Analysis of the cell cycle regulation of chromosome condensation protein complex, condensin.
Project/Area Number |
15370091
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Cell biology
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Research Institution | RIKEN |
Principal Investigator |
KIMURA Keiji RIKEN, Cellular Physiology Laboratory, Staff Scientist, 花岡細胞生理学研究室, 先任研究員 (50332268)
|
Project Period (FY) |
2003 – 2005
|
Project Status |
Completed (Fiscal Year 2005)
|
Budget Amount *help |
¥15,100,000 (Direct Cost: ¥15,100,000)
Fiscal Year 2005: ¥4,400,000 (Direct Cost: ¥4,400,000)
Fiscal Year 2004: ¥4,400,000 (Direct Cost: ¥4,400,000)
Fiscal Year 2003: ¥6,300,000 (Direct Cost: ¥6,300,000)
|
Keywords | condensin / SMC / phosphorylation / chromatin / chromosome condensation / cell cycle / Cdc2 / CK2 / クロマチン構造 / SMCタンパク質 / Cdc2キナーゼ / カゼインキナーゼII / HeLa細胞 / 細胞分裂期 / 染色体分配 |
Research Abstract |
Condensin, a conserved pentameric protein complex composed of SMC heterodimer (SMC2/CAP-E and SMC4/CAP-E) and three other non-SMC subunits (CAP-D2, -G, and -H), plays an essential role in mitotic chromosome condensation in vivo. Condensin induces positive supercoiling into DNA in the presence of topo I using the energy of ATP hydrolysis in vitro. In addition to their mitotic functions, condensins have been implicated in chromatin regulation during interphase, such as DNA repair, damage checkpoint response and transcriptional regulation. We analyzed precisely cell cycle regulation of condensin complex. The protein levels and stabilities of condensin subunits were almost constant throughout the cell cycle. Condensin was phosphorylated by Cdc2 during mitosis, and by CK2 during interphase. In contrast to the stimulatory effect of Cdc2-induced phosphorylation of condensin I on supercoiling, phosphorylation by CK2 reduced the supercoiling activity of condensin I. CK2-mediated phosphorylation of condensin I is spatially and temporally regulated in a manner different to that of Cdc2-mediated phosphorylation : CK2-dependent phosphorylation increases during interphase and decreases on chromosomes during mitosis. These findings are the first to demonstrate a negative regulatory mode for condensin I, a process that may influence chromatin structure during interphase and mitosis. When condensin was added into in vitro transcription system, transcription level was reduced, and the suppression was cancelled by the CK2-mediated phosphorylation. Thus, it is possible chromatin structure was compacted by condensin during interphase, and inhibition of condensin activity by the CK2-mediated phosphorylation leads to relaxation of chromatin structure and transactivation.
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Report
(4 results)
Research Products
(10 results)
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[Journal Article] Direct association with inner centromere prptein (INCENP) activates the novel chromosomal passenger protein, Aurora-C2004
Author(s)
Li, X., Sakashita, G., Matsuzaki, H., Sugimoto, K., Kimura, K., Hanaoka, F., Taninguchi, H., Furukawa, K., Urano, T.
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Journal Title
The journal of biological chemistry 279・45
Pages: 47201-47211
Description
「研究成果報告書概要(和文)」より
Related Report
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[Journal Article] Direct association with inner centromere protein (INCENP) activates the novel chromosomal passenger protein, Aurora-C.2004
Author(s)
Li, X., Sakashita, G., Matsuzaki, H., Sugimoto, K., Kimura, K., Hanaoka, F., Taniguchi, H., Furukawa, K., Urano, T.
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Journal Title
J.Biol.Chem. 279
Pages: 47201-47211
Description
「研究成果報告書概要(欧文)」より
Related Report
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[Journal Article] Direct association with inner centromere prptein(INCENP) activates the novel chromosomal passenger protein, Aurora-C2004
Author(s)
Li, X., Sakashita, G., Matsuzaki, H., Sugimoto, K., Kimura, K., Hanaoka, F., Taniguchi, H., Furukawa, K., Urano, T.
-
Journal Title
J.Biol.Chem. 279・45
Pages: 47201-47211
Related Report
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