Emerging role of the MORF/MRG gene family in various biological processes, including aging

被引:31
作者
Chen, Meizhen [1 ]
Tominaga, Kaoru [1 ]
Pereira-Smith, Olivia M. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular & Struct Biol, Sam & Ann Barshop Inst Longev & Aging Studies, San Antonio, TX 78245 USA
来源
AGING, CANCER, AND AGE-RELATED DISEASES: COMMON MECHANISM? | 2010年 / 1197卷
关键词
cellular senescence; Mrg (Morf-related genes); MRG15 (Morf-related gene on chromosome 15); chromatin remodeling; neural stem and progenitor cells; DNA damage; aging; HISTONE ACETYLTRANSFERASE COMPLEX; NUCLEAR RECEPTOR TLX; DIPLOID CELL STRAINS; AGE-RELATED DECLINE; NEURAL STEM-CELLS; B-MYB PROMOTER; DENTATE GYRUS; VALPROIC ACID; CHROMO-DOMAIN; TRANSCRIPTIONAL REPRESSION;
D O I
10.1111/j.1749-6632.2010.05197.x
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Cellular senescence is the dominant phenotype over immortality. In our studies to identify senescence-related genes, we cloned Morf4, which induced senescence in a subset of tumor cells. Morf4 is a member of a family of seven genes, and Morf-related genes (Mrg) on chromosomes 15 (Mrg15) and X (MrgX) are also expressed. In contrast to MORF4, MRG15 and MRGX are positive regulators of cell division. All three proteins interact with histone deacetylases and acetyltransferases, suggesting that they function in regulation of chromatin dynamics. Mrg15 knockout mice are embryonic lethal, and mouse embryonic fibroblasts derived from Mrg15 null embryos proliferate poorly, enter senescence rapidly, and have impaired DNA repair compared to the wild type. Mrg15 null embryonic neural stem and progenitor cells also have a decreased capacity for proliferation and differentiation. Further studies are needed to determine the function of this gene family in various biological processes, including neural stem and progenitor cell aging.
引用
收藏
页码:134 / 141
页数:8
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