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

Molecular and Cellular Biology 31 巻 3 号 495-506 頁 2011-02 発行
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タイトル ( eng )
Fission Yeast Pot1 and RecQ Helicase Are Required for Efficient Chromosome Segregation
作成者
Takahashi Katsunori
Imano Ryota
Kibe Tatsuya
Seimiya Hiroyuki
Muramatsu Yukiko
Kawabata Naoki
Tanaka Genki
Matsumoto Yoshitake
Hiromoto Taisuke
Koizumi Yuka
Nakazawa Norihiko
Yanagida Mitsuhiro
収録物名
Molecular and Cellular Biology
31
3
開始ページ 495
終了ページ 506
抄録
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.
著者キーワード
Telomere
Pot1
RecQ helicase
Anti-microtubule drug
NDC分類
生物科学・一般生物学 [ 460 ]
言語
英語
資源タイプ 学術雑誌論文
出版者
American Society for Microbiology
発行日 2011-02
権利情報
Copyright (c) American Society for Microbiology, Mol. Cell. Biol. February 2011 vol. 31 no. 3 495-506, doi: 10.1128/MCB.00613-10
出版タイプ Author’s Original(十分な品質であるとして、著者から正式な査読に提出される版)
アクセス権 オープンアクセス
収録物識別子
[ISSN] 0270-7306
[DOI] 10.1128/MCB.00613-10
[NCID] AA10620925
[DOI] http://dx.doi.org/10.1128/MCB.00613-10