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Regulation of the DNA damage response on male meiotic sex chromosomes

During meiotic prophase in males, the sex chromosomes partially synapse to form the XY body. This is a unique structure that recruits proteins involved in the DNA damage response, which is believed to be important for silencing of the sex chromosomes. It remains elusive how the DNA damage response i...

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Autores principales: Lu, Lin-Yu, Xiong, Yi, Kuang, Henry, Korakavi, Gautam, Yu, Xiaochun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759350/
https://www.ncbi.nlm.nih.gov/pubmed/23812044
http://dx.doi.org/10.1038/ncomms3105
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author Lu, Lin-Yu
Xiong, Yi
Kuang, Henry
Korakavi, Gautam
Yu, Xiaochun
author_facet Lu, Lin-Yu
Xiong, Yi
Kuang, Henry
Korakavi, Gautam
Yu, Xiaochun
author_sort Lu, Lin-Yu
collection PubMed
description During meiotic prophase in males, the sex chromosomes partially synapse to form the XY body. This is a unique structure that recruits proteins involved in the DNA damage response, which is believed to be important for silencing of the sex chromosomes. It remains elusive how the DNA damage response in the XY body is regulated. H2AX-MDC1-RNF8 signaling, which is well characterized in somatic cells, is dispensable for the recruitment of proteins to the unsynapsed axes in the XY body. However, the DNA damage response that spreads over the sex chromosomes is largely similar to that in somatic cells. Here we show that accumulation of some components of the DNA damage response pathway on the XY body occurs upstream of H2AX-MDC1-RNF8 signalling, and downstream from this cascade of events for others. This analysis shows that there are important differences between the regulation of the DNA damage response at the XY body and at DNA damage sites in somatic cells.
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spelling pubmed-37593502013-12-28 Regulation of the DNA damage response on male meiotic sex chromosomes Lu, Lin-Yu Xiong, Yi Kuang, Henry Korakavi, Gautam Yu, Xiaochun Nat Commun Article During meiotic prophase in males, the sex chromosomes partially synapse to form the XY body. This is a unique structure that recruits proteins involved in the DNA damage response, which is believed to be important for silencing of the sex chromosomes. It remains elusive how the DNA damage response in the XY body is regulated. H2AX-MDC1-RNF8 signaling, which is well characterized in somatic cells, is dispensable for the recruitment of proteins to the unsynapsed axes in the XY body. However, the DNA damage response that spreads over the sex chromosomes is largely similar to that in somatic cells. Here we show that accumulation of some components of the DNA damage response pathway on the XY body occurs upstream of H2AX-MDC1-RNF8 signalling, and downstream from this cascade of events for others. This analysis shows that there are important differences between the regulation of the DNA damage response at the XY body and at DNA damage sites in somatic cells. 2013 /pmc/articles/PMC3759350/ /pubmed/23812044 http://dx.doi.org/10.1038/ncomms3105 Text en Users may view, print, copy, download and 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
Lu, Lin-Yu
Xiong, Yi
Kuang, Henry
Korakavi, Gautam
Yu, Xiaochun
Regulation of the DNA damage response on male meiotic sex chromosomes
title Regulation of the DNA damage response on male meiotic sex chromosomes
title_full Regulation of the DNA damage response on male meiotic sex chromosomes
title_fullStr Regulation of the DNA damage response on male meiotic sex chromosomes
title_full_unstemmed Regulation of the DNA damage response on male meiotic sex chromosomes
title_short Regulation of the DNA damage response on male meiotic sex chromosomes
title_sort regulation of the dna damage response on male meiotic sex chromosomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759350/
https://www.ncbi.nlm.nih.gov/pubmed/23812044
http://dx.doi.org/10.1038/ncomms3105
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