Literature DB >> 2675488

Saccharomyces cerevisiae mutants defective in chromosome segregation.

J T McGrew1, Z X Xiao, M Fitzgerald-Hayes.   

Abstract

We have devised a genetic screen to identify trans-acting factors involved in chromosome transmission in yeast. This approach was designed to potentially identify a subset of genes encoding proteins that interact with centromere DNA. It has been shown that mutations in yeast centromere DNA cause aberrant chromosome segregation during mitosis and meiosis. We reasoned that the function of an altered centromere should be particularly sensitive to changes in factors with which it interacts. We constructed a disomic strain containing one copy of chromosome III with a wild-type centromere and one copy of chromosome III bearing the SUP11 gene and a mutant CEN3. This strain forms white colonies with red sectors due to nondisjunction of the chromosome bearing the mutant centromere. After mutagenesis we picked colonies that exhibited increased nondisjunction of the mutant chromosome as evidenced by increased red-white sectoring. Using this approach, we have isolated three trans-acting chromosome nondisjunction (cnd) mutants that are defective in maintaining chromosomes during mitosis in yeast.

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Year:  1989        PMID: 2675488     DOI: 10.1002/yea.320050407

Source DB:  PubMed          Journal:  Yeast        ISSN: 0749-503X            Impact factor:   3.239


  11 in total

1.  Analysis of centromere function in Saccharomyces cerevisiae using synthetic centromere mutants.

Authors:  M R Murphy; D M Fowlkes; M Fitzgerald-Hayes
Journal:  Chromosoma       Date:  1991-12       Impact factor: 4.316

2.  Suppressor analysis of a histone defect identifies a new function for the hda1 complex in chromosome segregation.

Authors:  Hasna Kanta; Lisa Laprade; Abeer Almutairi; Inés Pinto
Journal:  Genetics       Date:  2006-01-16       Impact factor: 4.562

3.  Analysis of primary structural determinants that distinguish the centromere-specific function of histone variant Cse4p from histone H3.

Authors:  K C Keith; R E Baker; Y Chen; K Harris; S Stoler; M Fitzgerald-Hayes
Journal:  Mol Cell Biol       Date:  1999-09       Impact factor: 4.272

4.  Histone H2A is required for normal centromere function in Saccharomyces cerevisiae.

Authors:  I Pinto; F Winston
Journal:  EMBO J       Date:  2000-04-03       Impact factor: 11.598

5.  Fission yeast mal2+ is required for chromosome segregation.

Authors:  U Fleig; M Sen-Gupta; J H Hegemann
Journal:  Mol Cell Biol       Date:  1996-11       Impact factor: 4.272

6.  CSE4 genetically interacts with the Saccharomyces cerevisiae centromere DNA elements CDE I and CDE II but not CDE III. Implications for the path of the centromere dna around a cse4p variant nucleosome.

Authors:  K C Keith; M Fitzgerald-Hayes
Journal:  Genetics       Date:  2000-11       Impact factor: 4.562

7.  CSE1 and CSE2, two new genes required for accurate mitotic chromosome segregation in Saccharomyces cerevisiae.

Authors:  Z Xiao; J T McGrew; A J Schroeder; M Fitzgerald-Hayes
Journal:  Mol Cell Biol       Date:  1993-08       Impact factor: 4.272

8.  A mutation in PLC1, a candidate phosphoinositide-specific phospholipase C gene from Saccharomyces cerevisiae, causes aberrant mitotic chromosome segregation.

Authors:  W E Payne; M Fitzgerald-Hayes
Journal:  Mol Cell Biol       Date:  1993-07       Impact factor: 4.272

9.  Isolation and characterization of Saccharomyces cerevisiae mutants defective in chromosome transmission in an undergraduate genetics research course.

Authors:  Heidi Major Sleister
Journal:  Genetics       Date:  2007-07-29       Impact factor: 4.562

10.  A tobacco etch virus protease with increased substrate tolerance at the P1' position.

Authors:  Christian Renicke; Roberta Spadaccini; Christof Taxis
Journal:  PLoS One       Date:  2013-06-24       Impact factor: 3.240

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