Literature DB >> 19533027

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

Jiyoung Kim1, Ah-Reum Lee, Ichiro Kawasaki, Susan Strome, Yhong-Hee Shim.   

Abstract

By screening C. elegans mutants for severe defects in germline proliferation, we isolated a new loss-of-function allele of cdc-25.1, bn115. bn115 and another previously identified loss-of-function allele nr2036 do not exhibit noticeable cell division defects in the somatic tissues but have reduced numbers of germ cells and are sterile, indicating that cdc-25.1 functions predominantly in the germ line during postembryonic development, and that cdc-25.1 activity is probably not required in somatic lineages during larval development. We analyzed cell division of germ cells and somatic tissues in bn115 homozygotes with germline-specific anti-PGL-1 immunofluorescence and GFP transgenes that express in intestinal cells, in distal tip cells, and in gonadal sheath cells, respectively. We also analyzed the expression pattern of cdc-25.1 with conventional and quantitative RT-PCR. In the presence of three other family members of cdc-25 in C. elegans defects are observed only in the germ line but not in the somatic tissues in cdc-25.1 single mutants, and cdc-25.1 is expressed predominantly, if not exclusively, in the germ line during postembryonic stages. Our findings indicate that the function of cdc-25.1 is unique in the germ line but likely redundant with other members in the soma.

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Year:  2009        PMID: 19533027      PMCID: PMC2908335          DOI: 10.1007/s10059-009-0098-8

Source DB:  PubMed          Journal:  Mol Cells        ISSN: 1016-8478            Impact factor:   5.034


  23 in total

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Journal:  Dev Biol       Date:  1976-03       Impact factor: 3.582

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Authors:  Caroline Clucas; Juan Cabello; Ingo Büssing; Ralf Schnabel; Iain L Johnstone
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3.  CDC-25.1 regulates germline proliferation in Caenorhabditis elegans.

Authors:  Neville Ashcroft; Andy Golden
Journal:  Genesis       Date:  2002-05       Impact factor: 2.487

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Authors:  J E Sulston; H R Horvitz
Journal:  Dev Biol       Date:  1977-03       Impact factor: 3.582

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Authors:  G A Nelson; K K Lew; S Ward
Journal:  Dev Biol       Date:  1978-10       Impact factor: 3.582

6.  On the control of germ cell development in Caenorhabditis elegans.

Authors:  J E Kimble; J G White
Journal:  Dev Biol       Date:  1981-01-30       Impact factor: 3.582

7.  The postembryonic cell lineages of the hermaphrodite and male gonads in Caenorhabditis elegans.

Authors:  J Kimble; D Hirsh
Journal:  Dev Biol       Date:  1979-06       Impact factor: 3.582

8.  Genome-wide germline-enriched and sex-biased expression profiles in Caenorhabditis elegans.

Authors:  Valerie Reinke; Inigo San Gil; Samuel Ward; Keith Kazmer
Journal:  Development       Date:  2003-12-10       Impact factor: 6.868

9.  The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development.

Authors:  Ichiro Kawasaki; Anahita Amiri; Yuan Fan; Nicole Meyer; Steve Dunkelbarger; Tomoko Motohashi; Takeshi Karashima; Olaf Bossinger; Susan Strome
Journal:  Genetics       Date:  2004-06       Impact factor: 4.562

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Authors:  S Brenner
Journal:  Genetics       Date:  1974-05       Impact factor: 4.562

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Journal:  Genetics       Date:  2014-09-26       Impact factor: 4.562

6.  cdc-25.4, a Caenorhabditis elegans Ortholog of cdc25, Is Required for Male Mating Behavior.

Authors:  Sangmi Oh; Ichiro Kawasaki; Jae-Hyung Park; Yhong-Hee Shim
Journal:  G3 (Bethesda)       Date:  2016-12-07       Impact factor: 3.154

7.  Cell cycle controls stress response and longevity in C. elegans.

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8.  Neuronal GPCR NPR-8 regulates C. elegans defense against pathogen infection.

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  8 in total

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