Literature DB >> 12361572

germ cell-less acts to repress transcription during the establishment of the Drosophila germ cell lineage.

Judith L Leatherman1, Lissa Levin, Julie Boero, Thomas A Jongens.   

Abstract

Previously, it has been shown that, during early Drosophila and C. elegans development, the germ cell precursors undergo a period of transcriptional quiescence. Here, we report that Germ cell-less (GCL), a germ plasm component necessary for the proper formation of "pole cells," the germ cell precursors in Drosophila, is required for the establishment of this transcriptional quiescence. While control embryos silence transcription prior to pole cell formation in the pole cell-destined nuclei, this silencing does not occur in embryos that lack GCL activity. The failure to establish quiescence is tightly correlated with failure to form the pole cells. Furthermore, we show that GCL can repress transcription of at least a subset of genes in an ectopic context, independent of other germ plasm components. Our results place GCL as the earliest gene known to act in the transcriptional repression of the germline. GCL's subcellular distribution on the nucleoplasmic surface of the nuclear envelope and its effect on transcription suggest that it may act to repress transcription in a manner similar to that proposed for transcriptional silencing of telomeric regions.

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Year:  2002        PMID: 12361572     DOI: 10.1016/s0960-9822(02)01182-x

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  27 in total

Review 1.  A germ-cell odyssey: fate, survival, migration, stem cells and differentiation. Meeting on germ cells.

Authors:  E Jane Albert Hubbard; Renee A Reijo Pera
Journal:  EMBO Rep       Date:  2003-03-21       Impact factor: 8.807

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.  The nuclear envelope at a glance.

Authors:  Katherine L Wilson; Jason M Berk
Journal:  J Cell Sci       Date:  2010-06-15       Impact factor: 5.285

4.  A conserved germline multipotency program.

Authors:  Celina E Juliano; S Zachary Swartz; Gary M Wessel
Journal:  Development       Date:  2010-12       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

Review 7.  Repression of somatic cell fate in the germline.

Authors:  Valérie J Robert; Steve Garvis; Francesca Palladino
Journal:  Cell Mol Life Sci       Date:  2015-06-05       Impact factor: 9.261

8.  Transcriptome profiles of Penaeus (Marsupenaeus) japonicus animal and vegetal half-embryos: identification of sex determination, germ line, mesoderm, and other developmental genes.

Authors:  Melony J Sellars; Carolyn Trewin; Sean M McWilliam; R S E Glaves; Philip L Hertzler
Journal:  Mar Biotechnol (NY)       Date:  2015-01-30       Impact factor: 3.619

9.  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

Review 10.  The development of germline stem cells in Drosophila.

Authors:  David A Dansereau; Paul Lasko
Journal:  Methods Mol Biol       Date:  2008
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