期刊
NUCLEIC ACIDS RESEARCH
卷 44, 期 9, 页码 4211-4221出版社
OXFORD UNIV PRESS
DOI: 10.1093/nar/gkw110
关键词
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资金
- Ministry of Education
- Culture, Sports, Science and Technology (MEXT), Japan [23114002]
- Grants-in-Aid for Scientific Research [15K18581] Funding Source: KAKEN
Genome instability triggers cellular senescence and is a common cause of cancer. The ribosomal RNA genes (rDNA), due to their repetitive structure, form a fragile site with frequent rearrangements. To identify eukaryotic factors that connect reduced genome stability to senescence we screened 4,876 strains of a Saccharomyces cerevisiae deletion library for aberrant rDNA and found 708 genes that contribute to its upkeep. 28 mutants caused abnormalities in non-rDNA chromosomes and among them 12 mutants have abnormalities both in rDNA and in non-rDNA chromosomes. Many mutated genes have not previously been implicated with genome maintenance nor their homologues with tumorigenesis in mammals. The link between rDNA state and senescence was broken after deletion of factors related with DNA polymerase epsilon. These mutations also suppressed the short lifespan phenotype of a sir2 mutant, suggesting a model in which molecular events at the heart of the replication fork induce abnormal rDNA recombination and are responsible for the emergence of an aging signal.
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