Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/21298
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dc.contributor.authorSisu, C-
dc.contributor.authorMuir, P-
dc.contributor.authorFrankish, A-
dc.contributor.authorFiddes, I-
dc.contributor.authorDiekhans, M-
dc.contributor.authorThybert, D-
dc.contributor.authorOdom, DT-
dc.contributor.authorFlicek, P-
dc.contributor.authorKeane, T-
dc.contributor.authorHubbard, T-
dc.contributor.authorHarrow, J-
dc.contributor.authorGerstein, M-
dc.date.accessioned2020-07-29T08:54:13Z-
dc.date.available2020-07-29T08:54:13Z-
dc.date.issued2020-07-29-
dc.identifier3695-
dc.identifier.citationSisu, C., Muir, P., Frankish, A. et al. (2020) 'Transcriptional activity and strain-specific history of mouse pseudogenes', Nature Communications, 11, 3695, pp. 1-14. doi: 10.1038/s41467-020-17157-w.en_US
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/21298-
dc.description.abstractCopyright © The Author(s) 2020. 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.-
dc.description.sponsorshipThis project was supported by the Wellcome Trust (grant numbers WT108749/Z/15/Z, WT098051, WT202878/Z/16/Z and WT202878/B/16/Z), Cancer Research UK (20412), the European Research Council (615584), the European Molecular Biology Laboratory, and the National Human Genome Research Institute of the National Institutes of Health under Award Number U41HG007234. The research leading to these results has received funding from the European Union’s Seventh Framework Programme (FP7/2007- 2013) under grant agreement HEALTH-F4-2010-241504 (EURATRANS).en_US
dc.format.extent1 - 14-
dc.format.mediumElectronic-
dc.language.isoenen_US
dc.publisherNature Researchen_US
dc.rightsCopyright © 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 https://creativecommons.org/licenses/by/4.0/.-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.titleTranscriptional activity and strain-specific history of mouse pseudogenesen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1038/s41467-020-17157-w-
dc.relation.isPartOfNature Communications-
pubs.publication-statusPublished-
pubs.volume11-
dc.identifier.eissn2041-1723-
Appears in Collections:Dept of Life Sciences Research Papers

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