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RSC Chromatin-Remodeling Complex Is Important for Mitochondrial Function in Saccharomyces cerevisiae

https://hiroshima.repo.nii.ac.jp/records/2007958
https://hiroshima.repo.nii.ac.jp/records/2007958
f54df217-dc40-4912-a604-ca8f73d7fb76
名前 / ファイル ライセンス アクション
PLoSONE_10_e0130397.pdf PLoSONE_10_e0130397.pdf (1.1 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 RSC Chromatin-Remodeling Complex Is Important for Mitochondrial Function in Saccharomyces cerevisiae
言語 en
作成者 Imamura, Yuko

× Imamura, Yuko

en Imamura, Yuko

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Yu, Feifei

× Yu, Feifei

en Yu, Feifei

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Nakamura, Misaki

× Nakamura, Misaki

en Nakamura, Misaki

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Chihara, Yuhki

× Chihara, Yuhki

en Chihara, Yuhki

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Okane, Kyo

× Okane, Kyo

en Okane, Kyo

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Sato, Masahiro

× Sato, Masahiro

en Sato, Masahiro

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Kanai, Muneyoshi

× Kanai, Muneyoshi

en Kanai, Muneyoshi

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Hamada, Ryoko

× Hamada, Ryoko

en Hamada, Ryoko

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Ueno, Masaru

× Ueno, Masaru

en Ueno, Masaru

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Yukawa, Masashi

× Yukawa, Masashi

en Yukawa, Masashi

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Tsuchiya, Eiko

× Tsuchiya, Eiko

en Tsuchiya, Eiko

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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 © 2015 Imamura et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
内容記述
内容記述 RSC (Remodel the Structure of Chromatin) is an ATP-dependent chromatin remodeling complex essential for the growth of Saccharomyces cerevisiae. RSC exists as two distinct isoforms that share core subunits including the ATPase subunit Nps1/Sth1 but contain either Rsc1or Rsc2. Using the synthetic genetic array (SGA) of the non-essential null mutation method, we screened for mutations exhibiting synthetic growth defects in combination with the temperature-sensitive mutant, nps1-105, and found connections between mitochondrial function and RSC. rsc mutants, including rsc1Δ, rsc2Δ, and nps1-13, another temperature-sensitive nps1 mutant, exhibited defective respiratory growth; in addition, rsc2Δ and nps1-13 contained aggregated mitochondria. The rsc2Δ phenotypes were relieved by RSC1 overexpression, indicating that the isoforms play a redundant role in respiratory growth. Genome-wide expression analysis in nps1-13 under respiratory conditions suggested that RSC regulates the transcription of some target genes of the HAP complex, a transcriptional activator of respiratory gene expression. Nps1 physically interacted with Hap4, the transcriptional activator moiety of the HAP complex, and overexpression of HAP4 alleviated respiratory defects in nps1-13, suggesting that RSC plays pivotal roles in mitochondrial gene expression and shares a set of target genes with the HAP complex.
言語 en
内容記述
内容記述タイプ Other
内容記述 This study was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan to ET (22580086), and MY (19780076); URL: http://www.jsps.go.jp/j-grantsinaid/index.html.
出版者
出版者 Public Library of Science
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 10.1371/journal.pone.0130397
関連情報
識別子タイプ DOI
関連識別子 https://doi.org/10.1371/journal.pone.0130397
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 1932-6203
開始ページ
開始ページ e0130397
書誌情報 PLoS ONE
PLoS ONE

巻 10, 号 6, p. e0130397, 発行日 2015-06-18
旧ID 48776
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