- Research article
- Open Access
The DEAD-box protein MEL-46 is required in the germ line of the nematode Caenorhabditis elegans
© Minasaki et al; licensee BioMed Central Ltd. 2009
Received: 27 June 2008
Accepted: 17 June 2009
Published: 17 June 2009
In the hermaphrodite of the nematode Caenorhabditis elegans, the first germ cells differentiate as sperm. Later the germ line switches to the production of oocytes. This process requires the activity of a genetic regulatory network that includes among others the fem, fog and mog genes. The function of some of these genes is germline specific while others also act in somatic tissues. DEAD box proteins have been shown to be involved in the control of gene expression at different steps such as transcription and pre-mRNA processing.
We show that the Caenorhabditis elegans gene mel-46 (maternal effect lethal) encodes a DEAD box protein that is related to the mammalian DDX20/Gemin3/DP103 genes. mel-46 is expressed throughout development and mutations in mel-46 display defects at multiple developmental stages. Here we focus on the role of mel-46 in the hermaphrodite germ line. mel-46(yt5) mutant hermaphrodites are partially penetrant sterile and fully penetrant maternal effect lethal. The germ line of mutants shows variable defects in oogenesis. Further, mel-46(yt5) suppresses the complete feminization caused by mutations in fog-2 and fem-3, two genes that are at the top and the center, respectively, of the genetic germline sex determining cascade, but not fog-1 that is at the bottom of this cascade.
The C. elegans gene mel-46 encodes a DEAD box protein that is required maternally for early embryogenesis and zygotically for postembryonic development. In the germ line, it is required for proper oogenesis. Although it interacts genetically with genes of the germline sex determination machinery its primary function appears to be in oocyte differentiation rather than sex determination.
The exact mode of action of the six mog genes is not known. In addition to their function in germline sex determination, they are also maternally required for embryonic viability [14, 15]. Three of the four mog genes that have been cloned so far encode DEAH box RNA helicases, namely, MOG-1, MOG-4 and MOG-5, which are the homologs of yeast splicing factors PRP16, PRP2, and PRP22, respectively [21, 22]. Also ddx-23, which encodes a DEAD box protein homolgous to the yeast splicing factor PRP28 was found to be required for the sperm/oocyte switch .
DEAH and DEAD box proteins belong to the DExD/H RNA helicase family, which play many roles in RNA metabolism, for example, pre-mRNA splicing, ribosome biogenesis, RNA transport, translation initiation, and RNA decay [24–26]. Recently, the classical view that DExD/H proteins are exclusively involved in RNA metabolism was contested by evidence that several DExD/H proteins show non-RNA related activities that do not require their highly conserved helicase core motifs . In C. elegans, several DEAD box RNA helicases are involved in germ line development. Loss of glh-1 and glh-4 (Germ line RNA Helicase) gene functions cause sterility due to failure in oogenesis and spermatogenesis [28, 29]. Increased germline apoptosis was observed in the cgh-1 (Conserved Germline Helicase) mutant . mut-14 encodes yet another DEAD box helicase and is essential for germ line transposon inactivation and post-transcriptional gene silencing . Other DEAD box RNA helicases are components of the P-granules , which are germ cell specific structures . P-granules are considered to be pivotal for RNA metabolism as they contain many structural RNAs [34, 35] and proteins involved in pre-mRNA splicing, RNA decay and translational activation [36–38]. The exact nature of how these DEAD box RNA helicases participate in the various features of germline development in C. elegans remains elusive.
In total, thirty-seven DEAD box and 11 DEAH box proteins are encoded in the C. elegans genome . Systematic analysis of RNAi phenotypes suggested that more than half of these genes are essential and many are required for multiple developmental processes. However, for only a few of these genes has the characterization of mutants been reported. Here we describe a previously uncharacterized DEAD box protein-encoding gene, mel-46. Loss of mel-46 results in defects in several aspects of development. In this study, we particularly focus on the requirement for mel-46 in the germ line.
