The hermaphrodite sperm/oocyte switch requires the Caenorhabditis elegans homologs of PRP2 and PRP22.

Proc Natl Acad Sci U S A

Department of Biochemistry and Howard Hughes Medical Institute, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.

Published: March 2000

Sex determination in the hermaphrodite germ line of Caenorhabditis elegans is controlled posttranscriptionally. The switch from spermatogenesis to oogenesis relies on regulation of the fem-3 sex-determining gene via a regulatory element in the fem-3 3' untranslated region. Previous work showed that at least six mog genes are required for repression by the fem-3 3' untranslated region, and that one of those genes, mog-1, encodes a DEAH-box protein. In this paper, we report the cloning of mog-4 and mog-5 and the finding that mog-4 and mog-5 also encode DEAH-box proteins. Our molecular identification of mog-4 and mog-5 relied on genetic mapping and transformation rescue and was confirmed by a missense mutation in each gene. A phylogenetic analysis revealed that the C. elegans MOG-1, MOG-4, and MOG-5 proteins are closely related to the yeast proteins PRP16, PRP2, and PRP22, respectively. In view of their effect on fem-3 regulation and their homology to PRP16, PRP2, and PRP22, we propose that MOG-1, MOG-4, and MOG-5 are required for posttranscriptional regulation, perhaps by modifying the conformation of ribonucleoprotein complexes.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC16229PMC
http://dx.doi.org/10.1073/pnas.97.7.3276DOI Listing

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Article Synopsis
  • - DDX-23, a DEAD-box protein in C. elegans, plays a critical role in RNA metabolism and is essential for both embryonic and post-embryonic development as well as somatic tissue differentiation.
  • - Inhibition of DDX-23 in the germline leads to reduced germ cell numbers and prevents the switch from making sperm to eggs (spermatogenesis to oogenesis).
  • - DDX-23 likely works alongside three other DEAH-box proteins (MOG-1, MOG-4, and MOG-5) in a shared pathway that impacts tissue differentiation, germline proliferation, and the sperm/egg switch through regulating ribonucleoprotein complexes.
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Cell fates in the Caenorhabditis elegans germline are regulated, at least in part, at the posttranscriptional level. For example, the switch from spermatogenesis to oogenesis in the hermaphrodite relies on posttranscriptional repression of the fem-3 mRNA via its 3' untranslated region (UTR). Previous studies identified three DEAH box proteins, MOG-1, MOG-4, and MOG-5, that are critical for the fem-3 3' UTR control.

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The hermaphrodite sperm/oocyte switch requires the Caenorhabditis elegans homologs of PRP2 and PRP22.

Proc Natl Acad Sci U S A

March 2000

Department of Biochemistry and Howard Hughes Medical Institute, University of Wisconsin, 433 Babcock Drive, Madison, WI 53706, USA.

Sex determination in the hermaphrodite germ line of Caenorhabditis elegans is controlled posttranscriptionally. The switch from spermatogenesis to oogenesis relies on regulation of the fem-3 sex-determining gene via a regulatory element in the fem-3 3' untranslated region. Previous work showed that at least six mog genes are required for repression by the fem-3 3' untranslated region, and that one of those genes, mog-1, encodes a DEAH-box protein.

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The Caenorhabditis elegans XX animal possesses a hermaphrodite germ line, producing first sperm, then oocytes. In this paper, we report the genetic identification of five genes, mog-2, mog-3, mog-4, mog-5, and mog-6, that influence the hermaphrodite switch from spermatogenesis to oogenesis. In mog-2-mog-6 mutants, spermatogenesis continues past the time at which hermaphrodites normally switch into oogenesis and no oocytes are observed.

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