早熟
拉明
生物
早衰
遗传学
LMNA公司
核板
组蛋白
细胞核
细胞生物学
核蛋白
DNA
基因
转录因子
作者
Paola Scaffidi,Tom Misteli
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2006-05-19
卷期号:312 (5776): 1059-1063
被引量:1039
标识
DOI:10.1126/science.1127168
摘要
Mutations in the nuclear structural protein lamin A cause the premature aging syndrome Hutchinson-Gilford progeria (HGPS). Whether lamin A plays any role in normal aging is unknown. We show that the same molecular mechanism responsible for HGPS is active in healthy cells. Cell nuclei from old individuals acquire defects similar to those of HGPS patient cells, including changes in histone modifications and increased DNA damage. Age-related nuclear defects are caused by sporadic use, in healthy individuals, of the same cryptic splice site in lamin A whose constitutive activation causes HGPS. Inhibition of this splice site reverses the nuclear defects associated with aging. These observations implicate lamin A in physiological aging.
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