Caenorhabditis elegansstrains and culture
The strain names and the full genotypes of the worm strains used were:
N2: Standard wild-type strain,
CB4856: polymorphic wild-type strain from Hawaii,
AH35: unc-119(e2498)III; zhIs1[unc-119(+) + lin-39::GFP],
BC1227: sDf23/nT1 IV; +/nT1 V,
FR695: sw1s15[ceh-13(enh740)::gfp + rol-6(su1006)dm]V,
QA3: egl-38(n578) mec-3(n3197)IV; sw1s15[ceh-13(enh740)::gfp + rol-6(su1006)dm]V,
QA243: mel-46(yt5) IV; yDp1(IV;f),
QA269: ytEx209[pRM8 (mel-46 rescue) + sur-5::gfp]; mel-46(yt5)IV,
QA270: ytEx210[pRM8 (mel-46 rescue) + sur-5::gfp]; mel-46(yt5)IV,
QA273: ytEx211[pRM8 (mel-46 rescue) + sur-5::gfp]; mel-46(tm1739)IV,
QA298: fem-3(e2006ts) mel-46(yt5)IV,
QA300: mel-46(yt5)/nT1IV; +/nT1V,
Standard techniques of molecular biology were performed as described .
The specimens were prepared and analyzed following standard procedures . For microscopy we used a Zeiss Axioplan 2 microscope fitted with a digital camera (MicroMax 5 MHz System, Princeton Instruments, Inc) or a Zeiss Axio Imager microscope with a SPOT camera (Diagnostic Instruments, Inc). Both microscopy setups were operated through the program MetaMorph (version 6.2r4 Universal Imaging Corporation™). The images were processed using either MetaMorph (version 6.2r4, Universal Imaging Corporation™) or Axiovision (release 4.2) and Adobe Photoshop (version 7.0).
Isolation, backcrossing and balancing of the mutations mel-46(yt5) and mel-46(tm1739)
The mutation mel-46(yt5ts) was isolated in a screen for mutations that cause alterations in ceh-13::gfp (enh740::gfp) expression . Prior to analysis the strain was backcrossed to N2 10 times. During this process the transgene sw1s15[ceh-13(enh740)::gfp + rol-6(su1006)dm]V was removed from the strain. The mutation was balanced over nT1 (strain QA300), with the free duplication yDp1 (strain QA243) or the rescuing extrachromosomal arrays ytEx209 (strain QA269) or ytEx210 (QA270). Temporarily, the mutation was also maintained homozygously at permissive temperature between 15°C and 20°C. The deletion allele mel-46(tm1739) was generated by the National Bioresource Project for Caenorhabditis elegans in Japan upon our request and was sent to us by Dr S. Mitani. The mutation was backcrossed 10 times with N2 and balanced over the rescuing transgene ytEx211 resulting in strain QA273. This deletion starts at codon 173 of the predicted protein and removes part of exon 4 (41 bp), the entire intron 4 (65 bp) and exon 5 (125 bp) and part of intron 5 (194 bp).
Sterility assay and dissection and DAPI staining of gonads
mel-46(yt5)/+ hermaphrodites were raised at 20°C and 25°C. Individual L1/L2 larvae were placed onto new plates and kept at the respective temperatures. Alternatively, progeny of mel-46(yt5) homozygous animals that had been raised at 15°C were picked and shifted to 25°C. After two days the plates were inspected. Animals that had not laid any embryos were considered sterile and animals that had laid all unhatched embryos were considered maternal effect lethal (Mel). Some of the adults were chosen randomly and their gonads dissected. The gonads were fixed in cold Methanol for 5 minutes at -20°C, transferred to PBS and DAPI (diamidinophenylindole) was added at a concentration of 1 μg/ml for 10 minutes.
Determining gonad defects in sterile animals
Sterile non-transgenic animals of the strain QA269 were raised at 25°C and examined either by Nomarski DIC microscopy or by epi-illumination fluorescence after DAPI staining. 40× and 100× objectives were used for both types of microscopy.
Brood size analysis
We placed progeny of mel-46(yt5)/+ mothers raised at either 15, 20, 23, or 25°C individually onto plates that were at the respective growth temperature. All animals were taken from cultures that had been maintained at their respective temperatures for at least two generations. Every day these animals were transferred to new plates and the embryos they produced were counted. Animals that produced no embryos were considered to be sterile, those that produced only or mainly dying embryos were considered to be Mel. Mel and sterile animals were considered to be mel-46(yt5) homozygotes. Worms that produced viable progeny were considered to be mel-46(yt5)/+ or +/+. The data for each temperature are the sum of three independent experiments.
