Literature DB >> 8751440

The PIE-1 protein and germline specification in C. elegans embryos.

C C Mello1, C Schubert, B Draper, W Zhang, R Lobel, J R Priess.   

Abstract

Totipotent germline blastomeres in Caenorhabditis elegans contain, but do not respond to, factors that promote somatic differentiation in other embryonic cells. Mutations in the maternal gene pie-1 result in the germline blastomeres adopting somatic cell fates. Here we show that pie-1 encodes a nuclear protein, PIE-1, that is localized to the germline blastomeres throughout early development. During division of each germline blastomere, PIE-1 initially associates with both centrosomes of the mitotic spindle. However, PIE-1 rapidly disappears from the centrosome destined for the somatic daughter, and persists in the centrosome of the daughter that becomes the next germline blastomere. The PIE-1 protein contains potential zinc-finger motifs also found in the mammalian growth-factor response protein TIS-11/NUP475 (refs 4-7). The localization and genetic properties of pie-1 provide an example of a repressor-based mechanism for preserving pluripotency within a stem cell lineage.

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Year:  1996        PMID: 8751440     DOI: 10.1038/382710a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  97 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.  Arginine-rich regions mediate the RNA binding and regulatory activities of the protein encoded by the Drosophila melanogaster suppressor of sable gene.

Authors:  M A Turnage; P Brewer-Jensen; W L Bai; L L Searles
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

3.  Distinct requirements for somatic and germline expression of a generally expressed Caernorhabditis elegans gene.

Authors:  W G Kelly; S Xu; M K Montgomery; A Fire
Journal:  Genetics       Date:  1997-05       Impact factor: 4.562

4.  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

5.  RNA in centrosomes: structure and possible functions.

Authors:  Konstantin Chichinadze; Ann Lazarashvili; Jaba Tkemaladze
Journal:  Protoplasma       Date:  2012-06-10       Impact factor: 3.356

6.  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

7.  Nucleoporins NPP-1, NPP-3, NPP-4, NPP-11 and NPP-13 are required for proper spindle orientation in C. elegans.

Authors:  Aaron Schetter; Peter Askjaer; Fabio Piano; Iain Mattaj; Kenneth Kemphues
Journal:  Dev Biol       Date:  2005-12-02       Impact factor: 3.582

8.  Suppressor of sable, a putative RNA-processing protein, functions at the level of transcription.

Authors:  Yung-Shu Kuan; Paul Brewer-Jensen; Lillie L Searles
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

9.  RNA target specificity of the embryonic cell fate determinant POS-1.

Authors:  Brian M Farley; John M Pagano; Sean P Ryder
Journal:  RNA       Date:  2008-10-24       Impact factor: 4.942

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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