A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis
Male spermatogenesis is an essential and complex process necessary to gain totipotency and allow a whole new organism to develop upon fertilization. While single-gene based studies have provided insights into the mechanisms underlying spermatogenesis, detailed global profiling of all the key meiotic...
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pubmed-39662192014-03-26 A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis Fallahi, Mohammad Getun, Irina V. Wu, Zhen K. Bois, Philippe R.J. Article Male spermatogenesis is an essential and complex process necessary to gain totipotency and allow a whole new organism to develop upon fertilization. While single-gene based studies have provided insights into the mechanisms underlying spermatogenesis, detailed global profiling of all the key meiotic stages is required to fully define these processes. Here, by isolating highly enriched mouse meiotic cell populations, we have generated a comprehensive gene expression atlas of mammalian meiosis. Our data define unique signatures for the specific stages of meiosis, including global chromosome X inactivation and reactivation. The data also reveal profound switches in global gene expression at the initiation of pachynema that are reminiscent of the commitment to meiosis observed in budding yeast. Overall, this meiotic atlas provides an exhaustive blueprint and resource for mammalian gametogenesis and meiosis. MDPI 2010-12-13 /pmc/articles/PMC3966219/ /pubmed/24710097 http://dx.doi.org/10.3390/genes1030469 Text en © 2010 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Fallahi, Mohammad Getun, Irina V. Wu, Zhen K. Bois, Philippe R.J. |
spellingShingle |
Fallahi, Mohammad Getun, Irina V. Wu, Zhen K. Bois, Philippe R.J. A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis |
author_facet |
Fallahi, Mohammad Getun, Irina V. Wu, Zhen K. Bois, Philippe R.J. |
author_sort |
Fallahi, Mohammad |
title |
A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis |
title_short |
A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis |
title_full |
A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis |
title_fullStr |
A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis |
title_full_unstemmed |
A Global Expression Switch Marks Pachytene Initiation during Mouse Male Meiosis |
title_sort |
global expression switch marks pachytene initiation during mouse male meiosis |
description |
Male spermatogenesis is an essential and complex process necessary to gain totipotency and allow a whole new organism to develop upon fertilization. While single-gene based studies have provided insights into the mechanisms underlying spermatogenesis, detailed global profiling of all the key meiotic stages is required to fully define these processes. Here, by isolating highly enriched mouse meiotic cell populations, we have generated a comprehensive gene expression atlas of mammalian meiosis. Our data define unique signatures for the specific stages of meiosis, including global chromosome X inactivation and reactivation. The data also reveal profound switches in global gene expression at the initiation of pachynema that are reminiscent of the commitment to meiosis observed in budding yeast. Overall, this meiotic atlas provides an exhaustive blueprint and resource for mammalian gametogenesis and meiosis. |
publisher |
MDPI |
publishDate |
2010 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966219/ |
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1612071366247317504 |