期刊
MOLECULAR CELL
卷 34, 期 5, 页码 620-626出版社
CELL PRESS
DOI: 10.1016/j.molcel.2009.04.014
关键词
-
资金
- Mi-2. B.P.R [F32GM74527, F32GM76936]
- National Research Service Award (NRSA)
- National Institutes of Health (NIH) [GM058272]
The high-mobility group N (HMGN) proteins are abundant nonhistone chromosomal proteins that bind specifically to nucleosomes at two high-affinity sites. Here we report that purified recombinant human HMGN1 (HMG14) and HMGN2 (HMG17) potently repress ATIP-dependent chromatin remodeling by four different molecular motor proteins. In contrast, mutant HMGN proteins with double Ser-to-Glu mutations in their nucleosome-binding domains are unable to inhibit chromatin remodeling. The HMGN-mediated repression of chromatin remodeling is reversible and dynamic. With the ACF chromatin remodeling factor, HMGN2 does not directly inhibit the ATPase activity but rather appears to reduce the affinity of the factor to chromatin. These findings suggest that HMGN proteins serve as a counterbalance to the action of the many ATIP-dependent chromatin remodeling activities in the nucleus.
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