期刊
GENES TO CELLS
卷 16, 期 4, 页码 467-477出版社
WILEY
DOI: 10.1111/j.1365-2443.2011.01493.x
关键词
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资金
- Ministry of Education, Culture, Sports, Science and Technology
- Japanese Government
- Grants-in-Aid for Scientific Research [22249005] Funding Source: KAKEN
The acetylation of histone H3 on lysine 56 (H3-K56) occurs during S phase and contributes to the processes of DNA damage repair and histone gene transcription. Hst3 and Hst4 have been implicated in the removal of histone H3-K56 acetylation in Saccharomyces cerevisiae. Here, we show that Hst3 and Hst4 regulate the replicative lifespan of S. cerevisiae mother cells. An hst3 Delta hst4 Delta double-mutant strain, in which acetylation of histone H3-K56 persists throughout the genome during the cell cycle, exhibits genomic instability, which is manifested by a loss of heterozygosity with cell aging. Furthermore, we show that in the absence of other proteins Hst3 and Hst4 can deacetylate nucleosomal histone H3-K56 in a nicotinamide adenine dinucleotide(NAD)+-dependent manner. Our results suggest that Hst3 and Hst4 regulate replicative lifespan through their ability to deacetylate histone H3-K56 to minimize genomic instability.
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