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A direct characterization of human mutation based on microsatellites
Mutations are the raw material of evolution, but have been difficult to study directly. We report the largest study of new mutations to date: 2,058 germline changes discovered by analyzing 85,289 Icelanders at 2,477 microsatellites. The paternal-to-maternal mutation rate ratio is 3.3, and the rate i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459271/ https://www.ncbi.nlm.nih.gov/pubmed/22922873 http://dx.doi.org/10.1038/ng.2398 |
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author | Sun, James X. Helgason, Agnar Masson, Gisli Ebenesersdóttir, Sigríđur Sunna Li, Heng Mallick, Swapan Gnerre, Sante Patterson, Nick Kong, Augustine Reich, David Stefansson, Kari |
author_facet | Sun, James X. Helgason, Agnar Masson, Gisli Ebenesersdóttir, Sigríđur Sunna Li, Heng Mallick, Swapan Gnerre, Sante Patterson, Nick Kong, Augustine Reich, David Stefansson, Kari |
author_sort | Sun, James X. |
collection | PubMed |
description | Mutations are the raw material of evolution, but have been difficult to study directly. We report the largest study of new mutations to date: 2,058 germline changes discovered by analyzing 85,289 Icelanders at 2,477 microsatellites. The paternal-to-maternal mutation rate ratio is 3.3, and the rate in fathers doubles from age 20 to 58 whereas there is no association with age in mothers. Longer microsatellite alleles are more mutagenic and tend to decrease in length, whereas the opposite is seen for shorter alleles. We use these empirical observations to build a model that we apply to individuals for whom we have both genome sequence and microsatellite data, allowing us to estimate key parameters of evolution without calibration to the fossil record. We infer that the sequence mutation rate is 1.4–2.3×10(−8) per base pair per generation (90% credible interval), and that human-chimpanzee speciation occurred 3.7–6.6 million years ago. |
format | Online Article Text |
id | pubmed-3459271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-34592712013-04-01 A direct characterization of human mutation based on microsatellites Sun, James X. Helgason, Agnar Masson, Gisli Ebenesersdóttir, Sigríđur Sunna Li, Heng Mallick, Swapan Gnerre, Sante Patterson, Nick Kong, Augustine Reich, David Stefansson, Kari Nat Genet Article Mutations are the raw material of evolution, but have been difficult to study directly. We report the largest study of new mutations to date: 2,058 germline changes discovered by analyzing 85,289 Icelanders at 2,477 microsatellites. The paternal-to-maternal mutation rate ratio is 3.3, and the rate in fathers doubles from age 20 to 58 whereas there is no association with age in mothers. Longer microsatellite alleles are more mutagenic and tend to decrease in length, whereas the opposite is seen for shorter alleles. We use these empirical observations to build a model that we apply to individuals for whom we have both genome sequence and microsatellite data, allowing us to estimate key parameters of evolution without calibration to the fossil record. We infer that the sequence mutation rate is 1.4–2.3×10(−8) per base pair per generation (90% credible interval), and that human-chimpanzee speciation occurred 3.7–6.6 million years ago. 2012-08-23 2012-10 /pmc/articles/PMC3459271/ /pubmed/22922873 http://dx.doi.org/10.1038/ng.2398 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 Sun, James X. Helgason, Agnar Masson, Gisli Ebenesersdóttir, Sigríđur Sunna Li, Heng Mallick, Swapan Gnerre, Sante Patterson, Nick Kong, Augustine Reich, David Stefansson, Kari A direct characterization of human mutation based on microsatellites |
title | A direct characterization of human mutation based on microsatellites |
title_full | A direct characterization of human mutation based on microsatellites |
title_fullStr | A direct characterization of human mutation based on microsatellites |
title_full_unstemmed | A direct characterization of human mutation based on microsatellites |
title_short | A direct characterization of human mutation based on microsatellites |
title_sort | direct characterization of human mutation based on microsatellites |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3459271/ https://www.ncbi.nlm.nih.gov/pubmed/22922873 http://dx.doi.org/10.1038/ng.2398 |
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