DNA damage by oxidative demethylation. Mouse AlkB homolog 1 (Alkbh1) is one of eight members of the newly discovered family of mammalian dioxygenases.

Methods and Findings

In the present study we show non-Mendelian inheritance of the Alkbh1 targeted allele in mice. Both Alkbh1−/− and heterozygous Alkbh1+/− offspring are born at a greatly reduced frequency. Additionally, the sex-ratio is considerably skewed against female offspring, with one female born for every three to four males. Most mechanisms that cause segregation distortion, act in the male gametes and affect male fertility. The skewing of the sexes appears to be of paternal origin, and might be set in the pachythene stage of meiosis during spermatogenesis, in which Alkbh1 is upregulated more than 10-fold. In testes, apoptotic spermatids were revealed in 5–10% of the tubules in Alkbh1−/− adults. The deficiency of Alkbh1 also causes misexpression of Bmp2, 4 and 7 at E11.5 during embryonic development. This is consistent with the incompletely penetrant phenotypes observed, particularly recurrent unilateral eye defects and craniofacial malformations.


Genetic and phenotypic assessment suggests that Alkbh1 mediates gene regulation in spermatogenesis, and that Alkbh1 is essential for normal sex-ratio distribution and embryonic development in mice.


The Eschericia coli (E. coli) DNA repair enzyme AlkB demethylates e.g. 1-methyladenine (1-meA) to adenine – generating succinate and formaldehyde – in the presence of iron as cofactor and 2-oxoglutarate as cosubstrate [1], [2]. To date, eight AlkB homologs have been identified in the mammalian genome [3]. Except for Alkbh5, all the remaining proteins have been identified throughout the animal kingdom, suggesting fundamental roles in biological processes [4]. Two of these homologs, ALKBH2 and ALKBH3 in humans (Alkbh2 and Alkbh3 in mice), are similar to E. coli AlkB in that they efficiently repair damaged nucleic acids in the presence of iron and 2-oxoglutarate in vitro [5][9]. In mice, Alkbh2 is the major, probably only, dioxygenase that repairs 1-meA DNA in vivo and mice lacking Alkbh2 accumulate 1-meA in the genome during ageing [10]. This year, two groups reported that Alkbh8 is a tRNA methyltransferase required for the final step in the biogenesis of mcm5U [11], [12]. ALKBH8 plays important roles in the survival and progression of human bladder cancer both in vitro and in vivo [13]. A likely ninth AlkB homolog, the obesity-associated Fto protein, was shown to have potential to demethylate 3-methylthymine (3-meT) [14], [15]. Crystal structure of the FTO protein recently confirmed this, and indicated that single-stranded RNA is the primary substrate of FTO [16]. Similarly, recombinant truncated Alkbh1 enzyme may demethylate 3-methylcytosine in vitro [17], but it remains unclear whether this activity is physiologically relevant.

All eight mammalian AlkB homologs contain the conserved iron- and 2-oxoglutarate dioxygenase domain. However, the region of E. coli AlkB that interacts with the nucleic acid substrate, the N-terminal nucleotide recognition lid, does not share sequence similarity with the mammalian homologs. Therefore, one cannot exclude the possibility that the targets of such proteins are not nucleic acids, but other macromolecules such as proteins. Since JmjC histone demethylases remove methyl groups from histones using the same mechanism as E. coli AlkB, it has been suggested that Alkbh1, 4 and 7 might be involved in histone/protein demethylation [18], [19]. However, for Alkbh1 we, and others, have been unable to identify DNA/histone demethylation activity [6], [7], [20], [21]. In 2008 a paper on Alkbh1 was published by Pan et al, where a gene-targeting study in mice showed that Alkbh1 localizes to nuclear euchromatin and functions in epigenetic regulation of gene expression [20]. Their study demonstrated impaired placental trophoblast lineage differentiation in Alkbh1−/− mice, and a strong interaction of Alkbh1 with Mrj, an essential placental gene that mediates gene repression by recruitment of class II histone deacetylases (HDAC) [20].

In the present study we attempt to elucidate the role of Alkbh1 by targeted deletion in C57/BL6 mice. We demonstrate that Alkbh1 deficiency in mice results in apoptosis in adult testes and sex-ratio distortion of offspring, most likely caused by defects in the pachytene stage during spermatogenesis. An incompletely penetrant phenotype apparent during embryonic development is consistent with Bmp2, 4 and 7 misexpression. Although many mechanistic aspects of Alkbh1 function remain to be revealed, these results show that Alkbh1 is crucial for normal embryonic development and viability in mice, and plays an important role during spermatogenesis.

Materials and Methods

Generation of Alkbh1 Targeted Mice

A specific 360-bp murine probe of exon 6 in the Alkbh1 gene was amplified from mouse genomic DNA by polymerase chain reaction (PCR) and used to screen a 129 SvJ mouse genomic library (Stratagene). To generate the targeting construct, we subcloned fragments from a ~14-kb genomic clone on both sides of neomycin (neo) in the pGT-N38 vector (New England Biolabs). Homologous arms consisting of a 3.0-kb MfeI/HindIII fragment and a 3.7-kb BsrGI fragment facilitated removal of a 3.8-kb HindIII/BsrGI fragment including exon 6 and replacement with the neo cassette. The targeting construct was electroporated into 129 SvJ embryonic stem (ES) cells, and transfectants were selected in geneticin (G418) and expanded for further analysis. Chimaeric mice were produced by microinjection of one targeted ES cell clone with normal karyotype into C57/BL6 blastocysts at embryonic day 3.5 (E3.5). We verified germline transmission of the targeted allele by Southern-blot analysis of ScaI-digested genomic DNA on the 5′ end and PCR analysis on the 3′ end. 5′ and 3′ homologous recombination in the F1 generation were confirmed by PCR analysis. Heterozygous males were backcrossed for three generations onto C57/BL6 females. All mouse experiments were approved by the Norwegian Animal Research Authority (Ref. nr. 08/9940) and done in accordance with institutional guidelines at the Centre for Comparative Medicine at Oslo University Hospital. Animal work was conducted in accordance with the rules and regulations of the Federation of European Laboratory Animal Science Association's (FELASA).


For Alkbh1 genotyping, ear-clip samples were degraded by incubation in PBND buffer (50 mM KCl, 10 mM Tris-HCl pH 8.3, 2.5 mM MgCl2-6H2O, 0.1 mg/ml gelatin, 0.45% v/v NP40, 0.45% v/v Tween 20) and 0.5 mg/ml proteinase K at 55°C over night. Samples were heated to 95°C for 10 min to inactivate proteinase K, and PCR amplified for 35 cycles with an annealing temperature of 60°C (see primers below). For sex genotyping of embryos, a small piece of tissue was obtained from the embryosac or -tail and washed three times in PBS to eliminate maternal contamination. The tissue was degraded by a 3-hour incubation, and subsequently treated as above. PCR analysis of Sry (Y-linked gene) was performed to determine maleness and Rapsn was used as an autosomal, internal control as described (Mouse Phenotypes, a Handbook of Mutatation Analysis, Cold Spring Harbor laboratory press, Chapter 3, page 40, 2005).

