摘要
The CISD2 gene, which is an evolutionarily conserved novel gene, encodes a transmembrane protein primarily associated with the mitochondrial outer membrane. Significantly, the CISD2 gene is located within the candidate region on chromosome 4q where a genetic component for human longevity has been mapped. Previously, we have shown that Cisd2 deficiency shortens lifespan resulting in premature aging in mice. Additionally, an age-dependent decrease in Cisd2 expression has been detected during normal aging. In this study, we demonstrate that a persistent level of Cisd2 achieved by transgenic expression in mice extends their median and maximum lifespan without any apparent deleterious side effects. Cisd2 also ameliorates age-associated degeneration of the skin, skeletal muscles and neurons. Moreover, Cisd2 protects mitochondria from age-associated damage and functional decline as well as attenuating the age-associated reduction in whole-body energy metabolism. These results suggest that Cisd2 is a fundamentally important regulator of lifespan and provide an experimental basis for exploring the candidacy of CISD2 in human longevity.
原文 | 英語 |
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文章編號 | dds210 |
頁(從 - 到) | 3956-3968 |
頁數 | 13 |
期刊 | Human Molecular Genetics |
卷 | 21 |
發行號 | 18 |
DOIs | |
出版狀態 | 已發佈 - 9月 2012 |
對外發佈 | 是 |
ASJC Scopus subject areas
- 遺傳學
- 遺傳學(臨床)
- 分子生物學