Literature DB >> 9043088

The C. elegans MEX-1 protein is present in germline blastomeres and is a P granule component.

S Guedes1, J R Priess.   

Abstract

In the nematode Caenorhabditis elegans, germ cells arise from early embryonic cells called germline blastomeres. Cytoplasmic structures called P granules are present in the fertilized egg and are segregated into each of the germline blastomeres during the first few cleavages of the embryo. Mutations in the maternally expressed gene mex-1 disrupt the segregation of P granules, prevent the formation of germ cells, and cause inappropriate patterns of somatic cell differentiation. We have cloned the mex-1 gene and determined the distribution pattern of the mex-1 gene products. The MEX-1 protein contains two copies of an unusual 'finger' domain also found in the PIE-1 protein of C. elegans. PIE-1 has been shown to be expressed in germline blastomeres, and is a component of P granules. We show here that MEX-1 also is present in germline blastomeres and is a P granule component, although MEX-1 is a cytoplasmic protein while PIE-1 is present in both the nucleus and cytoplasm. We further show that MEX-1 is required to restrict PIE-1 expression and activity to the germline blastomeres during the early embryonic cleavages.

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Year:  1997        PMID: 9043088     DOI: 10.1242/dev.124.3.731

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  36 in total

1.  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

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

Review 3.  New insights into the regulation of RNP granule assembly in oocytes.

Authors:  Jennifer A Schisa
Journal:  Int Rev Cell Mol Biol       Date:  2012       Impact factor: 6.813

4.  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

5.  Use of cDNA subtraction and RNA interference screens in combination reveals genes required for germ-line development in Caenorhabditis elegans.

Authors:  M Hanazawa; M Mochii; N Ueno; Y Kohara; Y Iino
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

6.  Regulation of maternal Wnt mRNA translation in C. elegans embryos.

Authors:  Marieke Oldenbroek; Scott M Robertson; Tugba Guven-Ozkan; Caroline Spike; David Greenstein; Rueyling Lin
Journal:  Development       Date:  2013-10-16       Impact factor: 6.868

7.  RNA recognition by the Caenorhabditis elegans oocyte maturation determinant OMA-1.

Authors:  Ebru Kaymak; Sean P Ryder
Journal:  J Biol Chem       Date:  2013-09-06       Impact factor: 5.157

Review 8.  P granule assembly and function in Caenorhabditis elegans germ cells.

Authors:  Dustin Updike; Susan Strome
Journal:  J Androl       Date:  2009-10-29

Review 9.  Germ cell specification.

Authors:  Jennifer T Wang; Geraldine Seydoux
Journal:  Adv Exp Med Biol       Date:  2013       Impact factor: 2.622

Review 10.  Asymmetric cell divisions in the epidermis.

Authors:  Nicholas D Poulson; Terry Lechler
Journal:  Int Rev Cell Mol Biol       Date:  2012       Impact factor: 6.813

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