Fission Yeast Pot1 and RecQ Helicase Are Required for Efficient Chromosome Segregation

Molecular and Cellular Biology Volume 31 Issue 3 Page 495-506 published_at 2011-02
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Title ( eng )
Fission Yeast Pot1 and RecQ Helicase Are Required for Efficient Chromosome Segregation
Creator
Takahashi Katsunori
Imano Ryota
Kibe Tatsuya
Seimiya Hiroyuki
Muramatsu Yukiko
Kawabata Naoki
Tanaka Genki
Matsumoto Yoshitake
Hiromoto Taisuke
Koizumi Yuka
Nakazawa Norihiko
Yanagida Mitsuhiro
Source Title
Molecular and Cellular Biology
Volume 31
Issue 3
Start Page 495
End Page 506
Abstract
Pot1 is a single-stranded telomere-binding protein that is conserved from fission yeast to mammals. Deletion of Schizosaccharomyces pombe pot1+ causes immediate telomere loss. S. pombe Rqh1 is a homolog of the human RecQ helicase WRN, which plays essential roles in the maintenance of genomic stability. Here, we demonstrate that a pot1Δ rqh1-hd (helicase-dead) double mutant maintains telomeres that are dependent on Rad51-mediated homologous recombination. Interestingly, the pot1Δ rqh1-hd double mutant displays a “cut" (cell untimely torn) phenotype and is sensitive to the antimicrotubule drug thiabendazole (TBZ). Moreover, the chromosome ends of the double mutant do not enter the pulsed-field electrophoresis gel. These results suggest that the entangled chromosome ends in the pot1Δ rqh1-hd double mutant inhibit chromosome segregation, signifying that Pot1 and Rqh1 are required for efficient chromosome segregation. We also found that POT1 knockdown, WRN-deficient human cells are sensitive to the antimicrotubule drug vinblastine, implying that some of the functions of S. pombe Pot1 and Rqh1 may be conserved in their respective human counterparts POT1 and WRN.
Keywords
Telomere
Pot1
RecQ helicase
Anti-microtubule drug
NDC
Biology [ 460 ]
Language
eng
Resource Type journal article
Publisher
American Society for Microbiology
Date of Issued 2011-02
Rights
Copyright (c) American Society for Microbiology, Mol. Cell. Biol. February 2011 vol. 31 no. 3 495-506, doi: 10.1128/MCB.00613-10
Publish Type Author’s Original
Access Rights open access
Source Identifier
[ISSN] 0270-7306
[DOI] 10.1128/MCB.00613-10
[NCID] AA10620925
[DOI] http://dx.doi.org/10.1128/MCB.00613-10