Sharma Ramesh, Nakamura Akihiro, Takahashi Ryoya, Nakamoto Hideko, Goto Sataro
Department of Biochemistry, Faculty of Pharmaceutical Sciences, Toho University, Miyama 2-2-1, Funabashi, Chiba 274-8510, Japan.
Free Radic Biol Med. 2006 Apr 1;40(7):1179-84. doi: 10.1016/j.freeradbiomed.2005.11.013. Epub 2005 Dec 1.
We studied carbonylation, a form of oxidative modification of proteins, of histones in rat livers. Histones H1, H2B/H2A, and H3 were significantly carbonylated but the modification was almost undetectable in H4. Contrary to the generally accepted view of increased protein carbonylation with age, the modification of histones was significantly lower in old (30-month-old) than in young (5-month-old) animals. Dietary restriction of older animals for 2 months resulted in increase in carbonylation comparable to that at the young level. These findings may have physiological implications in chromatin structure/function in aging and beneficial effects of DR by influencing transcription, replication, and/or repair activities.
我们研究了大鼠肝脏中组蛋白的羰基化作用,这是蛋白质氧化修饰的一种形式。组蛋白H1、H2B/H2A和H3发生了显著的羰基化,但在H4中几乎检测不到这种修饰。与普遍认为的蛋白质羰基化随年龄增长而增加的观点相反,老年(30月龄)动物组蛋白的修饰显著低于幼年(5月龄)动物。对老年动物进行2个月的饮食限制导致羰基化增加,与幼年水平相当。这些发现可能对衰老过程中染色质结构/功能具有生理意义,并通过影响转录、复制和/或修复活动对饮食限制的有益作用产生影响。