Construction and analysis of double mutant strains with fem-3(e2006), fog-1(q253) and fog-2(q71)
The double mutants were constructed as follows.
QA298: fem-3(e2006ts) mel-46(yt5ts)IV: We crossed CB3844:fem-3(e2006ts) hermaphrodites with mel-46(yt5) males at 15°C. The F1 progeny were cultured at 25°C and allowed to reproduce by self-fertilization. F2 animals were kept individually at 25°C until 24 h after they had laid the first embryos. Mel animals (mel-46(yt5) homozygotes) were shifted to 15°C in order to produce viable F3 animals. Later we lysed the F2 animals and searched for the recombinant genotype [mel-46(yt5) fem-3(e2006)/mel-46(yt5) +] by PCR and sequencing. The mel-46(yt5) fem-3(e2006) chromosome was made homozygous at 15°C in the following generations and the genotype confirmed. Note: the only molecular lesion we found in fem-3(e2006) was (AGT to AUA: Met129 to Ile) and not (AGT to AUA: Met159 to Ile) as originally reported . We assume that it is due to a typing error in the original publication.
QA310: fog-1(q253ts)I; mel-46(yt5ts)IV: JK560:fog-1(q253ts)I hermaphrodites were crossed with mel-46(yt5) males at 15°C. The F1 generation was raised at 25°C and allowed to reproduce by self-fertilization. F2 animals were kept individually at 25°C until 24 hours after they had laid the first embryos. Mel animals (mel-46(yt5) homozygotes) were shifted to 15°C in order to produce viable F3 animals. F3 animals were picked individually to plates and double homozygous strains identified by PCR and sequencing of the molecular lesions.
QA311: mel-46(yt5)IV; fog-2(q71)V: JK574:fog-2(q71) females were crossed with mel-46(yt5) males at 15°C. The F1 animals were shifted to 25°C and F2 animals were raised at 25°C individually. Mel non Fog F2 animals were selected and shifted down to 15°C and allowed to reproduce by self-fertilization. Female F3 animals [mel-46(yt5)/mel-46(yt5); fog-2(q71)/fog-2(q71)] were crossed with fog-2(q71) males at 15°C. The resulting [mel-46(yt5)/+; fog-2(q71)/fog-2(q71)] males and females were crossed. In the next generation cultures were started with single pair crosses and double homozygous animals were identified by analysis of both molecular lesions.
Analysis of the mutant strains
A large number of the double mutants as well as the corresponding single mutant strains and the wild-type N2 strain were cultured at 15°C, then embryos were isolated by hypochloride treatment . The embryos were cultured at 15°C for 12 hours before the hatched L1 larvae were transferred individually to plates and shifted to 25°C where they were incubated for 48 hours. We then searched for embryos that were present on the plates. Double mutants that produced embryos were kept and the total number of embryos they produced was determined. The data for each set (double mutant, single mutants, and wild type) are the sum of three independent experiments. In each experiment, all four strains were analyzed in parallel.
Cloning of mel-46
We determined the approximate location of mel-46(yt5) at the right of linkage group IV by bulk segregant analysis single nucleotide polymorphism (SNP) mapping . We then created strain dpy-4(e1166)mel-46(yt5) by interbreeding CB1166: dpy-4(e1166) and mel-46(yt5) and selecting double homozygotes in the F3 generation based on the Dpy and the Mel phenotypes (later this strain was unfortunately lost). We crossed dpy-4(e1166)mel-46(yt5) hermaphrodites with CB4856 males and allowed the progeny to reproduce by self-fertilization. In the next generation we selected Dpy non Mel animals for SNP analysis, which allowed us to place mel-46(yt5) very close to the right of a SNP (snp_Y43D4) at the physical position 16728927. Direct sequencing of candidate genes from the mel-46(yt5) mutant genomic DNA revealed a premature stop (C168560033T, Q907Ochre) in the predicted gene T06A10.1. This mutation is neither present in the parental strain QA3 nor in the wild type strain N2. The small deletion allele tm1739 in T06A10.1 (see above) failed to complement mel-46(yt5) (see below). Further we were able to phenocopy the Mel-46(yt5) phenotype by RNAi (see below) and to rescue all aspects of the phenotypes of both mutations with a transgene where T06A10.1 was the only open reading frame (Plasmid pRM8 see below, strains QA269, QA270 and QA273).
