X-Inactivation, Imprinting, and Long Noncoding RNAs in Health and Disease

被引:528
作者
Lee, Jeannie T. [1 ,2 ]
Bartolomei, Marisa S. [3 ]
机构
[1] Massachusetts Gen Hosp, Dept Mol Biol, Howard Hughes Med Inst, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
[3] Univ Penn, Perelman Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
CHROMOSOME INACTIVATION; XIST RNA; FACULTATIVE HETEROCHROMATIN; DOSAGE COMPENSATION; PREIMPLANTATION DEVELOPMENT; SEX-DIFFERENCES; TURNER-SYNDROME; STEM-CELLS; MOUSE; GENE;
D O I
10.1016/j.cell.2013.02.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X chromosome inactivation and genomic imprinting are classic epigenetic processes that cause disease when not appropriately regulated in mammals. Whereas X chromosome inactivation evolved to solve the problem of gene dosage, the purpose of genomic imprinting remains controversial. Nevertheless, the two phenomena are united by allelic control of large gene clusters, such that only one copy of a gene is expressed in every cell. Allelic regulation poses significant challenges because it requires coordinated long-range control in cis and stable propagation over time. Long noncoding RNAs have emerged as a common theme, and their contributions to diseases of imprinting and the X chromosome have become apparent. Here, we review recent advances in basic biology, the connections to disease, and preview potential therapeutic strategies for future development.
引用
收藏
页码:1308 / 1323
页数:16
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