Literature DB >> 9339342

The mcm17 mutation of yeast shows a size-dependent segregational defect of a mini-chromosome.

N Roy1, A Poddar, A Lohia, P Sinha.   

Abstract

Mini-chromosome-maintenance (mcm) mutants were described earlier as yeast mutants which could not stably maintain mini-chromosomes. Out of these, the ARS-specific class has been more extensively studied and is found to lose chromosomes and mini-chromosomes due to a defect in the initiation of DNA replication at yeast ARSs. In the present study we have identified a number of mcm mutants which show size-dependent loss of mini-chromosomes. When the size of the mini-chromosome was increased, from about 15 kb to about 60 kb, there was a dramatic increase in its mitotic stability in these mutants, but not in the ARS-specific class of mutants. One mutant, mcm17, belonging to the size-dependent class was further characterized. In this mutant, cells carried mini-chromosomes in significantly elevated copy numbers, suggesting a defect in segregation. This defect was largely suppressed in the 60-kb mini-chromosome. A non-centromeric plasmid, the TRP1ARS1 circle, was not affected in its maintenance. This mutant also displayed enhanced chromosome-III loss during mitosis over the wild-type strain, without elevating mitotic recombination. Cloning and sequencing of MCM17 has shown it to be the same as CHL4, a gene required for chromosome stability. This gene is non-essential for growth, as its disruption or deletion from the chromosome did not affect the growth-rate of cells at 23 degrees C or 37 degrees C. This work suggests that centromere-directed segregation of a chromosome in yeast is strongly influenced by its length.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9339342     DOI: 10.1007/s002940050264

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   3.886


  13 in total

Review 1.  The Mcm complex: unwinding the mechanism of a replicative helicase.

Authors:  Matthew L Bochman; Anthony Schwacha
Journal:  Microbiol Mol Biol Rev       Date:  2009-12       Impact factor: 11.056

2.  Ctf3p, the Mis6 budding yeast homolog, interacts with Mcm22p and Mcm16p at the yeast outer kinetochore.

Authors:  Vivien Measday; Dale W Hailey; Isabelle Pot; Scott A Givan; Katherine M Hyland; Gerard Cagney; Stan Fields; Trisha N Davis; Philip Hieter
Journal:  Genes Dev       Date:  2002-01-01       Impact factor: 11.361

Review 3.  Diversity in requirement of genetic and epigenetic factors for centromere function in fungi.

Authors:  Babhrubahan Roy; Kaustuv Sanyal
Journal:  Eukaryot Cell       Date:  2011-09-09

4.  Chl4p and iml3p are two new members of the budding yeast outer kinetochore.

Authors:  Isabelle Pot; Vivien Measday; Brian Snydsman; Gerard Cagney; Stanley Fields; Trisha N Davis; Eric G D Muller; Philip Hieter
Journal:  Mol Biol Cell       Date:  2003-02       Impact factor: 4.138

5.  The Iml3 protein of the budding yeast is required for the prevention of precocious sister chromatid separation in meiosis I and for sister chromatid disjunction in meiosis II.

Authors:  Santanu Kumar Ghosh; Soumitra Sau; Sudeshna Lahiri; Anuradha Lohia; Pratima Sinha
Journal:  Curr Genet       Date:  2004-07-06       Impact factor: 3.886

6.  Sequential MCM/P1 subcomplex assembly is required to form a heterohexamer with replication licensing activity.

Authors:  T A Prokhorova; J J Blow
Journal:  J Biol Chem       Date:  2000-01-28       Impact factor: 5.157

7.  Implication of a novel multiprotein Dam1p complex in outer kinetochore function.

Authors:  I M Cheeseman; C Brew; M Wolyniak; A Desai; S Anderson; N Muster; J R Yates; T C Huffaker; D G Drubin; G Barnes
Journal:  J Cell Biol       Date:  2001-12-24       Impact factor: 10.539

8.  The budding yeast protein Chl1p is required to preserve genome integrity upon DNA damage in S-phase.

Authors:  Suparna Laha; Shankar Prasad Das; Sujata Hajra; Soumitra Sau; Pratima Sinha
Journal:  Nucleic Acids Res       Date:  2006-10-24       Impact factor: 16.971

9.  Establishment of cohesion at the pericentromere by the Ctf19 kinetochore subcomplex and the replication fork-associated factor, Csm3.

Authors:  Josefin Fernius; Adele L Marston
Journal:  PLoS Genet       Date:  2009-09-04       Impact factor: 5.917

10.  Differential kinetochore protein requirements for establishment versus propagation of centromere activity in Saccharomyces cerevisiae.

Authors:  Karthikeyan Mythreye; Kerry S Bloom
Journal:  J Cell Biol       Date:  2003-03-17       Impact factor: 10.539

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.