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Transcriptional activity and strain-specific history of mouse pseudogenes
Pseudogenes are ideal markers of genome remodelling. In turn, the mouse is an ideal platform for studying them, particularly with the recent availability of strain-sequencing and transcriptional data. Here, combining both manual curation and automatic pipelines, we present a genome-wide annotation o...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392758/ https://www.ncbi.nlm.nih.gov/pubmed/32728065 http://dx.doi.org/10.1038/s41467-020-17157-w |
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author | Sisu, Cristina Muir, Paul Frankish, Adam Fiddes, Ian Diekhans, Mark Thybert, David Odom, Duncan T. Flicek, Paul Keane, Thomas M. Hubbard, Tim Harrow, Jennifer Gerstein, Mark |
author_facet | Sisu, Cristina Muir, Paul Frankish, Adam Fiddes, Ian Diekhans, Mark Thybert, David Odom, Duncan T. Flicek, Paul Keane, Thomas M. Hubbard, Tim Harrow, Jennifer Gerstein, Mark |
author_sort | Sisu, Cristina |
collection | PubMed |
description | Pseudogenes are ideal markers of genome remodelling. In turn, the mouse is an ideal platform for studying them, particularly with the recent availability of strain-sequencing and transcriptional data. Here, combining both manual curation and automatic pipelines, we present a genome-wide annotation of the pseudogenes in the mouse reference genome and 18 inbred mouse strains (available via the mouse.pseudogene.org resource). We also annotate 165 unitary pseudogenes in mouse, and 303, in human. The overall pseudogene repertoire in mouse is similar to that in human in terms of size, biotype distribution, and family composition (e.g. with GAPDH and ribosomal proteins being the largest families). Notable differences arise in the pseudogene age distribution, with multiple retro-transpositional bursts in mouse evolutionary history and only one in human. Furthermore, in each strain about a fifth of all pseudogenes are unique, reflecting strain-specific evolution. Finally, we find that ~15% of the mouse pseudogenes are transcribed, and that highly transcribed parent genes tend to give rise to many processed pseudogenes. |
format | Online Article Text |
id | pubmed-7392758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73927582020-08-12 Transcriptional activity and strain-specific history of mouse pseudogenes Sisu, Cristina Muir, Paul Frankish, Adam Fiddes, Ian Diekhans, Mark Thybert, David Odom, Duncan T. Flicek, Paul Keane, Thomas M. Hubbard, Tim Harrow, Jennifer Gerstein, Mark Nat Commun Article Pseudogenes are ideal markers of genome remodelling. In turn, the mouse is an ideal platform for studying them, particularly with the recent availability of strain-sequencing and transcriptional data. Here, combining both manual curation and automatic pipelines, we present a genome-wide annotation of the pseudogenes in the mouse reference genome and 18 inbred mouse strains (available via the mouse.pseudogene.org resource). We also annotate 165 unitary pseudogenes in mouse, and 303, in human. The overall pseudogene repertoire in mouse is similar to that in human in terms of size, biotype distribution, and family composition (e.g. with GAPDH and ribosomal proteins being the largest families). Notable differences arise in the pseudogene age distribution, with multiple retro-transpositional bursts in mouse evolutionary history and only one in human. Furthermore, in each strain about a fifth of all pseudogenes are unique, reflecting strain-specific evolution. Finally, we find that ~15% of the mouse pseudogenes are transcribed, and that highly transcribed parent genes tend to give rise to many processed pseudogenes. Nature Publishing Group UK 2020-07-29 /pmc/articles/PMC7392758/ /pubmed/32728065 http://dx.doi.org/10.1038/s41467-020-17157-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Sisu, Cristina Muir, Paul Frankish, Adam Fiddes, Ian Diekhans, Mark Thybert, David Odom, Duncan T. Flicek, Paul Keane, Thomas M. Hubbard, Tim Harrow, Jennifer Gerstein, Mark Transcriptional activity and strain-specific history of mouse pseudogenes |
title | Transcriptional activity and strain-specific history of mouse pseudogenes |
title_full | Transcriptional activity and strain-specific history of mouse pseudogenes |
title_fullStr | Transcriptional activity and strain-specific history of mouse pseudogenes |
title_full_unstemmed | Transcriptional activity and strain-specific history of mouse pseudogenes |
title_short | Transcriptional activity and strain-specific history of mouse pseudogenes |
title_sort | transcriptional activity and strain-specific history of mouse pseudogenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7392758/ https://www.ncbi.nlm.nih.gov/pubmed/32728065 http://dx.doi.org/10.1038/s41467-020-17157-w |
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