The distribution and causes of meiotic recombination in the human genome.

Using the statistical analysis of genetic variation, we have developed a high-resolution genetic map of recombination hotspots and recombination rate variation across the human genome. This map, which has a resolution several orders of magnitude greater than previous studies, identifies over 25,000...

Full description

Bibliographic Details
Main Authors: Myers, S, Spencer, C, Auton, A, Bottolo, L, Freeman, C, Donnelly, P, McVean, G
Format: Journal article
Language:English
Published: 2006
_version_ 1797068182531342336
author Myers, S
Spencer, C
Auton, A
Bottolo, L
Freeman, C
Donnelly, P
McVean, G
author_facet Myers, S
Spencer, C
Auton, A
Bottolo, L
Freeman, C
Donnelly, P
McVean, G
author_sort Myers, S
collection OXFORD
description Using the statistical analysis of genetic variation, we have developed a high-resolution genetic map of recombination hotspots and recombination rate variation across the human genome. This map, which has a resolution several orders of magnitude greater than previous studies, identifies over 25,000 recombination hotspots and gives new insights into the distribution and determination of recombination. Wavelet-based analysis demonstrates scale-specific influences of base composition, coding context and DNA repeats on recombination rates, though, in contrast with other species, no association with DNase I hypersensitivity. We have also identified specific DNA motifs that are strongly associated with recombination hotspots and whose activity is influenced by local context. Comparative analysis of recombination rates in humans and chimpanzees demonstrates very high rates of evolution of the fine-scale structure of the recombination landscape. In the light of these observations, we suggest possible resolutions of the hotspot paradox.
first_indexed 2024-03-06T22:07:01Z
format Journal article
id oxford-uuid:50838c9c-8b56-46f8-bf66-e5f12c543cd3
institution University of Oxford
language English
last_indexed 2024-03-06T22:07:01Z
publishDate 2006
record_format dspace
spelling oxford-uuid:50838c9c-8b56-46f8-bf66-e5f12c543cd32022-03-26T16:13:56ZThe distribution and causes of meiotic recombination in the human genome.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:50838c9c-8b56-46f8-bf66-e5f12c543cd3EnglishSymplectic Elements at Oxford2006Myers, SSpencer, CAuton, ABottolo, LFreeman, CDonnelly, PMcVean, GUsing the statistical analysis of genetic variation, we have developed a high-resolution genetic map of recombination hotspots and recombination rate variation across the human genome. This map, which has a resolution several orders of magnitude greater than previous studies, identifies over 25,000 recombination hotspots and gives new insights into the distribution and determination of recombination. Wavelet-based analysis demonstrates scale-specific influences of base composition, coding context and DNA repeats on recombination rates, though, in contrast with other species, no association with DNase I hypersensitivity. We have also identified specific DNA motifs that are strongly associated with recombination hotspots and whose activity is influenced by local context. Comparative analysis of recombination rates in humans and chimpanzees demonstrates very high rates of evolution of the fine-scale structure of the recombination landscape. In the light of these observations, we suggest possible resolutions of the hotspot paradox.
spellingShingle Myers, S
Spencer, C
Auton, A
Bottolo, L
Freeman, C
Donnelly, P
McVean, G
The distribution and causes of meiotic recombination in the human genome.
title The distribution and causes of meiotic recombination in the human genome.
title_full The distribution and causes of meiotic recombination in the human genome.
title_fullStr The distribution and causes of meiotic recombination in the human genome.
title_full_unstemmed The distribution and causes of meiotic recombination in the human genome.
title_short The distribution and causes of meiotic recombination in the human genome.
title_sort distribution and causes of meiotic recombination in the human genome
work_keys_str_mv AT myerss thedistributionandcausesofmeioticrecombinationinthehumangenome
AT spencerc thedistributionandcausesofmeioticrecombinationinthehumangenome
AT autona thedistributionandcausesofmeioticrecombinationinthehumangenome
AT bottolol thedistributionandcausesofmeioticrecombinationinthehumangenome
AT freemanc thedistributionandcausesofmeioticrecombinationinthehumangenome
AT donnellyp thedistributionandcausesofmeioticrecombinationinthehumangenome
AT mcveang thedistributionandcausesofmeioticrecombinationinthehumangenome
AT myerss distributionandcausesofmeioticrecombinationinthehumangenome
AT spencerc distributionandcausesofmeioticrecombinationinthehumangenome
AT autona distributionandcausesofmeioticrecombinationinthehumangenome
AT bottolol distributionandcausesofmeioticrecombinationinthehumangenome
AT freemanc distributionandcausesofmeioticrecombinationinthehumangenome
AT donnellyp distributionandcausesofmeioticrecombinationinthehumangenome
AT mcveang distributionandcausesofmeioticrecombinationinthehumangenome