Characterization of the gene encoding mouse retinoblastoma binding protein-7, a component of chromatin-remodeling complexes

被引:17
|
作者
Yang, J [1 ]
Kiefer, SM [1 ]
Rauchman, M [1 ]
机构
[1] Washington Univ, Sch Med, Div Renal, St Louis, MO 63110 USA
关键词
retinoblastoma binding protein 7 (RBBP7); retinoblastoma-associated protein 46 (RBAP46); CAF1; LIN-53; RBA-1; histone deacetylase (HDAC); transcriptional repression; chromatin remodeling; SIN3A; NURD; X-linked mental retardation (XLMR);
D O I
10.1006/geno.2002.6844
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RBBP7 is a highly conserved WD-repeat protein that interacts with histone deacetylases and is a component of several co-repressor complexes. The mouse gene Rbbp7 spans similar to20 kb, consists of at least 12 exons, and contains a C/T polymorphism in the 3' splice acceptor region of intron 3. We found that Rbbp7 contains a TATA-less promoter with multiple transcription initiation sites. In transient transfection assays, we identified potential positive regulatory elements upstream of the proximal promoter at -668 to -1710. RBBP7 protein is detectable from at least day 9.5 of embryogenesis and is strongly expressed in the developing kidney and brain. Consistent with its association with co-repressor complexes, we demonstrate that RBBP7 represses the c-FOS transactivation domain in response to mitogen stimulation. We have also excluded human RBBP7 as a candidate gene in six patients that exhibit X-linked mental retardation, a heterogeneous developmental disorder that has been linked in some cases to mutations in genes involved in chromatin remodeling.
引用
收藏
页码:407 / 415
页数:9
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