Caenorhabditis elegans gene dpy-21, DumPY : shorter than wild-type, encoding round spermatid basic protein 1-like CRA a.
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SUMMARY

Summary
[Wormbase] dpy-21 encodes a novel, conserved protein with a proline-rich N terminus; dpy-21 affects RNA levels of X-linked dosage-compensated genes, body length in hermaphrodites, and fertility and male tail development in males; DPY-21 interacts in vivo with DPY-27 and SDC-3, members of the dosage compensation complex, and like members of the dosage compensation complex, is diffusely localized in nuclei of XX embryos containing <40 cells, but then specifically localizes to X chromosomes of XX embryos with >40 cells, remaining on the X throughout development; in XO embryos, DPY-21 is dispersed throughout the nucleus in multiple foci that are not coincident with the X chromosome; in hermaphrodites, localization of DPY-21 to the X chromosome requires activity of SDC-2, SDC-3, DPY-26, DPY-27, and DPY-28; DPY-21 is not, however, required reciprocally for the stability or localization of these other dosage compensation proteins; in addition, unlike SDC-3 and other members of the dosage compensation complex, DPY-21 is not recruited to the autosomal her-1 regulatory region, suggesting that DPY-21 is not part of the gene-specific complex that represses her-1 expression in hermaphrodites
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Wormbase predicts one model from 2 genes, but Caenorhabditis elegans cDNA sequences in GenBank, filtered against clone rearrangements, coaligned on the genome and clustered in a minimal non-redundant way by the manually supervised AceView program, support at least 2 spliced variants.
AceView summary
Expression: According to AceView, this gene is
well expressed, 1.2 times the average gene in this release, at all stages of development [Kohara cDNAs]. The
sequence of this gene is defined by
16 cDNA clones. We annotate
structural defects or features in 2 cDNA clones.
Alternative mRNA variants and regulation: The gene contains
11 distinct gt-ag introns. Transcription produces
2 alternatively spliced mRNAs. The mRNAs appear to differ by by presence or absence of a
cassette exon.
Protein coding potential: The 2 spliced mRNAs putatively encode
good proteins, altogether
2 different isoforms (2 complete, 1 COOH complete), some containing a coiled coil stretch
[Psort2].
Function: There are
9 articles specifically referring to this gene in PubMed. In addition we point
below to 47 abstracts. This gene is associated to a
phenotype (DumPY : shorter than wild-type). Proteins are expected to
localize in nucleus.
Please quote:
AceView: a comprehensive cDNA-supported gene and transcripts annotation, Genome Biology 2006, 7(Suppl 1):S12
Map on chromosome CHROMOSOME_V, links to other databases and other names
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Map: This gene dpy-21 maps on chomosome V at position +13.19 (interpolated). In AceView, it covers
12.89 kb, from 17949149 to 17936262 (WS190), on the reverse strand.
Links to: WormBase,
NextDB,
RNAiDB.
Other names: The gene is also known in Wormgenes/AceView by its positional name 5S418, in Wormbase by its cosmid.number name Y59A8B.1, in NextDB, the Nematode expression pattern database, as CEYK3009.
Closest AceView homologs in other species
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The closest human genes, according to BlastP, are the AceView genes
RSBN1L (e=9 10^-74),
RSBN1 (e=9 10^-74).
The closest mouse genes, according to BlastP, are the AceView genes
Rsbn1l (e=3 10^-74),
Rsbn1andPhtf1 (e=3 10^-72)
Complete gene on genome diagram: (in true scale, with colored introns)

This diagram was in previous releases displayed by default on the right of the screen. It shows in true scale the gene on the genome, the mRNAs and the cDNA clones. Opening may be slow for large genes. Please choose between the
zoomable GIF version., and the
Flash version
Compact gene diagram

Alternative mRNAs are shown aligned from 5' to 3' on a virtual genome where
introns have been shrunk to a minimal length. Exon size is proportional to length,
intron height reflects the number of cDNA clones supporting each intron. Superimposed introns of the same color are identical, of different colors are different.
Mouse over the ending of each transcript gives tissues from which the supporting cDNAs were extracted. Click on any transcript to open the specific mRNA page, to see the exact cDNA clone support and eventual SNPs and to get details on tissues, sequences, mRNA and protein annotations. Details on tissue of origin for each intron and exon is available from the
intron and exons table. Good predicted proteins are in pink, yellow proteins may be partial or unconvincing, green are uORFs. Proteins supported by a single continuous GenBank accession lead to underlining the name/ending of the variant. Names not underlined result from cDNA concatenation in the coding region and should be experimentally checked.
More legend
Introns are depicted by broken lines; the height of the top of each intron reflects the relative number of clones supporting this intron.
]^[ A pink broken line denotes an intron with standard boundaries (gt-ag or gc-ag) that is exactly supported (i.e. a cDNA sequence exactly matches the genome over 16 bp, 8 on both sides of the intron).
] ^ ] A blue broken line denotes non-standard introns, exactly supported, but with non-standard at-ac or any other boundaries.
]-[ Pink and
] - ] blue straight lines represent 'fuzzy' introns of the standard and non-standard types respectively, those introns do not follow the 16 bp rule. Black straight lines ]-[denote gaps in the alignments.
Exons: Wide filled pink areas represent putative protein coding regions, narrow empty pink boxes represent the 5'UTR (on the left) and 3' UTR (on the right). Flags identify validated endings: cap site on the 5' side, polyadenylation site on the 3' side. Filled flags correspond to frequent events while empty flags have lesser supporting cDNAs (yet all are validated); at the 3' side, black flags are associated to the main AATAAA signal,
blue flags to any single letter variant of the main . More explanations are given in the
gene help file
Sequences