yt5 and tm1739
Wild type N2 hermaphrodites were crossed with QA158: mel-46(yt5) homozygous males, which had been growing at 15°C. The resulting males [+/mel-46(yt5)] were crossed with QA273: ytEx211 [pRM8:mel-46(+) + sur-5::gfp]; mel-46(tm1739)IV hermaphrodites. The SUR-5::GFP negative hermaphrodite progeny were picked at L1 stage and transferred to 25°C. The genotypes of these worms are expected to be 1/2 +/mel-46(tm1739) and 1/2 mel-46(tm1739)/mel-46(yt5). Of the 63 animals analyzed 32 gave rise to viable progeny and we confirmed that their genotype was +/mel-46(tm1739) by PCR and by following the phenotypes in the next generation. The remaining 31 animals showed a fully penetrant Mel phenotype if they produced embryos and we confirmed that their genotype was mel-46(tm1739)/mel-46(yt5)] by PCR. This indicates that yt5 and tm1739 are allelic.
yt5 and ok1475
RB1343: T06A10.4(ok1475) hermaphrodites were crossed with mel-46(yt5) homozygous males, which had been raised at 15°C. None of the F1 progeny showed a Mel phenotype (n > 30) at 25°C. We further confirmed the genotype by PCR. Therefore yt5 and ok1475 are not allelic.
tm1739 and ok1475
QA273: ytEx211 [pRM8 (mel-46 rescue)+sur-5::gfp]; mel-46(tm1739) IV hermaphrodites were crossed with wild type males to obtain [+/mel-46(tm1739)]. The SUR-5::GFP negative males were then crossed with RB1343: T06A10.4(ok1475). The genotypes of the cross progeny should be 1/2 [+/T06A10.4(ok1475)] and 1/2 [mel-46(tm1739)/T06A10.4(ok1475)]. We determined the genotype of 30 cross progeny by PCR and sequencing and found 14 to be [+/T06A10.4(ok1475)] and 16 to be [mel-46(tm1739)/T06A10.4(ok1475)]. All these animals grew normally and produced viable progeny. Therefore tm1739 and ok1475 are not allelic.
yt5 and sDf23
BC1227: sDf23/nT1 IV; +/nT1 V hermaphrodites were crossed with the mel-46(yt5) homozygous males at 15°C. From the plates that had males we single-picked 80 F1 hermaphrodites and placed them at 25°C. None of these F1 hermaphrodites showed a Mel phenotype. As a control we followed the next generation of four randomly selected F1s and confirmed that mel-46(yt5) was present, showing that the original cross was efficient. This indicates that sDf23 does not uncover yt5.
yt5 and cyk-2(oj34)
WH145: cyk-2(oj34ts) IV hermaphrodites were crossed with mel-46(yt5) males at 15°C. We picked many F1 progeny (n > 100) from the plates that had males and transferred them individually to new plates and shifted them to 25°C. The resulting F1 produced showed no Mel phenotype. This indicates that yt5 and cyk-2(oj34ts) are not allelic.
Double stranded RNA interference (RNAi)
We purchased the T06A10.1 RNAi clone from Geneservice Ltd . The clone contains 1135 base pairs of genomic sequence (physical position 16858332 to 16859466) flanked by T7 promoters. We amplified the T06A10.1 region by PCR with T7 promoter primers and used the product as template for in vitro transcription using the MEGAscript® (Ambion) kit following the manufacturer's instructions. The resulting transcripts were heated to 95° for 5 minutes, then annealed at room temperature to produce double stranded RNA. The RNA was diluted in water to approximately 0.5 μg/μl and injected into the gonads of L4 or young adult hermaphrodites as described . The injected worms were transferred to new plates 12 hours after injection and the progeny they produced was analyzed 24 to 36 hours after transfer.
Extrachromosomal transgenes were obtained by micro-injection of DNA into the gonad of adult hermaphrodite worms . The following concentrations were used to make extra-chromosomal arrays: ytEx209 and ytEx210, ytEx211 (pRM8 at 133 ng/μl and pTG96(sur-5::GFP) at 80 ng/μl) .
