4.5 Article

The Y chromosome may contribute to sex-specific ageing in Drosophila

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NATURE ECOLOGY & EVOLUTION
卷 4, 期 6, 页码 853-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41559-020-1179-5

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  1. NIH [R01GM076007, GM101255, R01AG057029]

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Heterochromatin suppresses repetitive DNA, and a loss of heterochromatin has been observed in aged cells of several species, including humans and Drosophila. Males often contain substantially more heterochromatic DNA than females, due to the presence of a large, repeat-rich Y chromosome, and male flies generally have a shorter average lifespan than females. Here we show that repetitive DNA becomes de-repressed more rapidly in old male flies relative to females, and repeats on the Y chromosome are disproportionally mis-expressed during ageing. This is associated with a loss of heterochromatin at repetitive elements during ageing in male flies, and a general loss of repressive chromatin in aged males away from pericentromeric regions and the Y. By generating flies with different sex chromosome karyotypes (XXY females and X0 and XYY males), we show that repeat de-repression and average lifespan is correlated with the number of Y chromosomes. This suggests that sex-specific chromatin differences may contribute to sex-specific ageing in flies. Flies with different numbers of Y chromosomes are used to show a potential link between de-repression of repetitive DNA and ageing.

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