Primers wild-type allele (WT): 5′-AGTTATCAGGGCCATCCAGGGAGGT-3′


Primers targeted allele (KO): 5′-GCTTGCCGAATATCATGGTG-3′


Whole-Mount In Situ Hybridization

We carried out whole-mount in situ hybridization on E9.5 to E12.5 embryos fixed in paraformaldehyde as described (Henrique et al. 1995). Mouse antisense and sense (control) RNA probes were prepared using DIG RNA labeling mix (Roche) together with T3 or Sp6 and T7 RNA polymerases (Roche). Templates for the labeling reaction were PCR products amplified from full-length mouse cDNA with T3, Sp6 or T7 promoters added to the PCR primers. For Alkbh1 the template contained 465-bp of exon 6, for Bmp2 519-bp of exon 2–3 and for Bmp7 559-bp of exon 2–5. For Bmp4, linearized pSP72 plasmid with a 1550-bp insert was used as template. Embryos were examined on a SMZ1500 microscope (Nikon).

Quantitative Real-Time PCR (qPCR) Analysis

Total RNA was isolated from embryos, organs and germ cells using the Fast RNA Pro Green Kit (MP Biomedicals) according to the manufacturers protocol. Any DNA remnants were removed using TURBO DNase (Ambion) and cDNA was made using High Capacity cDNA Reverse Transcription Kit (Applied Biosystems). The quantitative PCR reactions were carried out on a StepOnePlus or 7500 Fast instrument using 50 ng cDNA, TaqMan® Fast Universal PCR Master Mix and appropriate TaqMan primers and probes (all from Applied Biosystems). Pre-designed primers and probes were used both for the target genes (Alkbh1, Vav2, Mapk8, Ccdc80, Rest, and Hif1a) and endogenous controls (Gapdh, 18s and β-actin). All samples were run in triplicates and with one technical parallel (2 runs per sample). The relative quantity was calculated using the equation RQ = 2−ΔΔCT, where RQ is the relative quantity of the target gene. ΔΔCT is the difference in CT-value between the target gene and the endogenous control minus the difference in CT-values between the reference gene and the endogenous control.

STAPUT Isolation of Testicular Cells

Male germ cells were isolated from testes using an adapted version of the STAPUT method [22]. Pachytene cells and round spermatids were isolated from six 12-week old males, while a total of sixty 10-day old males were sacrificed for the isolation of type A and type B spermatogonia. The testes were put in ice cold DMEM medium containing antibiotics and then carefully detunicated. The tubules were treated with DNaseΙ, collagenase, trypsin and hyaluronidase (all from Sigma-Aldrich) at 34°C to remove connective tissue and somatic cells, yielding a cell suspension of germinal cells in DMEM containing 0.5% BSA. The cell suspension was loaded into the cell loading chamber of the STAPUT apparatus and separated by sedimentation velocity at unit gravity in a 2–4% w/v BSA gradient in DMEM medium at 4°C for 2.5 hours. After sedimentation, 10 ml fractions were collected and checked under the microscope. Fractions containing pure germ cells were pooled and the cell number counted in a Countess® Automated Cell Counter (Invitrogen). Cells were spun down and the pellet was snap frozen in liquid nitrogen before placed in −70°C. An aliquot of isolated cells was fixed on SuperFrost Plus slides (VWR) using Cell Adherence Solution (Crystalgen, Lot no 425081) for microscopic analysis of purity.

TUNEL Assay of Testes

We fixed testes from 3- and 9-month old animals in neutral-buffered formalin, progressively dehydrated them in a graded ethanol series, and embedded them in paraffin. Sections (4-µm) were deparaffinized and treated with proteinase K for 15 min and quenched in 3% hydrogen peroxide in PBS for 5 min at room temperature. Subsequently, nuclear staining in apoptotic cells was detected using ApopTag kit (Chemicon, according to the manufacturers instruction. Sections were analysed on an Axioplan 2 microscope (Zeiss).

Immunofluorescent Staining of Testicular Cells

Testicular cells from 12-month old males were spread on SuperFrost Plus slides (VWR), progressively dehydrated in a graded ethanol series and dried completely. Slides were washed in 1× PBS and fixated in 4% PFA in PBS. Slides were blocked in 5% serum in PBS for 1 hour at room temperature and incubated with primary antibodies overnight at 4°C prior to detection with secondary antibodies. Primary antibodies used were rabbit anti-MacroH2A (1[ratio]500, Upstate) and mouse anti-FK2 (1[ratio]5000, Biomol). Secondary antibodies used were goat anti-rabbit Alexa Fluor 488 (green dye) (Invitrogen) and goat anti-mouse Alexa Fluor 594 (red dye) (Invitrogen), respectively. Single Z-sections were captured by Axioplan 2 microscope (Zeiss).

DNA Microarray Analysis

High quality of total RNA extracted from adult testes was verified on Agilent Bioanalyzer 2100 (RIN value between 9.8 and 10.0). 15 µg of biotinylated and fragmented cRNA was then hybridized onto the GeneChip Mouse Genome 430 2.0 Array (Affymetrix) according to manufacturers protocols (Affymetrix). QCs including scale factor, background, noise, spikes and RNA degradation were checked and validated using the yaqcaffy library (

Affymetrix raw data was generated with GCOS 1.4 (GeneChip Operating Software, Affymetrix), and the signal intensities of each probe set were normalized with the RMA (Robust Microarray Anlaysis) algorithm. To find differentially expressed genes, t-test with randomized variance was used as statistical test and the cut-off (p-value) was set to 0.05 with a FDR correction. Class comparison analysis was used to identify interesting genes. The signal in one group was always (i.e. for all the triplicate) higher or lower compared to the other group. Fold change for all the genes that passed the above criteria was computed and only the genes with ≥2-fold change were studied. The heatmap was generated using the GeneSpring GX 10 demoversion (Agilent). All data is MIAME compliant and the raw data has been deposited in a MIAME compliant database, the accession number is GSE22073.

Skeletal Staining

For skeletal analysis, skin and internal viscera of E18.5 embryos and newborn mice were removed. We then fixed the animals overnight in 95% ethanol and carried out Alcian blue 8GX (Sigma) and Alizarin red S (Sigma) staining of cartilage and bone, respectively, as described (Manipulating the Mouse Embryo, 3rd edition, Cold Spring Harbor laboratory press, Chapter 16, Protocol 22, pages 699–700, 2003). The skeletons were photographed with a Nikon D80 camera.

Histological Analysis of Eyes

We fixed adult eyes in neutral-buffered formalin or paraformaldehyde added 20% absolute alcohol for 24 hours, progressively dehydrated them in a graded ethanol series, and embedded them in paraffin. Sections (4-µm) were deparaffinized, rehydrated and stained with hematoxylin and eosin. Sections were analysed on an AxioCam HRc microscope (Zeiss).


