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Two XMAP215/TOG Microtubule Polymerases, Alp14 and Dis1, Play Non-Exchangeable, Distinct Roles in Microtubule Organisation in Fission Yeast

https://hiroshima.repo.nii.ac.jp/records/2007120
https://hiroshima.repo.nii.ac.jp/records/2007120
a615c1d2-201c-49d7-8ab8-b5e24b44eff3
名前 / ファイル ライセンス アクション
IJMS_20_5108.pdf IJMS_20_5108.pdf (3.6 MB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル Two XMAP215/TOG Microtubule Polymerases, Alp14 and Dis1, Play Non-Exchangeable, Distinct Roles in Microtubule Organisation in Fission Yeast
言語 en
作成者 Yukawa, Masashi

× Yukawa, Masashi

en Yukawa, Masashi

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Kawakami, Tomoki

× Kawakami, Tomoki

en Kawakami, Tomoki

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Pinder, Corinne

× Pinder, Corinne

en Pinder, Corinne

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Toda, Takashi

× Toda, Takashi

en Toda, Takashi

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アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
権利情報 © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
主題
主題Scheme Other
主題 fission yeast
主題
主題Scheme Other
主題 microtubule polymerase
主題
主題Scheme Other
主題 XMAP215/TOG
主題
主題Scheme Other
主題 mitotic spindle
主題
主題Scheme Other
主題 spindle pole body
主題
主題Scheme Other
主題 kinetochore
内容記述
内容記述 Proper bipolar spindle assembly underlies accurate chromosome segregation. A cohort of microtubule-associated proteins orchestrates spindle microtubule formation in a spatiotemporally coordinated manner. Among them, the conserved XMAP215/TOG family of microtubule polymerase plays a central role in spindle assembly. In fission yeast, two XMAP215/TOGmembers, Alp14 and Dis1, share essential roles in cell viability; however how these two proteins functionally collaborate remains undetermined. Here we show the functional interplay and specification of Alp14 and Dis1. Creation of new mutant alleles of alp14, which display temperature sensitivity in the absence of Dis1, enabled us to conduct detailed analyses of a double mutant. We have found that simultaneous inactivation of Alp14 and Dis1 results in early mitotic arrest with very short, fragile spindles. Intriguingly, these cells often undergo spindle collapse, leading to a lethal “cut" phenotype. By implementing an artificial targeting system, we have shown that Alp14 and Dis1 are not functionally exchangeable and as such are not merely redundant paralogues. Interestingly, while Alp14 promotes microtubule nucleation, Dis1 does not. Our results uncover that the intrinsic specification, not the spatial regulation, between Alp14 and Dis1 underlies the collaborative actions of these two XMAP215/TOG members in mitotic progression, spindle integrity and genome stability.
言語 en
内容記述
内容記述タイプ Other
内容記述 This work was supported by the Japan Society for the Promotion of Science (JSPS) (KAKENHI Scientific Research (A) 16H02503 and the Program for Advancing Strategic International Networks to Accelerate the Circulation of Talented Researchers (S2902) to T.T. and Scientific Research (C) 19K05813 to M.Y.).
出版者
出版者 MDPI
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ DOI
関連識別子 10.3390/ijms20205108
関連情報
識別子タイプ DOI
関連識別子 https://doi.org/10.3390/ijms20205108
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1661-6596
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1422-0067
開始ページ
開始ページ 5108
書誌情報 International Journal of Molecular Sciences
International Journal of Molecular Sciences

巻 20, 号 20, p. 5108, 発行日 2019-10-15
旧ID 48774
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