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Regulation of human flap endonuclease-1 activity by acetylation through the transcriptional coactivator p300
被引:140
作者:

Hasan, S
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Stucki, M
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Hassa, PO
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Imhof, R
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Gehrig, P
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Hunziker, P
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Hübscher, U
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland

Hottiger, MO
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机构: Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland
机构:
[1] Univ Zurich, Inst Vet Biochem, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland
关键词:
D O I:
10.1016/S1097-2765(01)00272-6
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
We describe a role for the transcriptional coactivator p300 in DNA metabolism, p300 formed a complex with flap endonuclease-1 (Fen1) and acetylated Fen1 in vitro. Furthermore, Fen1 acetylation was observed in vivo and was enhanced upon UV treatment of human cells. Remarkably, acetylation of the Fen1 C terminus by p300 significantly reduced Fen1's DNA binding and nuclease activity. Proliferating cell nuclear antigen (PCNA) was able to stimulate both acetylated and unacetylated Fen1 activity to the same extent. Our results identify acetylation as a novel regulatory modification of Fen1 and implicate that p300 is not only a component of the chromatin remodeling machinery but might also play a critical role in regulating DNA metabolic events.
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页码:1221 / 1231
页数:11
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