Literature DB >> 9705228

Genetic requirements for PIE-1 localization and inhibition of gene expression in the embryonic germ lineage of Caenorhabditis elegans.

C Tenenhaus1, C Schubert, G Seydoux.   

Abstract

In early Caenorhabditis elegans embryos, production of new mRNAs is inhibited in the germ lineage. This inhibition requires the germline factor PIE-1, and correlates with the absence in germline blastomeres of a phosphoepitope on RNA polymerase II (RNAPII-H5). We show that PIE-1 is uniformly distributed in oocytes and newly fertilized eggs, and becomes localized asymmetrically in the late one-cell stage. To begin to dissect the mechanisms required for PIE-1 localization and inhibition of RNAPII-H5 expression, we have examined the distribution of PIE-1 and RNAPII-H5 in maternal-effect mutants that disrupt embryonic development. We find that mutants that disrupt the asymmetric divisions of germline blastomeres mislocalize PIE-1, and activate RNAPII-H5 expression in the germ lineage. In contrast, mutants that alter somatic cell identities do not affect PIE-1 localization or RNAPII-H5 expression. Our observations suggest that PIE-1 represses mRNA transcription in each germline blastomere in a concentration-dependent manner. We also show that in wild-type, and in mutants where PIE-1 is mislocalized, the cellular and subcellular distribution of PIE-1 remarkably parallels that of the P granules, suggesting that the localizations of these two germline components are coordinately regulated. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9705228     DOI: 10.1006/dbio.1998.8940

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  39 in total

1.  Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases.

Authors:  Adrian A Cuenca; Aaron Schetter; Donato Aceto; Kenneth Kemphues; Geraldine Seydoux
Journal:  Development       Date:  2003-04       Impact factor: 6.868

2.  A conserved chromatin architecture marks and maintains the restricted germ cell lineage in worms and flies.

Authors:  Christine E Schaner; Girish Deshpande; Paul D Schedl; William G Kelly
Journal:  Dev Cell       Date:  2003-11       Impact factor: 12.270

3.  zif-1 translational repression defines a second, mutually exclusive OMA function in germline transcriptional repression.

Authors:  Tugba Guven-Ozkan; Scott M Robertson; Yuichi Nishi; Rueyling Lin
Journal:  Development       Date:  2010-09-08       Impact factor: 6.868

4.  Symmetry breaking and polarization of the C. elegans zygote by the polarity protein PAR-2.

Authors:  Seth Zonies; Fumio Motegi; Yingsong Hao; Geraldine Seydoux
Journal:  Development       Date:  2010-04-14       Impact factor: 6.868

5.  Transcription reactivation steps stimulated by oocyte maturation in C. elegans.

Authors:  Amy K Walker; Peter R Boag; T Keith Blackwell
Journal:  Dev Biol       Date:  2006-12-23       Impact factor: 3.582

6.  Inhibition of transcription by the Caenorhabditis elegans germline protein PIE-1: genetic evidence for distinct mechanisms targeting initiation and elongation.

Authors:  Dolan Ghosh; Geraldine Seydoux
Journal:  Genetics       Date:  2008-01       Impact factor: 4.562

7.  The kinases PIG-1 and PAR-1 act in redundant pathways to regulate asymmetric division in the EMS blastomere of C. elegans.

Authors:  Małgorzata J Liro; Diane G Morton; Lesilee S Rose
Journal:  Dev Biol       Date:  2018-09-10       Impact factor: 3.582

8.  The glucocorticoid receptor inhibits NFkappaB by interfering with serine-2 phosphorylation of the RNA polymerase II carboxy-terminal domain.

Authors:  R M Nissen; K R Yamamoto
Journal:  Genes Dev       Date:  2000-09-15       Impact factor: 11.361

9.  Alternative induction of meiotic recombination from single-base lesions of DNA deaminases.

Authors:  Siim Pauklin; Julia S Burkert; Julie Martin; Fekret Osman; Sandra Weller; Simon J Boulton; Matthew C Whitby; Svend K Petersen-Mahrt
Journal:  Genetics       Date:  2009-02-23       Impact factor: 4.562

10.  Global transcriptional repression in C. elegans germline precursors by regulated sequestration of TAF-4.

Authors:  Tugba Guven-Ozkan; Yuichi Nishi; Scott M Robertson; Rueyling Lin
Journal:  Cell       Date:  2008-10-03       Impact factor: 41.582

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