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Anatomy of mouse recombination hot spots

Genome-wide analyses have suggested thousands of meiotic recombination hot spots across mammalian genomes. However, very few hot spots have been directly analyzed at a sub-kb scale for crossover (CO) activity. Using recombinant inbred strains as a CO library, here we report the identification and de...

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Detalles Bibliográficos
Autores principales: Wu, Zhen K., Getun, Irina V., Bois, Philippe R. J.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853141/
https://www.ncbi.nlm.nih.gov/pubmed/20081202
http://dx.doi.org/10.1093/nar/gkp1251
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author Wu, Zhen K.
Getun, Irina V.
Bois, Philippe R. J.
author_facet Wu, Zhen K.
Getun, Irina V.
Bois, Philippe R. J.
author_sort Wu, Zhen K.
collection PubMed
description Genome-wide analyses have suggested thousands of meiotic recombination hot spots across mammalian genomes. However, very few hot spots have been directly analyzed at a sub-kb scale for crossover (CO) activity. Using recombinant inbred strains as a CO library, here we report the identification and detailed characterization of seven new meiotic hot spots on mouse chromosome 19, more than doubling the number of currently available mouse hot spots. Although a shared feature is the narrow 1.5–2.5-kb width of these recombinogenic sites, these analyses revealed that hot spots have diverse sequence attributes and distinct symmetric and asymmetric CO profiles. Interestingly, CO molecules with discontinuous conversion tracts are commonly observed, contrasting with those found in human. Furthermore, unlike human hot spots, those present in the mouse do not necessarily have a quasi-normal CO distribution but harbor CO repulsion zones within recombinogenic cores. We propose a model where local chromatin landscape directs these repulsion zones.
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spelling pubmed-28531412010-04-12 Anatomy of mouse recombination hot spots Wu, Zhen K. Getun, Irina V. Bois, Philippe R. J. Nucleic Acids Res Genomics Genome-wide analyses have suggested thousands of meiotic recombination hot spots across mammalian genomes. However, very few hot spots have been directly analyzed at a sub-kb scale for crossover (CO) activity. Using recombinant inbred strains as a CO library, here we report the identification and detailed characterization of seven new meiotic hot spots on mouse chromosome 19, more than doubling the number of currently available mouse hot spots. Although a shared feature is the narrow 1.5–2.5-kb width of these recombinogenic sites, these analyses revealed that hot spots have diverse sequence attributes and distinct symmetric and asymmetric CO profiles. Interestingly, CO molecules with discontinuous conversion tracts are commonly observed, contrasting with those found in human. Furthermore, unlike human hot spots, those present in the mouse do not necessarily have a quasi-normal CO distribution but harbor CO repulsion zones within recombinogenic cores. We propose a model where local chromatin landscape directs these repulsion zones. Oxford University Press 2010-04 2010-01-15 /pmc/articles/PMC2853141/ /pubmed/20081202 http://dx.doi.org/10.1093/nar/gkp1251 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Wu, Zhen K.
Getun, Irina V.
Bois, Philippe R. J.
Anatomy of mouse recombination hot spots
title Anatomy of mouse recombination hot spots
title_full Anatomy of mouse recombination hot spots
title_fullStr Anatomy of mouse recombination hot spots
title_full_unstemmed Anatomy of mouse recombination hot spots
title_short Anatomy of mouse recombination hot spots
title_sort anatomy of mouse recombination hot spots
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2853141/
https://www.ncbi.nlm.nih.gov/pubmed/20081202
http://dx.doi.org/10.1093/nar/gkp1251
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