Determination of the mel-46cDNA sequence
Total RNA was isolated from mixed staged worms using the Qiagen midi total RNA Kit (Cat. number 75142) according to the manufacturer's instructions. Reverse transcription was carried out with SuperScript™ II Reverse Transcriptase (Invitrogen) according to the manufacturer's instructions with random hexamer primers (for the 5' RACE) or primer BJ796 (5'-CCAGTGAGCAGAGTGACGAGGACTCGAGCTCAAGCT15V-3') (for the 3' RACE). One μl of the reverse transcription reaction was used as template for first round of PCR (30 cycles of 94° for 1 minute, 58° for 1 minute and 68° for 1 minute) using a primer against SL1 (for 5' RACE) or a primer that is complementary to BJ796 and different internal primers. One μl of the first round PCR was used as template for a second round of PCR with nested primers. A full list of all the primers used for the RACE experiments is available upon request. Two overlapping partial cDNA clones were generated. pRM3: a 1754 bp fragment extending from the splice leader SL1 to exon 8 was amplified using primers RM589-5'-GGTTCCTCTGTAAAATCGAATTTCGTC-3' and RS234-5'-GGTTTAATTACCCAAGTTTGAG-3' and cloned into TOPO pCR4 (Invitrogen). pRM5: a 2919 bp fragment ranging from exon 1 to the poly(A) tail was amplified using primers RM698- 5'-GAAAAATAGCCAATTCGACAGG-3' and BJ797 (see above) and cloned into TOPO pCR4 clones (Invitrogen). The full-length cDNA clone pRM7 was created by replacing the NotI (in the pCR4 vector) – SalI (in exon 5) fragment of pRM5 with the NotI – SalI fragment of pRM3. The full-length mel-46 cDNA is 2922 bp.
GenBank accession number
The accession number for the full-length mel-46 cDNA sequence is [GenBank:EU051652].
Making of mel-46rescue constructs
The NotI (in the vector) – SalI (in exon 5) fragment of pRM7, the clone that contains the full length mel-46 cDNA, was replaced with the genomic NotI-SalI fragment that extends from 1759 bp upstream of the translational start codon to exon 5. The genomic fragment was created by PCR amplification with primers RM1033-TATAGCGGCCGCTGCATGTGAAGTGGAACCAT and RM1031-ACCAGCGTTAAACCGAACAA followed by the restriction digestion with NotI and SalI. The resulting plasmid pRM8 hence consists of 1759 bp promoter, exons and introns 1 – 4, exons 5 – 10 and the mel-46 3'UTR in the backbone of TOPO pCR4.
Anti-MEL-46 antibody and Western Blotting
A Polyclonal anti-MEL-46 antibody was raised against the peptide CPFEERLRRQRKREK (AA724–739) and affinity purified by Biogenes, Berlin. For Western blotting, approximately 100 μl of worms were harvested and dissolved in 500 μl of sample buffer (Tris-HCl 60 mM, 25% Glycerol, 2% SDS, 14.4 mM Beta-marcaptoethanol) by boiling for five minutes. After adjusting the approximate concentration of the protein samples, 5–10 μl per lane were loaded onto standard SDS-PAGE gels. These gels were blotted onto Hybond-P Nylon membranes (Amersham Bioscience) according to the manufacturers' instructions. For detection the anti-MEL-46 antibodies were used at 1:2500. For the loading control, a polyclonal anti-alpha-tubulin antibody (Dianova, Hamburg) was used at 1:2500. As secondary antibody, we used an alkaline phosphatase conjugated goat anti-rabbit antibody from Dianova (Hamburg) at 1:1000 dilution and we detected the signals using the premixed PCIP/NBT solution (Sigma) according to manufacturer's instructions.
Isolation of the mutation yt5
mel-46encodes a putative DEAD box RNA helicase
MEL-46 is expressed throughout development
In situ hybridization images available from the Nematode Expression Pattern Database (http://nematode.lab.nig.ac.jp/; clone 90g5, accession numbers D74979 and D72164) show a strong signal in the gonad of the adult and in young embryos, which indicates that the RNA is present at these stages. Quantitative RT-PCR experiments confirmed this finding but also showed that the RNA is not restricted to adults and embryos and is also in the somatic tissues of adults (data not shown). To determine when and where the MEL-46 protein is present, we raised an antibody against an oligo-peptide (Fig 4B). On western blots the antibody recognizes a band above the 130 kD marker in extracts from wild type (N2) worms (Fig 5). In mel-46(yt5) mutants there is a novel band below the 130 kD marker. In extracts from worms that were homozygous for mel-46(yt5) and carried a wild type copy of the gene on a rescuing transgene, both bands are visible. Finally, in worms that are homozygous for the putative null allele mel-46(tm1739) and rescued by a transgene, only the wild type band is visible. This shows that the antibody recognizes MEL-46 and that the truncated protein is present in the yt5 mutants.