Deletion of Alkbh1 in Embryonic Stem Cells and Mice

To gain more insight into the role of the Alkbh1 dioxygenase we have generated mice lacking Alkbh1. Alkbh1 was the first mammalian AlkB homolog to be identified [23], and is the AlkB homolog most similar in sequence to Eschericia coli (E. coli) AlkB. The region of greatest similarity includes 107 amino acids, 37% of which are identical between the E. coli and mouse Alkbh1. The conserved RvNmTvR and HvD…H motifs of the 2-oxoglutarate and iron binding sites, respectively, are also present in both proteins. The conserved domains of Alkbh1 are encoded by exon 5 and 6 at the 3′ end of the mouse Alkbh1 gene. To fully eliminate the activity of Alkbh1 and keep the overlapping Nrp gene intact, we substituted exon 6 with a neomycin-resistance gene cassette by homologous recombination in mouse embryonic stem cells (Figs. 1A–D). The expression of the Nrp gene was confirmed by qPCR (data not shown).

Figure 1
Targeted disruption of Alkbh1 in embryonic stem cells and mice.

Expression Analysis of Alkbh1 in Embryos, Organs and Male Germ Cells

The expression pattern of Alkbh1 was analysed in embryos at different stages by whole-mount in situ hybridization (Fig. 2A) and by qPCR (Fig. 2B). Weak expression of Alkbh1 was observed throughout the embryo at E8.5 (data not shown). As the cells migrate and differentiate during organogenesis the expression becomes more specific, and Alkbh1 was detected in the spinal cord, forebrain and branchial arches at E9.5, and also in limb buds at E10.5 (Fig. 2A). Peak expression was detected at E11.5 in the frontonasal process including telencephalon (tc), maxillary, mandibular and hyoid arches (ba), upper and lower limb buds (lb), and midbrain and rhombomere 1 (r1) roof plates (rp) (Fig. 2A). Alkbh1 expression decreased considerably from E11.5 to E12.5 (Fig. 2A–B). In adult organs, Alkbh1 was highly expressed in testis (RQ = 44.0), with slightly lower expression in eye, brain and kidney (RQ = 16.0, 15.4, 14.4) (Fig. 2C). Moreover, the expression of Alkbh1 was studied at different stages during spermatogenesis, and was found to be significantly elevated in the pachytene spermatocytes (PS) (RQ = 11.3) compared with spermatogonia A and B (Sg A, Sg B) and round spermatids (RSd) (RQ = 1.7) (Fig. 2D). This is the third stage of the prophase of meiosis I, in which synapsis is completed and homologous recombination occurs. Thus, Alkbh1 may have considerable potential for gene-function in embryonic development and in the pachytene stage during spermatogenesis.

Figure 2
Expression of Alkbh1 in embryos, organs and male germ cells.

Non-Mendelian Inheritance and Sex-Ratio Distortion in Alkbh1 Targeted Mice

Mendelian inheritance, in which each parent contributes one of two possible alleles for a given trait, has a characteristic ratio of 1[ratio]2[ratio]1 after heterozygous crosses. Initial crosses of mice carrying either one or two targeted Alkbh1 loci revealed non-Mendelian distribution. Therefore, we carried out extensive breeding analysis and genotyped more than 1400 Alkbh1 mutant mice and embryos (Fig. 3). Following heterozygous breedings, the survival of Alkbh1−/− pups after 1 month was only 20% compared with wild-type littermates (Fig. 3A). In addition, the frequency of viable Alkbh1+/− mice was only 60% of the expected rate (Fig. 3A). The non-Mendelian distribution was clearly significant with a p-value of 3.8×10−72-test). A similar pattern was observed in Alkbh1+/− male x Alkbh1−/− female crosses, p = 5×10−42-test) and Alkbh1−/− male x Alkbh1+/− female crosses, p = 3.7×10−52-test) (Fig. 3C). In general, the average litter size decreased as the number of targeted alleles in the parental generation increased (Fig. 3B). The mean litter size was 9.2 for wild-type crosses, 6.2 for heterozygous crosses and 3.2 for homozygous crosses (Fig. 3B). Notably, paternal inheritance of the targeted allele seemed to be more critical than maternal transmission for the survival of offspring. Another evident phenotype was the growth retardation observed in viable Alkbh1−/− mice compared with wild-type littermates (Fig. S1).

Figure 3
Non-Mendelian inheritance and sex-ratio distortion in Alkbh1 targeted mice.

One process of non-Mendelian inheritance is segregation distortion. There are a number of mechanisms that can cause segregation distortion, and both autosomal sex-ratio distortion as well as segregation distortion of the sex chromosomes exist [24]. In Alkbh1+/− male x Alkbh1−/− female crosses, the ratio of female to male homozygous offspring at 1 month was approximately 1[ratio]1 (Fig. 3C, left panel). In Alkbh1−/− male x Alkbh1+/− female crosses, the ratio of homozygous Alkbh1−/− pups was significantly skewed against females, with one female born for every three to four males (Fig. 3C, right panel). The survival of Alkbh1−/− male pups was 60% compared with Alkbh1+/− pups, whereas the proportion of viable Alkbh1−/− female pups was only 18%, p = 7.1×10−52-test) (Fig. 3C, right panel). Following heterozygous crosses, the survival of Alkbh1−/− offspring was significantly reduced, 30% of the males and just 10% of the females survived compared with wild-type littermates, p = 1.4×10−62-test) (data not shown). A sex-ratio distortion was also seen in mid-stage Alkbh1−/− embryos (E10–E12.5) after heterozygous breedings (17 litters), with 89% male and 60% female embryos present compared with wild-type embryos (data not shown).

Spermatogenic Defects in Alkbh1 Deficient Testis

Reduced testis weight was observed in Alkbh1−/− males at 12-week and 12-month of age, constituting three-quarters and two-thirds the mean weight of testis from wild-type littermates, respectively (Fig. 4A). TUNEL staining of testes from 12-week old wild-type and Alkbh1−/− males were histologically indistinguishable and showed no apoptotic cells (data not shown). On the other hand, extensive apoptosis and reduced number of germ cells were revealed in 5–10% of the seminiferous tubules in 9-month old Alkbh1−/− males (Fig. 4B, Fig. S2). In Alkbh1−/− testes, no apoptosis was detected in the spermatogonia (Sg) located at the edges of the tubules and in the meiotic spermatocytes (Sc) residing mostly in the two to three subbasal layers (Fig. 4B, Fig. S2). However, numerous apoptotic and degraded cells were seen in the subbasal regions corresponding to spermatocytes and spermatids, as well as in degenerating round and elongating spermatids (Sd) in the more luminal layers of the tubules (Fig. 4B, Fig. S2). In wild-type, a few apoptotic cells were occasionally located mainly at the basal layer of the seminiferous tubules (Fig. 4B, Fig. S2). To better define the basis for arrest in germ cells and the sex-ratio distortion, we focused on the XY-body in the pachytene stage of meiosis. The XY-body is a condensed chromatin structure containing the sex chromosomes, which is thought to be essential for meiotic progression. In mid-pachynema the XY-body forms a spherical structure near the nuclear periphery [25]. Two different markers against XY-bodies were used, macroH2A and FK2, however visible sex-bodies were readily identified in pachytene spermatocytes from 12-month old wild-type and Alkbh1−/− testes (Fig. 4C). MacroH2A recognizes the sex chromatin, and FK2 detects the abundant ubiquitination of H2A in the XY-body. We also did antibody staining against several specific stages throughout spermatogenesis, but no significant differences between wild-type and Alkbh1−/− mice were revealed (Fig. S3). The fact that sex-body formation is not impaired in Alkbh1-null males does not exclude the hypothesis of an epigenetic and silencing defect of the paternal X chromosome in those mice. Another possibility is that the skewing of the sexes in Alkbh1−/− mice is related to autosomal sex-ratio distortion. It is well known that most mechanisms that affect segregation distortion act in the male gametes and affect male fertility [24].

