共 95 条
H2A.Z functions to regulate progression through the cell cycle
被引:74
作者:

Dhillon, N
论文数: 0 引用数: 0
h-index: 0
机构: NICHD, NIH, Unit Chromat & Transcript, Bethesda, MD 20892 USA

Oki, M
论文数: 0 引用数: 0
h-index: 0
机构: NICHD, NIH, Unit Chromat & Transcript, Bethesda, MD 20892 USA

Szyjka, SJ
论文数: 0 引用数: 0
h-index: 0
机构: NICHD, NIH, Unit Chromat & Transcript, Bethesda, MD 20892 USA

Aparicio, OM
论文数: 0 引用数: 0
h-index: 0
机构: NICHD, NIH, Unit Chromat & Transcript, Bethesda, MD 20892 USA

Kamakaka, RT
论文数: 0 引用数: 0
h-index: 0
机构: NICHD, NIH, Unit Chromat & Transcript, Bethesda, MD 20892 USA
机构:
[1] NICHD, NIH, Unit Chromat & Transcript, Bethesda, MD 20892 USA
[2] Univ So Calif, Mol & Computat Biol Program, Los Angeles, CA 90089 USA
关键词:
D O I:
10.1128/MCB.26.2.489-501.2006
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:
Histone H2A variants are highly conserved proteins found ubiquitously in nature and thought to perform specialized functions in the cell. Studies in yeast on the histone H2A variant H2A.Z have shown a role for this protein in transcription as well as chromosome segregation. Our studies have focused on understanding the role of H2A.Z during cell cycle progression. We found that htz1 Delta cells were delayed in DNA replication and progression through the cell cycle. Furthermore, cells lacking H2A.Z required the S-phase checkpoint pathway for survival. We also found that H2A.Z localized to the promoters of cyclin genes, and cells lacking H2A.Z were delayed in the induction of these cyclin genes. Several different models are proposed to explain these observations.
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页码:489 / 501
页数:13
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