mel-46(yt5)is a partially penetrant temperature sensitive sterile allele
Temperature dependent sterility of mel-46(yt5) hermaphrodites
Sterile among mutant
Temperature dependent germline defects in mel-46(yt5) mutants
+/+ or mel-46(yt5)/ +
+/+ or mel-46(yt5)/ +
Class 2: a more severely disorganized arrangement of germ nuclei. Sperm, spermatocytes and ooids were mixed within the same region of the gonad (Fig 7D). Typically ooid nuclei had not entered diakinesis. Four (7%) of the 57 gonadal arms belonged to this class.
Class 3: worms with gonads that were much smaller than normal. Gonadal arms were thinner and contained less than 130 nuclei in mitosis or in meiotic prophase. Neither oocytes nor ooids have been observed in these germ lines (Fig 7E). Two (3.5%) of the 57 gonadal arms belonged to this class.
Temperature dependent decrease in brood size of mel-46(yt5) mutants
+/+ or mel-46(yt5)/ +
+/+ or mel-46(yt5)/ +
+/+ or mel-46(yt5)/ +
+/+ or mel-46(yt5)/ +
mel-46(yt5)weakly suppresses some mutations that cause germline feminization
Genetic interaction of mel-46 with fog-1, fem-3, and fog-2
Here we report the genetic isolation, molecular cloning and an initial phenotypic analysis of the gene mel-46. This gene encodes a protein of the DEAD box family and is required for embryogenesis, larval development and proper germline differentiation. Interestingly, also the mouse and the fly homologs of mel-46 were recently shown to be required for development and for proper function of the germ line. Mouillet et al. (2008)  demonstrated that murine DP103/Ddx20 is essential for early embryogenesis and influences ovarian morphology and function. Mutations in the Drosophila melanogaster Ddx20 ortholog, gemin3, lead to larval arrest and defects in the nurse cells in the germ line.
In C. elegans, the mutant phenotype of mel-46 is very reminiscent of the phenotype of ddx-23, a gene that also encodes a DEAD box protein. ddx-23 is homologous to human DDX23 and the yeast splicing factor PRP28. Analysis of mutants and RNAi knock down demonstrated that this gene is also required for embryonic viability, larval development and proper germline growth and differentiation, including the sperm-oocyte switch .
It is quite common that DEAD/H box proteins play multiple roles, both genetically and biochemically. A systematic RNAi analysis of genes that encode Helicase like proteins suggested that many DEAD/H box protein encoding genes are required multiple times during C. elegans development . Many proteins of this family possess RNA helicase activity and use ATP hydrolysis as an energy source to unwind RNA structures or separate RNA-protein complexes [24–26]. However, several members of this family are also involved in transcriptional regulation . For example the mammalian Ddx20/Gemin3/DP103 protein has been independently isolated as a transcriptional regulator of viral and nuclear genes (as Ddx20/DP103) [55–58], and as a component of the nuclear and cytoplasmic SMN complex (as Gemin3) , which plays roles in snRNP metabolism.
We describe two different mutant alleles of mel-46. The first one, yt5, is the reference allele and its molecular lesion is a premature stop codon towards the end of the penultimate exon. The second allele, tm1739, is a small deletion that takes out the entire exon 5 and would introduce a translational frame shift in the conserved DEAD box if exon 4 were spliced to exon 6. This mutation is therefore very likely to be a null. yt5 is temperature sensitive, and even at the restrictive temperature of 25°C, it is not null. The knockout allele tm1739 causes larval lethality that we did not observe in yt5 homozygous and yt5/tm1739 trans-heterozygous animals. Consistent with this idea, a truncated MEL-46 protein is present in mel-46(yt5) mutants (Fig 5) and might still perform some of the functions. The fact that yt5 is temperature sensitive and the yt5 mutant animals develop to adulthood allowed us to study the function of mel-46 in the germ line. However, we cannot completely exclude a neomorphic contribution to the phenotype that is caused by the truncated protein. However the yt5 mutation is fully recessive and mel-46 RNAi experiments lead to a fully penetrant Mel phenotype that was indistinguishable from that of yt5, indicating that yt5 is essentially a loss-of-function allele.
