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After chromatin is SWItched-on can it be RUSHed?
被引:10
作者:
Devine, JH
[1
]
Hewetson, A
[1
]
Lee, VH
[1
]
Chilton, BS
[1
]
机构:
[1] Texas Tech Univ, Hlth Sci Ctr, Lubbock, TX 79430 USA
关键词:
SWI SNF;
chromatin remodeling;
prolactin;
progesterone;
uteroglobin gene transcription;
RUSH proteins;
RING-finger motif;
alternative splicing;
D O I:
10.1016/S0303-7207(99)00013-1
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Repressive chromatin must be remodeled to allow for transcriptional activation of genes in eukaryotic cells. Factors that alter chromatin structure to permit access of transcriptional activators, RNA polymerase II and the polymerase-associated general transcription factors to nucleosomal promoter sequences are as highly conserved as the basic mechanism of transcription. One group of promoter restructuring factors that perturbs chromatin in an ATP-dependent manner includes NURF, CHRAC, ACF, the SWI/SNF complex, and SWI/SNF-related proteins. Each member of this group contains a subunit homologous to the DNA-dependent ATPase; however, their individual mechanisms of action are unique. The small amount of SWI/SNF complex (100-200 copies/cell), its affiliation with a select number of inducible genes, and its interaction with the glucocorticoid and estrogen receptors, suggests the SWI/SNF complex might be preferentially targeted to active promoters. The SWI/SNF-related family of RUSH proteins which includes RUSH-1 alpha and beta, hHLTF, HIP116, Zbu1, P113, and the transcription factor RUSH-la isolog has been implicated as a highly conserved DNA binding site-specific ATPase. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
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页码:49 / 56
页数:8
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