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Analysis of Microsatellite Polymorphism in Inbred Knockout Mice
Previously, we found that the genotype of 42 out of 198 mouse microsatellite loci, which are distributed among all chromosomes except the Y chromosome, changed from monomorphism to polymorphism (CMP) in a genetically modified inbred mouse strain. In this study, we further examined whether CMP also r...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324499/ https://www.ncbi.nlm.nih.gov/pubmed/22509320 http://dx.doi.org/10.1371/journal.pone.0034555 |
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author | Zuo, Baofen Du, Xiaoyan Zhao, Jing Yang, Huixin Wang, Chao Wu, Yanhua Lu, Jing Wang, Ying Chen, Zhenwen |
author_facet | Zuo, Baofen Du, Xiaoyan Zhao, Jing Yang, Huixin Wang, Chao Wu, Yanhua Lu, Jing Wang, Ying Chen, Zhenwen |
author_sort | Zuo, Baofen |
collection | PubMed |
description | Previously, we found that the genotype of 42 out of 198 mouse microsatellite loci, which are distributed among all chromosomes except the Y chromosome, changed from monomorphism to polymorphism (CMP) in a genetically modified inbred mouse strain. In this study, we further examined whether CMP also relates to the homologous recombination in gene knockout (KO) mouse strains. The same 42 microsatellite loci were analyzed by polymerase chain reaction (PCR) in 29 KO inbred mouse strains via short tandem sequence repeat (STR) scanning and direct sequence cloning to justify microsatellite polymorphisms. The C57BL/6J and 129 mouse strains, from which these 29 KO mice were derived, were chosen as the background controls. The results indicated that 10 out of 42 (23.8%) loci showed CMP in some of these mouse strains. Except for the trinucleotide repeat locus of D3Mit22, which had microsatellite CMP in strain number 9, the core sequences of the remaining 41 loci were dinucleotide repeats, and 9 out of 41 (21.95%) showed CMPs among detected mouse strains. However, 11 out of 29 (37.9%) KO mice strains were recognized as having CMPs. The popular dinucleotide motifs in CMP were (TG)(n) (50%, 2/4), followed by (GT)(n) (27.27%, 3/11) and (CA)(n) (23.08%, 3/13). The microsatellite CMP in (CT)(n) and (AG)(n) repeats were 20% (1/5). According to cloning sequencing results, 6 KO mouse strains showed insertions of nucleotides whereas 1 showed a deletion. Furthermore, 2 loci (D13Mit3 and D14Mit102) revealed CMP in 2 strains, and mouse strain number 9 showed CMPs in two loci (D3Mit22 and D13Mit3) simultaneously. Collectively, these results indicated that microsatellite polymorphisms were present in the examined inbred KO mice. |
format | Online Article Text |
id | pubmed-3324499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33244992012-04-16 Analysis of Microsatellite Polymorphism in Inbred Knockout Mice Zuo, Baofen Du, Xiaoyan Zhao, Jing Yang, Huixin Wang, Chao Wu, Yanhua Lu, Jing Wang, Ying Chen, Zhenwen PLoS One Research Article Previously, we found that the genotype of 42 out of 198 mouse microsatellite loci, which are distributed among all chromosomes except the Y chromosome, changed from monomorphism to polymorphism (CMP) in a genetically modified inbred mouse strain. In this study, we further examined whether CMP also relates to the homologous recombination in gene knockout (KO) mouse strains. The same 42 microsatellite loci were analyzed by polymerase chain reaction (PCR) in 29 KO inbred mouse strains via short tandem sequence repeat (STR) scanning and direct sequence cloning to justify microsatellite polymorphisms. The C57BL/6J and 129 mouse strains, from which these 29 KO mice were derived, were chosen as the background controls. The results indicated that 10 out of 42 (23.8%) loci showed CMP in some of these mouse strains. Except for the trinucleotide repeat locus of D3Mit22, which had microsatellite CMP in strain number 9, the core sequences of the remaining 41 loci were dinucleotide repeats, and 9 out of 41 (21.95%) showed CMPs among detected mouse strains. However, 11 out of 29 (37.9%) KO mice strains were recognized as having CMPs. The popular dinucleotide motifs in CMP were (TG)(n) (50%, 2/4), followed by (GT)(n) (27.27%, 3/11) and (CA)(n) (23.08%, 3/13). The microsatellite CMP in (CT)(n) and (AG)(n) repeats were 20% (1/5). According to cloning sequencing results, 6 KO mouse strains showed insertions of nucleotides whereas 1 showed a deletion. Furthermore, 2 loci (D13Mit3 and D14Mit102) revealed CMP in 2 strains, and mouse strain number 9 showed CMPs in two loci (D3Mit22 and D13Mit3) simultaneously. Collectively, these results indicated that microsatellite polymorphisms were present in the examined inbred KO mice. Public Library of Science 2012-04-11 /pmc/articles/PMC3324499/ /pubmed/22509320 http://dx.doi.org/10.1371/journal.pone.0034555 Text en Zuo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zuo, Baofen Du, Xiaoyan Zhao, Jing Yang, Huixin Wang, Chao Wu, Yanhua Lu, Jing Wang, Ying Chen, Zhenwen Analysis of Microsatellite Polymorphism in Inbred Knockout Mice |
title | Analysis of Microsatellite Polymorphism in Inbred Knockout Mice |
title_full | Analysis of Microsatellite Polymorphism in Inbred Knockout Mice |
title_fullStr | Analysis of Microsatellite Polymorphism in Inbred Knockout Mice |
title_full_unstemmed | Analysis of Microsatellite Polymorphism in Inbred Knockout Mice |
title_short | Analysis of Microsatellite Polymorphism in Inbred Knockout Mice |
title_sort | analysis of microsatellite polymorphism in inbred knockout mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3324499/ https://www.ncbi.nlm.nih.gov/pubmed/22509320 http://dx.doi.org/10.1371/journal.pone.0034555 |
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