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A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes
BACKGROUND: The Nile rat (Avicanthis niloticus) is an important animal model because of its robust diurnal rhythm, a cone-rich retina, and a propensity to develop diet-induced diabetes without chemical or genetic modifications. A closer similarity to humans in these aspects, compared to the widely u...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641963/ https://www.ncbi.nlm.nih.gov/pubmed/36344967 http://dx.doi.org/10.1186/s12915-022-01427-8 |
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author | Toh, Huishi Yang, Chentao Formenti, Giulio Raja, Kalpana Yan, Lily Tracey, Alan Chow, William Howe, Kerstin Bergeron, Lucie A. Zhang, Guojie Haase, Bettina Mountcastle, Jacquelyn Fedrigo, Olivier Fogg, John Kirilenko, Bogdan Munegowda, Chetan Hiller, Michael Jain, Aashish Kihara, Daisuke Rhie, Arang Phillippy, Adam M. Swanson, Scott A. Jiang, Peng Clegg, Dennis O. Jarvis, Erich D. Thomson, James A. Stewart, Ron Chaisson, Mark J. P. Bukhman, Yury V. |
author_facet | Toh, Huishi Yang, Chentao Formenti, Giulio Raja, Kalpana Yan, Lily Tracey, Alan Chow, William Howe, Kerstin Bergeron, Lucie A. Zhang, Guojie Haase, Bettina Mountcastle, Jacquelyn Fedrigo, Olivier Fogg, John Kirilenko, Bogdan Munegowda, Chetan Hiller, Michael Jain, Aashish Kihara, Daisuke Rhie, Arang Phillippy, Adam M. Swanson, Scott A. Jiang, Peng Clegg, Dennis O. Jarvis, Erich D. Thomson, James A. Stewart, Ron Chaisson, Mark J. P. Bukhman, Yury V. |
author_sort | Toh, Huishi |
collection | PubMed |
description | BACKGROUND: The Nile rat (Avicanthis niloticus) is an important animal model because of its robust diurnal rhythm, a cone-rich retina, and a propensity to develop diet-induced diabetes without chemical or genetic modifications. A closer similarity to humans in these aspects, compared to the widely used Mus musculus and Rattus norvegicus models, holds the promise of better translation of research findings to the clinic. RESULTS: We report a 2.5 Gb, chromosome-level reference genome assembly with fully resolved parental haplotypes, generated with the Vertebrate Genomes Project (VGP). The assembly is highly contiguous, with contig N50 of 11.1 Mb, scaffold N50 of 83 Mb, and 95.2% of the sequence assigned to chromosomes. We used a novel workflow to identify 3613 segmental duplications and quantify duplicated genes. Comparative analyses revealed unique genomic features of the Nile rat, including some that affect genes associated with type 2 diabetes and metabolic dysfunctions. We discuss 14 genes that are heterozygous in the Nile rat or highly diverged from the house mouse. CONCLUSIONS: Our findings reflect the exceptional level of genomic resolution present in this assembly, which will greatly expand the potential of the Nile rat as a model organism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01427-8. |
format | Online Article Text |
id | pubmed-9641963 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96419632022-11-15 A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes Toh, Huishi Yang, Chentao Formenti, Giulio Raja, Kalpana Yan, Lily Tracey, Alan Chow, William Howe, Kerstin Bergeron, Lucie A. Zhang, Guojie Haase, Bettina Mountcastle, Jacquelyn Fedrigo, Olivier Fogg, John Kirilenko, Bogdan Munegowda, Chetan Hiller, Michael Jain, Aashish Kihara, Daisuke Rhie, Arang Phillippy, Adam M. Swanson, Scott A. Jiang, Peng Clegg, Dennis O. Jarvis, Erich D. Thomson, James A. Stewart, Ron Chaisson, Mark J. P. Bukhman, Yury V. BMC Biol Research Article BACKGROUND: The Nile rat (Avicanthis niloticus) is an important animal model because of its robust diurnal rhythm, a cone-rich retina, and a propensity to develop diet-induced diabetes without chemical or genetic modifications. A closer similarity to humans in these aspects, compared to the widely used Mus musculus and Rattus norvegicus models, holds the promise of better translation of research findings to the clinic. RESULTS: We report a 2.5 Gb, chromosome-level reference genome assembly with fully resolved parental haplotypes, generated with the Vertebrate Genomes Project (VGP). The assembly is highly contiguous, with contig N50 of 11.1 Mb, scaffold N50 of 83 Mb, and 95.2% of the sequence assigned to chromosomes. We used a novel workflow to identify 3613 segmental duplications and quantify duplicated genes. Comparative analyses revealed unique genomic features of the Nile rat, including some that affect genes associated with type 2 diabetes and metabolic dysfunctions. We discuss 14 genes that are heterozygous in the Nile rat or highly diverged from the house mouse. CONCLUSIONS: Our findings reflect the exceptional level of genomic resolution present in this assembly, which will greatly expand the potential of the Nile rat as a model organism. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-022-01427-8. BioMed Central 2022-11-08 /pmc/articles/PMC9641963/ /pubmed/36344967 http://dx.doi.org/10.1186/s12915-022-01427-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Toh, Huishi Yang, Chentao Formenti, Giulio Raja, Kalpana Yan, Lily Tracey, Alan Chow, William Howe, Kerstin Bergeron, Lucie A. Zhang, Guojie Haase, Bettina Mountcastle, Jacquelyn Fedrigo, Olivier Fogg, John Kirilenko, Bogdan Munegowda, Chetan Hiller, Michael Jain, Aashish Kihara, Daisuke Rhie, Arang Phillippy, Adam M. Swanson, Scott A. Jiang, Peng Clegg, Dennis O. Jarvis, Erich D. Thomson, James A. Stewart, Ron Chaisson, Mark J. P. Bukhman, Yury V. A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes |
title | A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes |
title_full | A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes |
title_fullStr | A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes |
title_full_unstemmed | A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes |
title_short | A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes |
title_sort | haplotype-resolved genome assembly of the nile rat facilitates exploration of the genetic basis of diabetes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641963/ https://www.ncbi.nlm.nih.gov/pubmed/36344967 http://dx.doi.org/10.1186/s12915-022-01427-8 |
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