Figure 4
Spermatogenic defects in Alkbh1 deficient testis.

Expression Profiling in Wild-Type and Alkbh1−/− Testis

Due to the pivotal role of Alkbh1 in mouse survival and potentially in germ cells, we searched for Alkbh1-regulated genes in adult testes. Microarray analysis of whole testes from 12-week old males identified 25 genes that were differentially expressed in Alkbh1−/− versus wild-type, using the class comparison strategy (Fig. 5A). Ptpro were also statistically significantly upregulated in Alkbh1−/− testes (Table S1; All data is deposited in GEO, accession number GSE22073). The function of PTPRO in adult testis has not been explored, but Avraham et al found expression of PTPRO in testis in humans [26]. Ptpro is suggested to be involved in the differentiation and axonogenesis of central and peripheral nervous system neurons, where it is in position to regulate phosphotyrosine levels in intracellular signaling cascades [27]. qPCR was performed on selected genes, to verify the class comparison analysis (Fig. 5B). Upregulation of Vav2 and Ccdc80 was confirmed in Alkbh1−/− versus wild-type whole testes. Vav2 is a guanine nucleotide exchange factor important for the formatin of adherens junctions between Sertoli cells and spermatids in testis, as well as in the formation of synapses in neurons [28]. The function of Ccdc80, also known as steroid sensitive gene 1, has not been studied in testis, but is supposed to be expressed in this organ according to its EST profile in the Unigene database ( Ccdc80 is expressed in human mesenchymal stem cells and mouse embryo cartilage, suggesting a role in skeletogenesis [29]. Together, these findings point towards a role in regulating the expression of genes having diverse functions – in spermatogenesis, in the nervous system and in skeletogenesis, although the genes affected in the microarray analysis are merely indirect targets of the Alkbh1 protein.

Figure 5
Expression profiling in wild-type and Alkbh1−/− adult testis.

Alkbh1 Deficiency Causes Unilateral Eye Development

The reduced viability of Alkbh1 deficient mice and the expression pattern of Alkbh1 during embryonic development prompted us to analyse embryos and mice at earlier developmental stages. Both Alkbh1+/− and Alkbh1−/− mice showed embryonic (E) and postnatal (P) lethality, ranging from E9.5 to P28 (data not shown). Both embryos and neonatal mice clearly displayed an incompletely penetrant defect of small (microphthalmia) or missing (anophthalmia) eyes, and most often in the right eye (unilateral) (Fig. 6A, D). Eye malformations such as microphthalmia and anophthalmia occur in the mouse if eye morphogenesis is disrupted during the critical stages between E9.5 and E13.5 [30]. Small or missing eyes were observed in 18% of Alkbh1−/− embryos (n = 7/39) and 9% of Alkbh1+/− embryos (n = 7/79) at E11.5–E12.5. In surviving adults, eye defects were observed in 9% of Alkbh1−/− mice (n = 14/150) and 0.5% of Alkbh1+/− mice (n = 1/198). Eye defects varied from unilateral (one side) to bilateral (both sides) microphthalmia or anophthalmia, or unilateral microphthalmia in combination with unilateral anophthalmia (Fig. 6A, D). Intriguingly, the disturbed eye development affected the right eye more severely than the left eye, bearing resemblance to the histone arginine demethylase Jmjd6 and the HMG box factor Sox3 null phenotypes in mice [31][33].

Figure 6
Eye and skeletal phenotype of Alkbh1−/− embryos and newborns, showing ossified areas in red and cartilage in blue.

To identify any abnormalities in addition to small or missing eyes, E18.5 embryos and newborn mice were analysed by skeletal staining of bone (Alizarin red) and cartilage (Alcian blue). Multiple defects were detected in the craniofacial, sternum and limb skeleton of mice lacking Alkbh1 (Figs. 6A–F). In the skull, reduced or missing intramembranous ossification resulted in enlarged sutures (Figs. 6B–C, F), while in the sternum, delayed ossification and aberrant fusion of the sternal bands were observed (Fig. 6E). Skeletal staining also showed assymetric shortening of the nasal bones, curving unilaterally in Alkbh1−/− mice causing mal-developed teeth (Fig. S4A), as well as reduced ossification in the phalanges (P) and the metatarsals (M) of the autopod of Alkbh1−/− newborns (Fig. S4B). The most crucial step in skeletal morphogenesis is the formation of mesenchymal condensations at E9.5 to E11.5 in mouse development [34]. The Alkbh1 variable phenotype indicates incomplete condensation of mesenchymal cells during skeletogenesis.

Incomplete Penetrance of Unilateral Eye Defects

Penetrance is described as incomplete when a trait associated with a specific allele is expressed in a proportion of the population carrying the allele variant [35]. The eye phenotype associated with lack of the Alkbh1 allele is characterized by incomplete penetrance (Fig. 7A–B). The Alkbh1−/− mouse in Fig. 7B has developed normally except for the deficiency of one eye. In contrast, the Alkbh1−/− embryo in Fig. 7A has gross developmental abnormalities, in addition to one small eye with only a residual mass of retinal cells, and one eye missing. The excessive brain tissue outside the skull is characteristic of a condition in which the neural tube fails to close, called exencephaly. Exencephaly is a neural tube defect (NTD), together with spina bifida (open spine) and anencephaly (open skull) [36]. At E10.5–E11.5, NTDs were observed in 23% of Alkbh1+/− embryos (n = 12/52) and 10% of Alkbh1−/− embryos (n = 3/31). The defects originated primarily from disrupted closure in the midbrain-hindbrain region (Fig. 7A) and upper spinal region, and were frequently associated with head and facial malformations (Fig. S4C). Around 50% of embryos with NTDs simultaneously displayed eye malformations (n = 14/27). The eye- and NTD-defects observed in Alkbh1 mutants correspond with the expression pattern of Alkbh1 seen in embryos and adult mice.

Figure 7
Incomplete penetrance of eye defects and exencephaly of Alkbh1−/− embryos and adults.

