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The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle

Inhibitors of microtubule (MT) assembly or dynamics that target α/β-tubulin are widely exploited in cancer therapy and biological research. However, specific inhibitors of the MT nucleator γ-tubulin that would allow testing temporal functions of γ-tubulin during the cell cycle are yet to be identifi...

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Autores principales: Chinen, Takumi, Liu, Peng, Shioda, Shuya, Pagel, Judith, Cerikan, Berati, Lin, Tien-chen, Gruss, Oliver, Hayashi, Yoshiki, Takeno, Haruka, Shima, Tomohiro, Okada, Yasushi, Hayakawa, Ichiro, Hayashi, Yoshio, Kigoshi, Hideo, Usui, Takeo, Schiebel, Elmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640066/
https://www.ncbi.nlm.nih.gov/pubmed/26503935
http://dx.doi.org/10.1038/ncomms9722
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author Chinen, Takumi
Liu, Peng
Shioda, Shuya
Pagel, Judith
Cerikan, Berati
Lin, Tien-chen
Gruss, Oliver
Hayashi, Yoshiki
Takeno, Haruka
Shima, Tomohiro
Okada, Yasushi
Hayakawa, Ichiro
Hayashi, Yoshio
Kigoshi, Hideo
Usui, Takeo
Schiebel, Elmar
author_facet Chinen, Takumi
Liu, Peng
Shioda, Shuya
Pagel, Judith
Cerikan, Berati
Lin, Tien-chen
Gruss, Oliver
Hayashi, Yoshiki
Takeno, Haruka
Shima, Tomohiro
Okada, Yasushi
Hayakawa, Ichiro
Hayashi, Yoshio
Kigoshi, Hideo
Usui, Takeo
Schiebel, Elmar
author_sort Chinen, Takumi
collection PubMed
description Inhibitors of microtubule (MT) assembly or dynamics that target α/β-tubulin are widely exploited in cancer therapy and biological research. However, specific inhibitors of the MT nucleator γ-tubulin that would allow testing temporal functions of γ-tubulin during the cell cycle are yet to be identified. By evolving β-tubulin-binding drugs we now find that the glaziovianin A derivative gatastatin is a γ-tubulin-specific inhibitor. Gatastatin decreased interphase MT dynamics of human cells without affecting MT number. Gatastatin inhibited assembly of the mitotic spindle in prometaphase. Addition of gatastatin to preformed metaphase spindles altered MT dynamics, reduced the number of growing MTs and shortened spindle length. Furthermore, gatastatin prolonged anaphase duration by affecting anaphase spindle structure, indicating the continuous requirement of MT nucleation during mitosis. Thus, gatastatin facilitates the dissection of the role of γ-tubulin during the cell cycle and reveals the sustained role of γ-tubulin.
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spelling pubmed-46400662015-12-08 The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle Chinen, Takumi Liu, Peng Shioda, Shuya Pagel, Judith Cerikan, Berati Lin, Tien-chen Gruss, Oliver Hayashi, Yoshiki Takeno, Haruka Shima, Tomohiro Okada, Yasushi Hayakawa, Ichiro Hayashi, Yoshio Kigoshi, Hideo Usui, Takeo Schiebel, Elmar Nat Commun Article Inhibitors of microtubule (MT) assembly or dynamics that target α/β-tubulin are widely exploited in cancer therapy and biological research. However, specific inhibitors of the MT nucleator γ-tubulin that would allow testing temporal functions of γ-tubulin during the cell cycle are yet to be identified. By evolving β-tubulin-binding drugs we now find that the glaziovianin A derivative gatastatin is a γ-tubulin-specific inhibitor. Gatastatin decreased interphase MT dynamics of human cells without affecting MT number. Gatastatin inhibited assembly of the mitotic spindle in prometaphase. Addition of gatastatin to preformed metaphase spindles altered MT dynamics, reduced the number of growing MTs and shortened spindle length. Furthermore, gatastatin prolonged anaphase duration by affecting anaphase spindle structure, indicating the continuous requirement of MT nucleation during mitosis. Thus, gatastatin facilitates the dissection of the role of γ-tubulin during the cell cycle and reveals the sustained role of γ-tubulin. Nature Pub. Group 2015-10-27 /pmc/articles/PMC4640066/ /pubmed/26503935 http://dx.doi.org/10.1038/ncomms9722 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Chinen, Takumi
Liu, Peng
Shioda, Shuya
Pagel, Judith
Cerikan, Berati
Lin, Tien-chen
Gruss, Oliver
Hayashi, Yoshiki
Takeno, Haruka
Shima, Tomohiro
Okada, Yasushi
Hayakawa, Ichiro
Hayashi, Yoshio
Kigoshi, Hideo
Usui, Takeo
Schiebel, Elmar
The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
title The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
title_full The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
title_fullStr The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
title_full_unstemmed The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
title_short The γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
title_sort γ-tubulin-specific inhibitor gatastatin reveals temporal requirements of microtubule nucleation during the cell cycle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640066/
https://www.ncbi.nlm.nih.gov/pubmed/26503935
http://dx.doi.org/10.1038/ncomms9722
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