Literature DB >> 12001064

CDC-25.1 regulates germline proliferation in Caenorhabditis elegans.

Neville Ashcroft1, Andy Golden.   

Abstract

The cell cycles in C. elegans are tightly controlled but appear to use the same regulators found in other organisms. Four homologues of the dual-specificity phosphatase Cdc25 are present in the C. elegans genome. In our study, we have characterized a deletion mutant for one of these orthologues. We show that embryonic defects are absent in cdc-25.1 homozygous mutants, presumably because of maternally contributed CDC-25.1 product. These embryos hatch and develop into sterile adults. The adults do not appear to have any somatic defects. The sterility results from inadequate germline proliferation. Germline precursors divide slowly and produce abnormally sized daughter cells. Only three to four rounds of germ-cell division occur before they die during the L3 and L4 larval stages. Copyright 2002 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12001064     DOI: 10.1002/gene.10083

Source DB:  PubMed          Journal:  Genesis        ISSN: 1526-954X            Impact factor:   2.487


  19 in total

1.  mir-35 is involved in intestine cell G1/S transition and germ cell proliferation in C. elegans.

Authors:  Min Liu; Pengpeng Liu; Li Zhang; Qingchun Cai; Ge Gao; Wenxia Zhang; Zuoyan Zhu; Dong Liu; Qichang Fan
Journal:  Cell Res       Date:  2011-06-21       Impact factor: 25.617

2.  CDC-25.2, a C. elegans ortholog of cdc25, is essential for the progression of intestinal divisions.

Authors:  Yong-Uk Lee; Miseol Son; Jiyoung Kim; Yhong-Hee Shim; Ichiro Kawasaki
Journal:  Cell Cycle       Date:  2016       Impact factor: 4.534

Review 3.  Developmental Control of the Cell Cycle: Insights from Caenorhabditis elegans.

Authors:  Edward T Kipreos; Sander van den Heuvel
Journal:  Genetics       Date:  2019-03       Impact factor: 4.562

Review 4.  In vivo roles of CDC25 phosphatases: biological insight into the anti-cancer therapeutic targets.

Authors:  Hiroaki Kiyokawa; Dipankar Ray
Journal:  Anticancer Agents Med Chem       Date:  2008-12       Impact factor: 2.505

5.  Down-regulation of tricarboxylic acid (TCA) cycle genes blocks progression through the first mitotic division in Caenorhabditis elegans embryos.

Authors:  Mohammad M Rahman; Simona Rosu; Daphna Joseph-Strauss; Orna Cohen-Fix
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-03       Impact factor: 11.205

6.  Burkholderia pseudomallei kills Caenorhabditis elegans through virulence mechanisms distinct from intestinal lumen colonization.

Authors:  Soon-Keat Ooi; Tian-Yeh Lim; Song-Hua Lee; Sheila Nathan
Journal:  Virulence       Date:  2012-10-01       Impact factor: 5.882

7.  A mutation of cdc-25.1 causes defects in germ cells but not in somatic tissues in C. elegans.

Authors:  Jiyoung Kim; Ah-Reum Lee; Ichiro Kawasaki; Susan Strome; Yhong-Hee Shim
Journal:  Mol Cells       Date:  2009-06-12       Impact factor: 5.034

8.  Virulence of Leucobacter chromiireducens subsp. solipictus to Caenorhabditis elegans: characterization of a novel host-pathogen interaction.

Authors:  Rachel E Muir; Man-Wah Tan
Journal:  Appl Environ Microbiol       Date:  2008-05-16       Impact factor: 4.792

9.  C. elegans RNA-binding proteins PUF-8 and MEX-3 function redundantly to promote germline stem cell mitosis.

Authors:  Mohd Ariz; Rana Mainpal; Kuppuswamy Subramaniam
Journal:  Dev Biol       Date:  2008-12-07       Impact factor: 3.582

10.  Fate specification and tissue-specific cell cycle control of the Caenorhabditis elegans intestine.

Authors:  Alexandra Segref; Juan Cabello; Caroline Clucas; Ralf Schnabel; Iain L Johnstone
Journal:  Mol Biol Cell       Date:  2010-01-06       Impact factor: 4.138

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.