Gross morphological and histological analysis of adult Alkbh1−/− eyes revealed a range of serious deformities and size variations (Fig. 7C–D). Hematoxylin and eosin (HE) staining of paraffin-embedded sections showed that the lens was either completely missing or clearly smaller and displaced in the eye field (Fig. 7D). Furthermore, the lens fiber cells had lost their ordered lamination pattern, and swollen and liquefied fibers as well as vacuoles were seen throughout the lens (Fig. S4D). In retinal cells, there was a severe loss of organization even though all the retinal cells were present (Fig. 7D). In some areas, the neural retina (NR) was dysplastic with inclusions of rods and cones surrounded by outer nuclear layer cells (ONL), forming rosettes (Fig. 7E). In others, regions of thick layers of retinal pigment epithelium (RPE) cells were observed, with RPE cells appearing inside the NR layers in direct contact with the lens (Fig. 7E). Hence, Alkbh1 is important for growth and appropriate positioning and survival of lens and retinal cells.

Altered Expression of Bmps in Alkbh1 Deficient Embryos

Embryonic development and tissue regeneration are regulated by four major families of signaling molecules. One of the largest families is the bone morphogenetic proteins (Bmps) [37]. In skeletogenesis, Bmp signaling plays an important role in regulating chondrocyte differentiation and establishment of joint boundaries [38]. Current evidence indicates that Bmp2, Bmp4 and Bmp7 are the main source of Bmp signaling in vertebrate limb buds [39]. Similar signaling mechanisms are suggested for growth and regional specification of the forebrain, branchial arches and eye during development [40][42]. This prompted us to examine the expression of Bmp2, Bmp4 and Bmp7 in apparently normal Alkbh1−/− embryos at E11.5 (Fig. 8A). Bmp2 and Bmp7 were induced in the lateral telencephalon (tc) of Alkbh1−/− embryos, and expression of Bmp2 also increased in the frontonasal process (Fig. 8A). Moreover, Bmp4 and Bmp7 became upregulated specifically in the maxillary and mandibular cleft, while Bmp2 was upregulated throughout the maxillary, mandibular and hyoid mesenchyme (Fig. 8A). In limb buds, Bmp4 and Bmp7 were highly upregulated in the apical ectodermal ridge (AER) and in two broader domains anteriorly and posteriorly (Fig. 8B). Bmp2 expression disappeared from the posterior domain in hindlimb, and expression in AER of forelimb diffused proximally into the mesenchyme (lm) (Fig. 8B). The disrupted expression of Bmp2, Bmp4 and Bmp7 might be the cause of the somewhat smaller limb buds in Alkbh1−/− embryos. Regulation of these Bmp genes is important for AER formation, which is the major signaling center for limb outgrowth [37]. In general, both increased and decreased Bmp signaling can result in skeletal phenotypes [38].

Figure 8
Misexpression of Bmp2, Bmp4 and Bmp7 in Alkbh1 deleted embryos at E11.5.


Our data point towards an important role of Alkbh1 in spermatogenesis and embryonic development. Several genes involved in spermatogenesis, in the nervous system and in skeletogenesis were found to be differentially expressed in Alkbh1−/− whole testes. Adult males deficient in Alkbh1 exhibited dramatically increased levels of apoptosis in 5–10% of the seminiferous tubules of testes; in spermatids and in degenerated germ cells in the subbasal regions corresponding to spermatocytes and spermatids. The reduced number of all spermatogenic cells in the apoptotic tubules, might reflect an indirect effect of prolonged arrest in spermatids in the affected tubules. Similar nonspecific defects have been seen in miwi-null mice [43] and TRF2 mutants [44], [45]. Most genes involved in spermatogenesis display pleiotropic and leaky mutant phenotypes, as presented in this paper. Targeted disruptions of genes resulting in a variable range of defects and incomplete penetrance of spermatogenesis is even the case for regulatory genes, such as those encoding RNA binding proteins DAZLA [46] and MVH [47], and cell cycle regulators HSP-70.2 [48], [49] and cyclin A1 [50].

The sex-ratio distortion lead us to study the XY-bodies in pachytene spermatocytes from Alkbh1−/− testes, however visible XY-bodies were detected showing that X and Y chromosomes paired normally during male meiosis. This does not exclude the hypothesis of an epigenetic and silencing defect of the paternal X chromosome in those mice, which could explain the sex-ratio distortion observed. Moreover, embryonic and postnathal lethality seen in Alkbh1−/− mice seem to be of paternal origin and Alkbh1−/− males exhibit subfertility compared to wild-type males. Several characteristics of the Alkbh1−/− mice are comparable with those described for the Jmjd1a histone lysine demethylase and the G9a histone lysine methyltransferase mutant mice, although to a milder extent than demonstrated in the histone disrupted mouse models [51], [52]. Jmjd1a deficiency caused extensive germ cell apoptosis and blocked spermatid elongation, resulting in small testes and infertility in male mice [51]. Inactivation of G9a in the germ-lineage resulted in sterility due to a drastic loss of mature gametes [52]. The specific upregulation of Alkbh1 in the pachytene stage, together with the sex-ratio distortion, suggests a potential to regulate the expression of genes during meiosis in the germline. Future investigations will focus on the regulation of specific genes in pachytene spermatocytes isolated from Alkbh1−/− and wild-type testes.

Alkbh1 mutant mice displayed phenotypes of incomplete penetrance, including unilateral eye malformations, neural tube defects, and craniofacial and skeleton associated abnormalities. Around 10% of the Alkbh1−/− mice appeared relatively normal, whereas the most affected mice died early during embryogenesis. The phenotypes are similar to published results on the bone morphogenetic proteins (Bmps), such as haploinsufficiency of Bmp2 causing exencephaly comparable to Fig. 7A [53], and compound heterozygous mutants for Bmp2 and Bmp4 showing unilateral microphthalmia similar to Fig. 67 [54]. In addition, postnatal lethality and sex-ratio distortion against females have been shown in Bmp4tm1/+ heterozygous at weaning [55]. Altogether, this led us to investigate the effect on Bmps, and the misexpression of Bmp2, Bmp4 and Bmp7 in Alkbh1−/− embryos at E11.5 might explain the inconsistent phenotypes presented. This is due to the critical dependence of gene dosage for proper Bmp function together with the expression- and function-overlap of the Bmps in different tissues [39], [40]. Mouse models of Bmp4 and Bmp7 have shown that redundancy between Bmp4 and Bmp7 is not sufficient to prevent the eye phenotype to occur [40], [41], [56]. In the skull, signaling pathways involving Bmp2, Bmp4 and Bmp7 regulate mesenchymal condensation size, and intense expression of these signaling genes is necessary for closure of sutures [34]. In addition to modifier genes such as Bmps, genetic and epigenetic components can cause variable phenotypic outcomes from specific genes [57], leading to irregular patterns of inheritance as seen for the Alkbh1 deficient mice. A recent paper has shown that the osteoblast-specific transcription factor Osterix is regulated by the JmjC histone demethylase NO66 [58]. Experiments in the chick embryo have revealed that epigenetic factors are required for the establishment of left-right asymmetries, together with the action of well-studied genetic and signaling mechanisms [59], [60].

