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Mouse protein coding diversity: What’s left to discover?
For over a century, mice have been used to model human disease, leading to many fundamental discoveries about mammalian biology and the development of new therapies. Mouse genetics research has been further catalysed by a plethora of genomic resources developed in the last 20 years, including the ge...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855407/ https://www.ncbi.nlm.nih.gov/pubmed/31725724 http://dx.doi.org/10.1371/journal.pgen.1008446 |
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author | Lilue, Jingtao Shivalikanjli, Anu Adams, David J. Keane, Thomas M. |
author_facet | Lilue, Jingtao Shivalikanjli, Anu Adams, David J. Keane, Thomas M. |
author_sort | Lilue, Jingtao |
collection | PubMed |
description | For over a century, mice have been used to model human disease, leading to many fundamental discoveries about mammalian biology and the development of new therapies. Mouse genetics research has been further catalysed by a plethora of genomic resources developed in the last 20 years, including the genome sequence of C57BL/6J and more recently the first draft reference genomes for 16 additional laboratory strains. Collectively, the comparison of these genomes highlights the extreme diversity that exists at loci associated with the immune system, pathogen response, and key sensory functions, which form the foundation for dissecting phenotypic traits in vivo. We review the current status of the mouse genome across the diversity of the mouse lineage and discuss the value of mice to understanding human disease. |
format | Online Article Text |
id | pubmed-6855407 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-68554072019-11-22 Mouse protein coding diversity: What’s left to discover? Lilue, Jingtao Shivalikanjli, Anu Adams, David J. Keane, Thomas M. PLoS Genet Review For over a century, mice have been used to model human disease, leading to many fundamental discoveries about mammalian biology and the development of new therapies. Mouse genetics research has been further catalysed by a plethora of genomic resources developed in the last 20 years, including the genome sequence of C57BL/6J and more recently the first draft reference genomes for 16 additional laboratory strains. Collectively, the comparison of these genomes highlights the extreme diversity that exists at loci associated with the immune system, pathogen response, and key sensory functions, which form the foundation for dissecting phenotypic traits in vivo. We review the current status of the mouse genome across the diversity of the mouse lineage and discuss the value of mice to understanding human disease. Public Library of Science 2019-11-14 /pmc/articles/PMC6855407/ /pubmed/31725724 http://dx.doi.org/10.1371/journal.pgen.1008446 Text en © 2019 Lilue 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Lilue, Jingtao Shivalikanjli, Anu Adams, David J. Keane, Thomas M. Mouse protein coding diversity: What’s left to discover? |
title | Mouse protein coding diversity: What’s left to discover? |
title_full | Mouse protein coding diversity: What’s left to discover? |
title_fullStr | Mouse protein coding diversity: What’s left to discover? |
title_full_unstemmed | Mouse protein coding diversity: What’s left to discover? |
title_short | Mouse protein coding diversity: What’s left to discover? |
title_sort | mouse protein coding diversity: what’s left to discover? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6855407/ https://www.ncbi.nlm.nih.gov/pubmed/31725724 http://dx.doi.org/10.1371/journal.pgen.1008446 |
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