Networking in the nucleus: a spotlight on LEM-domain proteins

被引:137
作者
Barton, Lacy J. [1 ,2 ]
Soshnev, Alexey A. [3 ]
Geyer, Pamela K. [1 ]
机构
[1] Univ Iowa, Coll Med, Dept Biochem, Iowa City, IA 52242 USA
[2] NYU, Langone Med Ctr, Sch Med, Skirball Inst,Dept Cell Biol, New York, NY 10016 USA
[3] Rockefeller Univ, Lab Chromatin Biol & Epigenet, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
SATELLITE CELL-DIFFERENTIATION; DREIFUSS MUSCULAR-DYSTROPHY; DEACETYLASE; 3; HDAC3; MEMBRANE PROTEIN; CAENORHABDITIS-ELEGANS; ENVELOPE PROTEIN; LAMIN-A/C; POLYPEPTIDE (LAP)2-ALPHA; MOLECULAR-BASIS; ESSENTIAL ROLES;
D O I
10.1016/j.ceb.2015.03.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proteins resident in the inner nuclear membrane and underlying nuclear lamina form a network that regulates nuclear functions. This review highlights a prominent family of nuclear lamina proteins that carries the LAP2-emerin-MAN1-domain (LEM-D). LEM-D proteins share an ability to bind lamins and tether repressive chromatin at the nuclear periphery. The importance of this family is underscored by findings that loss of individual LEM-D proteins causes progressive, tissue-restricted diseases, known as laminopathies. Diverse functions of LEM-D proteins are linked to interactions with unique and overlapping partners including signal transduction effectors, transcription factors and architectural proteins. Recent investigations suggest that LEM-D proteins form hubs within the nuclear lamina that integrate external signals important for tissue homeostasis and maintenance of progenitor cell populations.
引用
收藏
页码:1 / 8
页数:8
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