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

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 fl...

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Autores principales: Brown, Emily J., Nguyen, Alison H., Bachtrog, Doris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274899/
https://www.ncbi.nlm.nih.gov/pubmed/32313175
http://dx.doi.org/10.1038/s41559-020-1179-5
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author Brown, Emily J.
Nguyen, Alison H.
Bachtrog, Doris
author_facet Brown, Emily J.
Nguyen, Alison H.
Bachtrog, Doris
author_sort Brown, Emily J.
collection PubMed
description 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 shorter average life spans 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 aging. This is associated with a loss of heterochromatin at repetitive elements during aging 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; 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 aging in flies.
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spelling pubmed-72748992020-10-20 The Y chromosome may contribute to sex-specific aging in Drosophila Brown, Emily J. Nguyen, Alison H. Bachtrog, Doris Nat Ecol Evol Article 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 shorter average life spans 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 aging. This is associated with a loss of heterochromatin at repetitive elements during aging 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; 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 aging in flies. 2020-04-20 2020-06 /pmc/articles/PMC7274899/ /pubmed/32313175 http://dx.doi.org/10.1038/s41559-020-1179-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Brown, Emily J.
Nguyen, Alison H.
Bachtrog, Doris
The Y chromosome may contribute to sex-specific aging in Drosophila
title The Y chromosome may contribute to sex-specific aging in Drosophila
title_full The Y chromosome may contribute to sex-specific aging in Drosophila
title_fullStr The Y chromosome may contribute to sex-specific aging in Drosophila
title_full_unstemmed The Y chromosome may contribute to sex-specific aging in Drosophila
title_short The Y chromosome may contribute to sex-specific aging in Drosophila
title_sort y chromosome may contribute to sex-specific aging in drosophila
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7274899/
https://www.ncbi.nlm.nih.gov/pubmed/32313175
http://dx.doi.org/10.1038/s41559-020-1179-5
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