What is known about the gene and its neighbors on chromosome CHROMOSOME_V

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D:disease,
C:conserved,
I:interactions,
R:regulation,
P:publications (see the
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D:disease,
C:conserved,
I:interactions,
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Annotated mRNA diagrams

The mRNAs diagrams with the aligned cDNA sequence accessions and their mismatches are available in the mRNA pages accessible from the tab at the top of the page, or here:
In Flash:
.a, .b.
or in GIF:
.a, .b
Bibliography

Please see these
10 articles in PubMed.
In addition we found 47 papers for which we do not have a PubMed identifier
- [wbg3.1p17] further studies with the X-linked lethals.
- [wbg3.2p19b]
- [wbg7.2p24] two notes on sex discrimination.
- [wbg7.2p48] identification of a dominant transformer allele of her-1.
- [wbg7.1p80] studies with dpy-21.
- [wbg7.2p11] somatic damage to the X chromosome of C elegans induced by gamma radiation.
- [wbg7.2p15] autosomal genes affected by X-chromosome dose.
- [wbg8.1p6] genetics of X-chromosome expression.
- [wbg8.1p5] developmental regulation of DNA repair in C elegans.
- [wbg8.3p68] mapping a 5S DNA cluster.
- [wbg8.2p7] genes regulating X-chromosome expression.
- [wbg8.3p37] more about sex-linked gene expression.
- [wbg8.3p38] dosage compensation operates at the level of transcription in C elegans.
- [wbg9.1p73] molecular analysis of dosage compensation continues.
- [wbg9.1p74] X chromosome expression in X duplications and in some new mutations.
- [wbg9.1p75] further steps towards a genetic understanding of dosage compensation.
- [wbg9.1p77] more about dosage compensation.
- [wbg9.1p78] egl-16: a gene which unites the sex determination and dosage compensation pathways.
- [wbg9.2p92] a maternal-effect mutation that results in XO-specific lethality.
- [wbg9.2p91] effects of duplicating X-linked genes on the general expression of the Xchromosome.
- [wbg9.2p89] sleeping worms don't lie.
- [wbg9.2p70] screens for maternal-effect lethal mutations affecting the gut lineage.
- [wbg9.3p49] more about X-linked gene expression in X-duplication and X-dependent Dpy strains.
- [wbg10.1p79] an autosomal X-linked duplication.
- [wbg10.1p131] xol-1: a gene essential for male viability is involved in both sex determination and dosage compensation.
- [wbg10.3p19] searching for XX-XO mosaics.
- [wbg10.2p18] more about xol-1: a gene that controls the male mode of sex determination and dosage compensation.
- [wbg10.2p23] dpy-29: yet another XX-specific lethal.
- [wbg10.3p8] spy-29 and tra V: Jekyll and Hyde ?
- [wbg10.3p10] stalking the dpy-21 null phenotype.
- [wbg11.4p92] A zygotic embryonic lethal mutant defective in specifying multiple embryonic cell fates, gastrulation, and cell adhesion
- [wbg11.3p51] Mutations in the sex determination function of dpy-29 cause inappropriate overexpression of her-1 transcripts in XX animals.
- [wbg11.3p53] Mapping of Fluoride-resistant Mutants
- [wbg11.4p20] unc-80 IS A STUPID GENE
- [wbg13.1p60] Is Differential Histone H4 Acetylation Involved in the Mechanism of DosageCompensation?
- [wbg13.3p39] DPY-27: A Protein Required For Dosage Compensation is Associated With the X Chromosome in XX Animals
- [wbg13.3p38] Evidence For Interactions Between the Sex Determination and Dosage Compensation Pathways in the Germline
- [wbg13.5p66] SL1 Performs An Essential Function In Early Embryogenesis.
- [wbg14.1p27] DPY-26 is a Novel Protein Associated with the X Chromosomes in XX Animals
- [wbg14.1p50] Cell and Axon Migrations are Misdirected in dpy-23 Mutants
- [wm95p163] CLONING THE DOSAGE COMPENSATION GENE dpy-21.
- [wm95p491] CAENORHABDITIS ELEGANS: BALANCERS, RECESSIVE LETHAL MUTATIONS AND DEFICIENCIES ON LGIII(LEFT) AND LGV(RIGHT).
- [wcwm96p93] Cloning the dosage compensation gene, dpy-21
- [wm97ab99] Cloning the dosage compensation gene, dpy-21
- [wcwm98p62] dpy-28: AN ESSENTIAL DOSAGE COMPENSATION GENE ALSO REQUIRED FOR MEIOTIC CHROMOSOME SEGREGATION ENCODES A CHROMOSOME CONDENSATION HOMOLOG
- [wcwm2000p259] Molecular Analysis of the Dosage Compensation Gene dpy-21
- [wm2001p768] Molecular Characterization of the Dosage Compensation Gene, dpy-21
To mine knowledge about the gene, please click the 'Gene Summary' or the 'Function and related genes' tab at the top of the page. The 'Gene Summary' page includes all we learnt about the gene, functional annotations of neighboring genes, maps, links to other sites and the bibliography. The 'Function and related genes' page includes Diseases (D), Pathways, GO annotations, conserved domains (C), interactions (I) reference into function, and pointers to all genes with the same functional annotation.
To compare all variants, their summarized annotations, introns and exons, or to access any sequence, click the 'Alternative mRNAs features' tab. To see a specific mRNA variant diagram, sequence and annotation, click the variant name in the 'mRNA' tab. To examine expression data from all cDNAs clustered in this gene by AceView, click the 'Expression tissue'.
If you know more about this gene, or found errors, please share your knowledge. Merci !