eXIST with matrix-associated proteins

被引:14
|
作者
Nakagawa, Shinichi [1 ,2 ]
Prasanth, Kannanganattu V. [3 ]
机构
[1] RIKEN, Adv Res Inst, RNA Biol Lab, Wako, Saitama 3510198, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Univ Illinois, Chem & Life Sci Lab, Dept Cell & Dev Biol, Urbana, IL 61801 USA
关键词
X-CHROMOSOME INACTIVATION; ATTACHMENT REGION DNA; LONG NONCODING RNAS; XIST RNA; NUCLEAR-MATRIX; BINDING-PROTEIN; GENE-EXPRESSION; IN-VIVO; SAF-A; HNRNP U;
D O I
10.1016/j.tcb.2011.02.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
X-chromosome inactivation has long served as an experimental model system for understanding the epigenetic regulation of gene expression. Central to this phenomenon is the long, non-coding RNA Xist that is specifically expressed from the inactive X chromosome and spreads along the entire length of the chromosome in cis. Recently, two of the proteins originally identified as components of the nuclear scaffold/matrix (S/MAR-associated proteins) have been shown to control the principal features of X-chromosome inactivation; specifically, context-dependent competency and the chromosome-wide association of Xist RNA. These findings implicate the involvement of nuclear S/MAR-associated proteins in the organization of epigenetic machinery. Here, we describe a model for the functional role of S/MAR-associated proteins in the regulation of key epigenetic processes.
引用
收藏
页码:321 / 327
页数:7
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