The reduced viability and developmental phenotypes apparent in our mouse model, was not reported in the Alkbh1-null mice generated by Pan et al [20]. However, they showed severe growth defects in Alkbh1−/− embryos and newborns in addition to placentas [20], and the growth retardation demonstrated in pups at four weeks of age are comparable with our data (Pan et al. Suppl. Fig. 2 and this paper Fig. S1). No obvious color variation (from red/pink to pale brown/bluish) or growth retardation was observed in Alkbh1−/− placentas compared to wild-type placentas. Our results are based on extensive breeding studies of Alkbh1 targeted mice, which revealed a dramatic effect on lethality and sex-ratio in adult mice. We therefore sought to characterize testes and embryos in more detail, as well as the prominent abnormalities in eye development. The different mouse background chosen as well as the dissimilar targeting strategies deleting different parts of the Alkbh1 gene (Exon 6 in our strain, Exon 3 in Pan et al) could be a possible explanation for the discrepancies in the penetrance of phenotypes in the two knockout mice models. Even so, together with the findings on Alkbh1 by Pan et al, these data suggest that the effect of Alkbh1 deficiency is pleiotropic and dependent on cell type and/or stage of development.

Recent studies have recognized roles for 2-oxoglutarate dependent dioxygenases in histone and nucleic acid demethylation, as well as in signaling protein hydroxylation [19]. For the demethylating enzymes, several have been shown to carry out its reaction in a manner similar to the potential Alkbh1 mediated, iron- and 2-oxoglutarate dependent, hydroxylation [1], [2], [61]. Previously, mouse models for histone methyl transferases and histone demethylases have been characterized with multiple developmental defects [31][33], [62]. Our working hypothesis, based on the variable developmental phenotype of Alkbh1 deficient mice together with the localization of Alkbh1 to nuclear euchromatin [20], is that Alkbh1 possibly works as a histone demethylase during embryogenesis and spermatogenesis. We believe that the hydroxylation activity of Alkbh1 is dependent on yet undefined partners specific for the different stages/tissues where it has an important role, and this will be addressed in future studies for the pachytene stage of meiosis in male germ cells – when homologues chromosomes pair and crossing over can occur.

Supporting Information

Figure S1

Average body weight of Alkbh1 targeted males and females. (A) 1-month old wild-type (19.0±2.0 g, n = 45) and Alkbh1−/− (14.6±3.8 g, n = 48) males, and 1-month old wild-type (17.7±1.7 g, n = 43) and Alkbh1−/− (14.8±2.2 g, n = 33) females. The average weight was 25% lower for Alkbh1−/− males than for wild-type males and 15% lower for Alkbh1−/− females than for wild-type females. About one out of five Alkbh1−/− males showed more than 40% lower weight compared to wild-type males. (B) 9-month old wild-type (40.5±4.2 g, n = 23) and Alkbh1−/− (32.5±2.9 g, n = 31) males, and 9-month old wild-type (31.5±3.4 g, n = 28) and Alkbh1−/− (29.3±3.8 g, n = 41) females. The average weight of Alkbh1−/− males was 20% below that of wild-type males, and the average weight of Alkbh1−/− females was 7% below that of wild-type females. No weight difference was demonstrated between the Alkbh1+/− and wild-type (data not shown). +/+ (wild-type), black bars; −/− (Alkbh1−/−), grey bars.

(0.10 MB TIF)

Figure S2

Closer view of the DAPI and TUNEL staining of testis sections shown in Fig. 4. (A, B) Sections from 9-month old wild-type (left panel) and Alkbh1−/− (right panel) mice are presented. Apoptosis was detected in degenerating spermatids (Sd) in the luminal layers of Alkbh1−/− tubules, as well as in severely degraded cells in the subbasal regions corresponding to spermatocytes and spermatids. No apoptotic cells were seen in spermatogonia (Sg) and spermatocytes (Sc) in Alkbh1−/− mice, although the amount of all spermatogenic cells are reduced in the apoptotic tubules. (Magnification: ×20).

(3.93 MB TIF)

Figure S3

Immunostaining with stage-specific antibodies against spermatogenic cells in Alkbh1 deficient testes. (A) Testis sections from 12-month old wild-type and Alkbh1−/− males stained with TRA98 antibody specific for spermatogonia, which were present both in wild-type and mutant. Although several tubules showed spermatogonia not only in the first basal layer, but also in the subbasal layers in the Alkbh1−/− mice, no significant differences were detected when compared to wild-type. (B) Testis sections from 12-month old wild-type and Alkbh1−/− males stained with TRA369 specific for pachytene spermatocytes through elongating spermatids, which were present both in wild-type and mutant. (Magnification: ×20).

(1.84 MB TIF)

Figure S4

Skeletal defects, eye defects in combination with NTD, and lens defects in Alkbh1 targeted mice. (A) Craniofacial defects. Dorsal view of the craniofacial skeleton of adult mice showing assymetric shortening of the nasal bones, curving unilaterally in Alkbh1−/− mice causing mal-developed teeth (n = 4 Alkbh1−/−; n = 1 Alkbh1+/−). Ossified areas are shown in red and cartilage in blue. (B) Limb defects. Dorsal view of the autopod limb skeleton revealing reduced ossification in the phalanges (P) and the metatarsals (M) of the autopod of Alkbh1−/− newborns (n = 4/4 Alkbh1−/−). Ossified areas are shown in black and cartilage in blue. (C) Eye defects and NTDs. Side view of embryos at E12.5. The Alkbh1−/− embryo has a bilateral microphthalmic eye phenotype in combination with a neural tube defect (NTD). The NTD is originating from disrupted closure in the upper spinal region, and is associated with head and facial malformations leading to a shortened, broad snout. In addition, a severe intracranial hemorrhage is visible. (D) Lens defects. Histological analysis of paraffin-embedded eye sections from adult mice. In Alkbh1−/− eyes the lens fiber cells have lost their ordered lamination pattern, and swollen and liquefied fibers as well as vacuoles are seen throughout the lens. (Magnification: ×10).

(6.28 MB TIF)

Table S1

Statistically upregulated genes in Alkbh1−/− versus wild-type testes identified in the microarray analysis. Microarray analysis of RNA extracted from whole testes from three wild-type and three Alkbh1−/− 12-week old males identified 6 genes that were statistically upregulated in Alkbh1−/− versus wild-type. To find differentially expressed genes, t-test with randomized variance was used as statistical test and the cut-off (p-value) was set to 0.05 with a FDR correction.

(0.22 MB TIF)


We are grateful to Hege Wiksèn, Cecilie G. Castellanos, Linda Ellevog and Gaute Nesse for excellent technical assistance. We thank IngenKO, Australia, The Norwegian Transgenic Center (NTS) and the Centre for Comparative Medicine at Oslo University Hospital for the excellent service they provided.


Competing Interests: The authors have declared that no competing interests exist.

Funding: This work was supported by the National Program in Functional Genomics (FUGE) sponsored by the Norwegian Research Council, the Norwegian Cancer Society and the European Union program ‘DNA repair’. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.


