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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 2.査読済論文(薬)

Binding of 14-3-3β but not 14-3-3σ controls the cytoplasmic localization of CDC25B: Binding site preferences of 14-3-3 subtypes and the subcellular localization of CDC25B

http://hdl.handle.net/2297/29263
http://hdl.handle.net/2297/29263
ec8a4478-fdf7-43c4-8e15-71038980b921
名前 / ファイル ライセンス アクション
PH-PR-YAMASHITA-K-3011.pdf PH-PR-YAMASHITA-K-3011.pdf (389.8 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-04
タイトル
タイトル Binding of 14-3-3β but not 14-3-3σ controls the cytoplasmic localization of CDC25B: Binding site preferences of 14-3-3 subtypes and the subcellular localization of CDC25B
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
著者 Uchida, Sanae

× Uchida, Sanae

WEKO 27979

Uchida, Sanae

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Kuma, Akiko

× Kuma, Akiko

WEKO 27980

Kuma, Akiko

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Ohtsubo, Motoaki

× Ohtsubo, Motoaki

WEKO 27981

Ohtsubo, Motoaki

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Shimura, Mari

× Shimura, Mari

WEKO 27982

Shimura, Mari

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Hirata, Masato

× Hirata, Masato

WEKO 27983

Hirata, Masato

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Nakagama, Hitoshi

× Nakagama, Hitoshi

WEKO 27984

Nakagama, Hitoshi

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Matsunaga, Tsukasa

× Matsunaga, Tsukasa

WEKO 53
e-Rad 60192340
金沢大学研究者情報 60192340
研究者番号 60192340

Matsunaga, Tsukasa

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Ishizaka, Yukihito

× Ishizaka, Yukihito

WEKO 27985

Ishizaka, Yukihito

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Yamashita, Katsumi

× Yamashita, Katsumi

WEKO 313
金沢大学研究者情報 10191280
研究者番号 10191280

Yamashita, Katsumi

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書誌情報 Journal of Cell Science

巻 117, 号 14, p. 3011-3020, 発行日 2004-06-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-9533
NCID
収録物識別子タイプ NCID
収録物識別子 AA00694823
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1242/jcs.01086
出版者
出版者 Company of Biologists
抄録
内容記述タイプ Abstract
内容記述 The dual specificity phosphatase CDC25B positively controls the G2-M transition by activating CDK1/cyclin B. The binding of 14-3-3 to CDC25B has been shown to regulate the subcellular redistribution of CDC25B from the nucleus to the cytoplasm and may be correlated with the G2 checkpoint. We used a FLAG-tagged version of CDC25B to study the differences among the binding sites for the 14-3-3 subtypes, 14-3-3β, 14-3-3ε and 14-3-3σ, and the relationship between subtype binding and the subcellular localization of CDC25B. All three subtypes were found to bind to CDC25B. Site-directed mutagenesis studies revealed that 14-3-3β bound exclusively near serine-309 of CDC25B1, which is within a potential consensus motif for 14-3-3 binding. By contrast, 14-3-3σ bound preferentially to a site around serine-216, and the presence of serine-137 and -309 enhanced the binding. In addition to these binding-site differences, we found that the binding of 14-3-3β drove CDC25B to the cytoplasm and that mutation of serine-309 to alanine completely abolished the cytoplasmic localization of CDC25B. However, co-expression of 14-3-3σ and CDC25B did not affect the subeellular localization of CDC25B. Furthermore, serine-309 of CDC25B was sufficient to produce its cytoplasmic distribution with co-expression of 14-3-3β, even when other putative 14-3-3 binding sites were mutated. 14-3-3ε resembled 14-3-3β with regard to its binding to CDC25B and the control of CDC25B subcellujar localization. The results of the present study indicite that two 14-3-3 subtypes can control the subcellular localization of CDC25B by binding to a specific site and that 14-3-3σ has effects on CDC25B other than the control of its subcellular localization.
権利
権利情報 © The Company of Biologists Limited 2004
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連URI
識別子タイプ URI
関連識別子 http://jcs.biologists.org/content/117/14/3011
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