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Sfh1p, a Component of a Novel Chromatin-Remodeling Complex, Is Required for Cell Cycle Progression
Author(s) -
Yixue Cao,
Bradley R. Cairns,
Roger D. Kornberg,
Brehon C. Laurent
Publication year - 1997
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.17.6.3323
Subject(s) - biology , chromatin structure remodeling (rsc) complex , chromatin , chromatin remodeling , nucleosome , microbiology and biotechnology , saccharomyces cerevisiae , cell cycle , genetics , swi/snf , cell division , dna , cell , yeast
Several eukaryotic multiprotein complexes, including the Saccharomyces cerevisiae Snf/Swi complex, remodel chromatin for transcription. In contrast to the Snf/Swi proteins, Sfh1p, a new Snf5p paralog, is essential for viability. The evolutionarily conserved domain of Sfh1p is sufficient for normal function, and Sfh1p interacts functionally and physically with an essential Snf2p paralog in a novel nucleosome-restructuring complex called RSC (for remodels the structure of chromatin). A temperature-sensitive sfh1 allele arrests cells in the G2/M phase of the cell cycle, and the Sfh1 protein is specifically phosphorylated in the G1 phase. Together, these results demonstrate a link between chromatin remodeling and progression through the cell division cycle, providing genetic clues to possible targets for RSC function.

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