1. Trewick SC, Henshaw TF, Hausinger RP, Lindahl T, Sedgwick B. Oxidative demethylation by Escherichia coli AlkB directly reverts DNA base damage. Nature. 2002;419:174–178. [PubMed]
2. Falnes PO, Johansen RF, Seeberg E. AlkB-mediated oxidative demethylation reverses DNA damage in Escherichia coli. Nature. 2002;419:178–182. [PubMed]
3. Kurowski MA, Bhagwat AS, Papaj G, Bujnicki JM. Phylogenomic identification of five new human homologs of the DNA repair enzyme AlkB. BMC Genomics. 2003;4:48. [PMC free article] [PubMed]
4. Falnes PO, Klungland A, Alseth I. Repair of methyl lesions in DNA and RNA by oxidative demethylation. Neuroscience. 2007;145:1222–1232. [PubMed]
5. Lee DH, Jin SG, Cai S, Chen Y, Pfeifer GP, et al. Repair of methylation damage in DNA and RNA by mammalian AlkB homologues. J Biol Chem. 2005;280:39448–39459. [PubMed]
6. Duncan T, Trewick SC, Koivisto P, Bates PA, Lindahl T, et al. Reversal of DNA alkylation damage by two human dioxygenases. Proc Natl Acad Sci U S A. 2002;99:16660–16665. [PubMed]
7. Aas PA, Otterlei M, Falnes PO, Vagbo CB, Skorpen F, et al. Human and bacterial oxidative demethylases repair alkylation damage in both RNA and DNA. Nature. 2003;421:859–863. [PubMed]
8. Sedgwick B. Repairing DNA-methylation damage. Nat Rev Mol Cell Biol. 2004;5:148–157. [PubMed]
9. Monsen VT, Sundheim O, Aas PA, Westbye MP, Sousa MM, et al. Divergent {beta}-hairpins determine double-strand versus single-strand substrate recognition of human AlkB-homologues 2 and 3. Nucleic Acids Res. 2010 gkq518 [pii];10.1093/nar/gkq518 [doi]. [PMC free article] [PubMed]
10. Ringvoll J, Nordstrand LM, Vagbo CB, Talstad V, Reite K, et al. Repair deficient mice reveal mABH2 as the primary oxidative demethylase for repairing 1meA and 3meC lesions in DNA. EMBO J. 2006;25:2189–2198. [PubMed]
11. Fu D, Brophy JA, Chan CT, Atmore KA, Begley U, et al. Human AlkB homolog ABH8 Is a tRNA methyltransferase required for wobble uridine modification and DNA damage survival. Mol Cell Biol. 2010;30:2449–2459. [PMC free article] [PubMed]
12. Songe-Moller L, van den BE, Leihne V, Vagbo CB, Kristoffersen T, et al. Mammalian ALKBH8 possesses tRNA methyltransferase activity required for the biogenesis of multiple wobble uridine modifications implicated in translational decoding. Mol Cell Biol. 2010;30:1814–1827. [PMC free article] [PubMed]
13. Shimada K, Nakamura M, Anai S, De VM, Tanaka M, et al. A novel human AlkB homologue, ALKBH8, contributes to human bladder cancer progression. Cancer Res. 2009;69:3157–3164. 0008-5472.CAN-08-3530 [pii];10.1158/0008-5472.CAN-08-3530 [doi]. [PubMed]
14. Gerken T, Girard CA, Tung YC, Webby CJ, Saudek V, et al. The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase. Science. 2007;318:1469–1472. [PMC free article] [PubMed]
15. Boissel S, Reish O, Proulx K, Kawagoe-Takaki H, Sedgwick B, et al. Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations. Am J Hum Genet. 2009;85:106–111. S0002-9297(09)00238-9 [pii];10.1016/j.ajhg.2009.06.002 [doi]. [PubMed]
16. Han Z, Niu T, Chang J, Lei X, Zhao M, et al. Crystal structure of the FTO protein reveals basis for its substrate specificity. Nature. 2010;464:1205–1209. nature08921 [pii];10.1038/nature08921 [doi]. [PubMed]
17. Westbye MP, Feyzi E, Aas PA, Vagbo CB, Talstad VA, et al. Human AlkB homolog 1 is a mitochondrial protein that demethylates 3-methylcytosine in DNA and RNA. J Biol Chem. 2008;283:25046–25056. [PMC free article] [PubMed]
18. Sedgwick B, Robins P, Lindahl T. Direct removal of alkylation damage from DNA by AlkB and related DNA dioxygenases. Methods Enzymol. 2006;408:108–120. [PubMed]
19. Loenarz C, Schofield CJ. Expanding chemical biology of 2-oxoglutarate oxygenases. Nat Chem Biol. 2008;4:152–156. [PubMed]
20. Pan Z, Sikandar S, Witherspoon M, Dizon D, Nguyen T, et al. Impaired placental trophoblast lineage differentiation in Alkbh1(−/−) mice. Dev Dyn. 2008;237:316–327. [PubMed]
21. Tsujikawa K, Koike K, Kitae K, Shinkawa A, Arima H, et al. Expression and sub-cellular localization of human ABH family molecules. J Cell Mol Med. 2007;11:1105–1116. [PubMed]
22. Bellve AR. Purification, culture, and fractionation of spermatogenic cells. Methods Enzymol. 1993;225:84–113. [PubMed]
23. Kataoka H, Yamamoto Y, Sekiguchi M. A new gene (alkB) of Escherichia coli that controls sensitivity to methyl methane sulfonate. J Bacteriol. 1983;153:1301–1307. [PMC free article] [PubMed]
24. Taylor DR, Ingvarsson PK. Common features of segregation distortion in plants and animals. Genetica. 2003;117:27–35. [PubMed]
25. Solari AJ. The behavior of the XY pair in mammals. Int Rev Cytol. 1974;38:273–317. [PubMed]
26. Avraham S, London R, Tulloch GA, Ellis M, Fu Y, et al. Characterization and chromosomal localization of PTPRO, a novel receptor protein tyrosine phosphatase, expressed in hematopoietic stem cells. Gene. 1997;204:5–16. [PubMed]
27. Beltran PJ, Bixby JL, Masters BA. Expression of PTPRO during mouse development suggests involvement in axonogenesis and differentiation of NT-3 and NGF-dependent neurons. J Comp Neurol. 2003;456:384–395. [PubMed]
28. Kawakatsu T, Ogita H, Fukuhara T, Fukuyama T, Minami Y, et al. Vav2 as a Rac-GDP/GTP exchange factor responsible for the nectin-induced, c-Src- and Cdc42-mediated activation of Rac. J Biol Chem. 2005;280:4940–4947. [PubMed]
29. Liu Y, Monticone M, Tonachini L, Mastrogiacomo M, Marigo V, et al. URB expression in human bone marrow stromal cells and during mouse development. Biochem Biophys Res Commun. 2004;322:497–507. [PubMed]
30. Graw J. The genetic and molecular basis of congenital eye defects. Nat Rev Genet. 2003;4:876–888. [PubMed]
