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Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice
The germline mutation rate is an important parameter that affects the amount of genetic variation and the rate of evolution. However, neither the rate of germline mutations in laboratory mice nor the biological significance of the mutation rate in mammalian populations is clear. Here we studied geno...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509997/ https://www.ncbi.nlm.nih.gov/pubmed/26129709 http://dx.doi.org/10.1101/gr.186148.114 |
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author | Uchimura, Arikuni Higuchi, Mayumi Minakuchi, Yohei Ohno, Mizuki Toyoda, Atsushi Fujiyama, Asao Miura, Ikuo Wakana, Shigeharu Nishino, Jo Yagi, Takeshi |
author_facet | Uchimura, Arikuni Higuchi, Mayumi Minakuchi, Yohei Ohno, Mizuki Toyoda, Atsushi Fujiyama, Asao Miura, Ikuo Wakana, Shigeharu Nishino, Jo Yagi, Takeshi |
author_sort | Uchimura, Arikuni |
collection | PubMed |
description | The germline mutation rate is an important parameter that affects the amount of genetic variation and the rate of evolution. However, neither the rate of germline mutations in laboratory mice nor the biological significance of the mutation rate in mammalian populations is clear. Here we studied genome-wide mutation rates and the long-term effects of mutation accumulation on phenotype in more than 20 generations of wild-type C57BL/6 mice and mutator mice, which have high DNA replication error rates. We estimated the base-substitution mutation rate to be 5.4 × 10(−9) (95% confidence interval = 4.6 × 10(−9)–6.5 × 10(−9)) per nucleotide per generation in C57BL/6 laboratory mice, about half the rate reported in humans. The mutation rate in mutator mice was 17 times that in wild-type mice. Abnormal phenotypes were 4.1-fold more frequent in the mutator lines than in the wild-type lines. After several generations, the mutator mice reproduced at substantially lower rates than the controls, exhibiting low pregnancy rates, lower survival rates, and smaller litter sizes, and many of the breeding lines died out. These results provide fundamental information about mouse genetics and reveal the impact of germline mutation rates on phenotypes in a mammalian population. |
format | Online Article Text |
id | pubmed-4509997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45099972016-01-31 Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice Uchimura, Arikuni Higuchi, Mayumi Minakuchi, Yohei Ohno, Mizuki Toyoda, Atsushi Fujiyama, Asao Miura, Ikuo Wakana, Shigeharu Nishino, Jo Yagi, Takeshi Genome Res Research The germline mutation rate is an important parameter that affects the amount of genetic variation and the rate of evolution. However, neither the rate of germline mutations in laboratory mice nor the biological significance of the mutation rate in mammalian populations is clear. Here we studied genome-wide mutation rates and the long-term effects of mutation accumulation on phenotype in more than 20 generations of wild-type C57BL/6 mice and mutator mice, which have high DNA replication error rates. We estimated the base-substitution mutation rate to be 5.4 × 10(−9) (95% confidence interval = 4.6 × 10(−9)–6.5 × 10(−9)) per nucleotide per generation in C57BL/6 laboratory mice, about half the rate reported in humans. The mutation rate in mutator mice was 17 times that in wild-type mice. Abnormal phenotypes were 4.1-fold more frequent in the mutator lines than in the wild-type lines. After several generations, the mutator mice reproduced at substantially lower rates than the controls, exhibiting low pregnancy rates, lower survival rates, and smaller litter sizes, and many of the breeding lines died out. These results provide fundamental information about mouse genetics and reveal the impact of germline mutation rates on phenotypes in a mammalian population. Cold Spring Harbor Laboratory Press 2015-08 /pmc/articles/PMC4509997/ /pubmed/26129709 http://dx.doi.org/10.1101/gr.186148.114 Text en © 2015 Uchimura et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Uchimura, Arikuni Higuchi, Mayumi Minakuchi, Yohei Ohno, Mizuki Toyoda, Atsushi Fujiyama, Asao Miura, Ikuo Wakana, Shigeharu Nishino, Jo Yagi, Takeshi Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
title | Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
title_full | Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
title_fullStr | Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
title_full_unstemmed | Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
title_short | Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
title_sort | germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4509997/ https://www.ncbi.nlm.nih.gov/pubmed/26129709 http://dx.doi.org/10.1101/gr.186148.114 |
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