Germline defects in mel-46(yt5)
At 25°C mel-46(yt5) mutants display a range of germline defects. Some of the mel-46(yt5) adults produce embryos that undergo several rounds of cell division, indicating that these animals make functional gametes of both sexes. However, they have smaller broods than wild type animals demonstrating that their germ line is not entirely normal. Other hermaphrodites were defective in the proper formation of oocytes and did not produce any embryos. All animals did form normal looking sperm. In addition, mel-46(yt5) can partially suppress the complete self-sterility of the fog-2(q71) and fem-3(e2006) but not fog-1(q253). Although the suppression was weak it has to be taken into consideration that we were asking for suppression of feminizing mutations to the point that the double mutants produced functional sperm and functional oocytes. Being so rigorous it is very likely that we underestimate the masculinizing effect of mel-46(yt5). Our results are consistent with a genetic requirement of mel-46 for female germ cell differentiation downstream or in parallel of fog-2 and fem-3 and upstream of fog-1. However, although all mutant alleles used in this study are fully penetrant at 25°C, it has to be noticed that they are probably not null. For this reason and because the sex determining pathway is quite complex, the epistatic relationship of mel-46 with these three genes cannot be definitely determined with our assays. Although mel-46(yt5) clearly leads to a partial masculinization of the germ line, at the moment we do not know if this mutation affects sex determination specifically or if it also influences the function of other genes. The Mel-46 phenotype cannot be considered a classical Mog phenotype for various reasons. First, Mog animals produce large amounts of sperm (400 to 800 sperms per ovotestis ). We observed only a small fraction of animals with a slightly elevated sperm count and the average number of sperm was normal. Second, in the few mog mutants that occasionally produce limited amounts of oocytes when grown at permissive temperature, the spermatogenic region is distinct from that of oogenesis . This is different in mel-46(yt5) animals, as ooids were sometimes mixed with sperm. Third, when Mog animals are maintained to produce oocytes or ooids (for example in the case of a temperature downshift for mog-3(q74)), oocyte nuclei enter diakinesis with their chromosomes well separated (Fig 7G). In contrast in mel-46(yt5) mutants of class 1, only a small subset of ooids entered diakinesis. Moreover, such nuclei are significantly smaller as compared to those in mog-3(q74) animals (Fig 7F). Therefore, we suggest that the Mel-46 phenotype is primarily a defect in oocyte differentiation.
Here we report the genetic isolation, cloning and molecular and phenotypic characterization of the C. elegans gene mel-46. This gene encodes a putative DEAD box helicase and is required at least three times during development, namely: i) maternally for embryogenesis; ii) zygotically for progression through larval development and iii) in the hermaphrodite germ line. Consistent with these observations, we found the MEL-46 protein to be present at all developmental stages and in the germ line and in the soma. In this publication we focus on the requirement of mel-46 in the hermaphrodite germ line. We demonstrate that mel-46 weakly suppresses the feminizing mutations fog-2(q71) and fem-3(e2006) but not fog-1(q253). Although this genetic interaction indicates a certain feminizing activity of mel-46 in the germ line, we speculate that its primary function is in oocyte differentiation rather than sex determination.
Many of the C. elegans strains used in this study were obtained from the Caenorhabditis Genetics Center at University of Minnesota, which is funded by the National Institutes of Health. We would like to thank Dr Alex Hajnal for the lin-39::GFP and Dr Tibor Vellai for the nob-1::GFP reporters. The knock out alleles tm1739 and ok1475 were generated and sent to us by Dr Shohei Mitani (NBRP, Japan) and the International C. elegans Knockout Consortium respectively. We are grateful to the members of our laboratories and to Dr Ralf J. Sommer and the members of his laboratory for technical support and fruitful discussions, in particular we thank Metta Riebesell and Dr David Rudel for their help with gonad dissection and staining, Dr Werner Mayer for assistance with sequence analysis, Linda Nemetschke and Julia Vetter for technical assistance and Heike Haussmann for freezing strains. This work was supported by the Max Planck Society.
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