31. Rizzoti K, Lovell-Badge R. SOX3 activity during pharyngeal segmentation is required for craniofacial morphogenesis. Development. 2007;134:3437–3448. [PubMed]
32. Chang B, Chen Y, Zhao Y, Bruick RK. JMJD6 is a histone arginine demethylase. Science. 2007;318:444–447. [PubMed]
33. Bose J, Gruber AD, Helming L, Schiebe S, Wegener I, et al. The phosphatidylserine receptor has essential functions during embryogenesis but not in apoptotic cell removal. J Biol. 2004;3:15. [PMC free article] [PubMed]
34. Hall BK, Miyake T. All for one and one for all: condensations and the initiation of skeletal development. Bioessays. 2000;22:138–147. [PubMed]
35. Glazier AM, Nadeau JH, Aitman TJ. Finding genes that underlie complex traits. Science. 2002;298:2345–2349. [PubMed]
36. Copp AJ, Greene ND, Murdoch JN. The genetic basis of mammalian neurulation. Nat Rev Genet. 2003;4:784–793. [PubMed]
37. Robert B. Bone morphogenetic protein signaling in limb outgrowth and patterning. Dev Growth Differ. 2007;49:455–468. [PubMed]
38. Baldridge D, Shchelochkov O, Kelley B, Lee B. Signaling pathways in human skeletal dysplasias. Annu Rev Genomics Hum Genet. 2010;11:189–217. 10.1146/annurev-genom-082908-150158 [doi]. [PubMed]
39. Bandyopadhyay A, Tsuji K, Cox K, Harfe BD, Rosen V, et al. Genetic analysis of the roles of BMP2, BMP4, and BMP7 in limb patterning and skeletogenesis. PLoS Genet. 2006;2:e216. [PubMed]
40. Ducy P, Karsenty G. The family of bone morphogenetic proteins. Kidney Int. 2000;57:2207–2214. [PubMed]
41. Ohkubo Y, Chiang C, Rubenstein JL. Coordinate regulation and synergistic actions of BMP4, SHH and FGF8 in the rostral prosencephalon regulate morphogenesis of the telencephalic and optic vesicles. Neuroscience. 2002;111:1–17. [PubMed]
42. Wordinger RJ, Clark AF. Bone morphogenetic proteins and their receptors in the eye. Exp Biol Med (Maywood) 2007;232:979–992. 232/8/979 [pii];10.3181/0510-MR-345 [doi]. [PubMed]
43. Deng W, Lin H. miwi, a murine homolog of piwi, encodes a cytoplasmic protein essential for spermatogenesis. Dev Cell. 2002;2:819–830. [PubMed]
44. Martianov I, Fimia GM, Dierich A, Parvinen M, Sassone-Corsi P, et al. Late arrest of spermiogenesis and germ cell apoptosis in mice lacking the TBP-like TLF/TRF2 gene. Mol Cell. 2001;7:509–515. [PubMed]
45. Zhang D, Penttila TL, Morris PL, Teichmann M, Roeder RG. Spermiogenesis deficiency in mice lacking the Trf2 gene. Science. 2001;292:1153–1155. [PubMed]
46. Ruggiu M, Speed R, Taggart M, McKay SJ, Kilanowski F, et al. The mouse Dazla gene encodes a cytoplasmic protein essential for gametogenesis. Nature. 1997;389:73–77. [PubMed]
47. Tanaka SS, Toyooka Y, Akasu R, Katoh-Fukui Y, Nakahara Y, et al. The mouse homolog of Drosophila Vasa is required for the development of male germ cells. Genes Dev. 2000;14:841–853. [PubMed]
48. Dix DJ, Allen JW, Collins BW, Mori C, Nakamura N, et al. Targeted gene disruption of Hsp70-2 results in failed meiosis, germ cell apoptosis, and male infertility. Proc Natl Acad Sci U S A. 1996;93:3264–3268. [PubMed]
49. Zhu D, Dix DJ, Eddy EM. HSP70-2 is required for CDC2 kinase activity in meiosis I of mouse spermatocytes. Development. 1997;124:3007–3014. [PubMed]
50. Liu D, Matzuk MM, Sung WK, Guo Q, Wang P, et al. Cyclin A1 is required for meiosis in the male mouse. Nat Genet. 1998;20:377–380. [PubMed]
51. Liu Z, Zhou S, Liao L, Chen X, Meistrich M, et al. The Jmjd1a demethylase-regulated histone modification is essential for crem-regulated gene expression and spermatogenesis. J Biol Chem 2009 [PMC free article] [PubMed]
52. Tachibana M, Nozaki M, Takeda N, Shinkai Y. Functional dynamics of H3K9 methylation during meiotic prophase progression. EMBO J. 2007;26:3346–3359. [PubMed]
53. Castranio T, Mishina Y. Bmp2 is required for cephalic neural tube closure in the mouse. Dev Dyn. 2009;238:110–122. [PMC free article] [PubMed]
54. Uchimura T, Komatsu Y, Tanaka M, McCann KL, Mishina Y. Bmp2 and Bmp4 genetically interact to support multiple aspects of mouse development including functional heart development. Genesis. 2009;47:374–384. [PMC free article] [PubMed]
55. Dunn NR, Winnier GE, Hargett LK, Schrick JJ, Fogo AB, et al. Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4. Dev Biol. 1997;188:235–247. [PubMed]
56. Wyatt AW, Osborne RJ, Stewart H, Ragge NK. Bone morphogenetic protein 7 (BMP7) mutations are associated with variable ocular, brain, ear, palate, and skeletal anomalies. Hum Mutat. 2010;31:781–787. 10.1002/humu.21280 [doi]. [PubMed]
57. van Heyningen V, Yeyati PL. Mechanisms of non-Mendelian inheritance in genetic disease. Hum Mol Genet 13 Spec No. 2004;2:R225–R233. [PubMed]
58. Sinha KM, Yasuda H, Coombes MM, Dent SY, de CB. Regulation of the osteoblast-specific transcription factor Osterix by NO66, a Jumonji family histone demethylase. EMBO J. 2010;29:68–79. emboj2009332 [pii];10.1038/emboj.2009.332 [doi]. [PMC free article] [PubMed]
59. Raya A, Kawakami Y, Rodriguez-Esteban C, Ibanes M, Rasskin-Gutman D, et al. Notch activity acts as a sensor for extracellular calcium during vertebrate left-right determination. Nature. 2004;427:121–128. [PubMed]
60. Wang S, Yu X, Zhang T, Zhang X, Zhang Z, et al. Chick Pcl2 regulates the left-right asymmetry by repressing Shh expression in Hensen's node. Development. 2004;131:4381–4391. [PubMed]
61. Tsukada Y, Fang J, Erdjument-Bromage H, Warren ME, Borchers CH, et al. Histone demethylation by a family of JmjC domain-containing proteins. Nature. 2006;439:811–816. [PubMed]
62. Li MO, Sarkisian MR, Mehal WZ, Rakic P, Flavell RA. Phosphatidylserine receptor is required for clearance of apoptotic cells. Science. 2003;302:1560–1563. [PubMed]

Articles from PLoS ONE are provided here courtesy of Public Library of Science