Literature DB >> 2680756

Pachytene arrest and other meiotic effects of the start mutations in Saccharomyces cerevisiae.

E O Shuster1, B Byers.   

Abstract

Mutations in the Start class of cell division cycle genes (CDC28, CDC36 and CDC39) define the point in the G1 phase of the vegetative cycle at which the cell becomes committed to completing another round of cell division. Genetic, cytological and biochemical data demonstrate that these mutations cause meiotic cells to become arrested at pachytene following completion of both chromosomal DNA replication and spindle pole body (SPB) duplication. In contrast these mutations have previously been found to cause arrest of the mitotic cell cycle prior to either of these landmark events, so the role of the Start genes in these events during vegetative growth must be indirect. Our observations are consistent with the hypothesis that CDC28, CDC36 and CDC39 are required for irreversible commitment to nuclear division in both the mitotic and meiotic pathways. CDC28 was additionally found to be required for the SPB separation that precedes spindle formation in preparation for the second meiotic division. Cytological and genetic analyses of this requirement revealed both that such separation may fail independently at either SPB and that ascospore formation can proceed independently of SPB separation.

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Year:  1989        PMID: 2680756      PMCID: PMC1203788     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  54 in total

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Journal:  Genetics       Date:  1980-07       Impact factor: 4.562

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Journal:  Nature       Date:  1988-06-16       Impact factor: 49.962

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Journal:  Chromosoma       Date:  1979-10-02       Impact factor: 4.316

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Journal:  Nature       Date:  1982-12-23       Impact factor: 49.962

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Authors:  R E Esposito; M S Esposito
Journal:  Proc Natl Acad Sci U S A       Date:  1974-08       Impact factor: 11.205

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  74 in total

1.  The Saccharomyces cerevisiae centromere protein Slk19p is required for two successive divisions during meiosis.

Authors:  X Zeng; W S Saunders
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

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Authors:  Kirsten R Benjamin; Chao Zhang; Kevan M Shokat; Ira Herskowitz
Journal:  Genes Dev       Date:  2003-06-03       Impact factor: 11.361

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Authors:  V Parkes; L H Johnston
Journal:  Nucleic Acids Res       Date:  1992-11-11       Impact factor: 16.971

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Authors:  R A Sclafani; T M Holzen
Journal:  Annu Rev Genet       Date:  2007       Impact factor: 16.830

5.  Ovol1 regulates meiotic pachytene progression during spermatogenesis by repressing Id2 expression.

Authors:  Baoan Li; Mahalakshmi Nair; Douglas R Mackay; Virginia Bilanchone; Ming Hu; Magid Fallahi; Hanqiu Song; Qian Dai; Paula E Cohen; Xing Dai
Journal:  Development       Date:  2005-02-16       Impact factor: 6.868

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Authors:  G S Roeder
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-07       Impact factor: 11.205

7.  The Ama1-directed anaphase-promoting complex regulates the Smk1 mitogen-activated protein kinase during meiosis in yeast.

Authors:  Christine M McDonald; Katrina F Cooper; Edward Winter
Journal:  Genetics       Date:  2005-08-03       Impact factor: 4.562

8.  Phosphorylation and maximal activity of Saccharomyces cerevisiae meiosis-specific transcription factor Ndt80 is dependent on Ime2.

Authors:  Richelle Sopko; Sheetal Raithatha; David Stuart
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

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Authors:  D X Tishkoff; A W Johnson; R D Kolodner
Journal:  Mol Cell Biol       Date:  1991-05       Impact factor: 4.272

10.  Nutritional regulation of late meiotic events in Saccharomyces cerevisiae through a pathway distinct from initiation.

Authors:  R H Lee; S M Honigberg
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

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