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Genome sequencing and application of Taiwanese macaque Macaca cyclopis
Formosan macaque (Macaca cyclopis) is the only non-human primate in Taiwan Island. We performed de novo hybrid assembly for M. cyclopis using Illumina paired-end short reads, mate-pair reads and Nanopore long reads and obtained 5065 contigs with a N50 of 2.66 megabases. M. cyclopis contigs > = 1...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352370/ https://www.ncbi.nlm.nih.gov/pubmed/37460589 http://dx.doi.org/10.1038/s41598-023-38402-4 |
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author | Chiu, Kuo-Ping Stuart, Lutimba Ooi, Hong Sain Yu, John Smith, David Glenn Pei, Kurtis Jai-Chyi |
author_facet | Chiu, Kuo-Ping Stuart, Lutimba Ooi, Hong Sain Yu, John Smith, David Glenn Pei, Kurtis Jai-Chyi |
author_sort | Chiu, Kuo-Ping |
collection | PubMed |
description | Formosan macaque (Macaca cyclopis) is the only non-human primate in Taiwan Island. We performed de novo hybrid assembly for M. cyclopis using Illumina paired-end short reads, mate-pair reads and Nanopore long reads and obtained 5065 contigs with a N50 of 2.66 megabases. M. cyclopis contigs > = 10 kb were assigned to chromosomes using Indian rhesus macaque (Macaca mulatta mulatta) genome assembly Mmul_10 as reference, resulting in a draft of M. cyclopis genome of 2,846,042,475 bases, distributed in 21 chromosomes. The draft genome contains 23,462 transcriptional origins (genes), capable of expressing 716,231 exons in 59,484 transcripts. Genome-based phylogenetic study using the assembled M. cyclopis genome together with genomes of four other macaque species, human, orangutan and chimpanzee showed similar result as previously reported. However, the M. cyclopis species was found to diverge from Chinese M. mulatta lasiota about 1.8 million years ago. Fossil gene analysis detected the presence of gap and pol endogenous viral elements of simian retrovirus in all macaques tested, including M. fascicularis, M. m. mulatta and M. cyclopis. However, M. cyclopis showed ~ 2 times less in number and more uniform in chromosomal locations. The constrain in foreign genome disturbance, presumably due to geographical isolation, should be able to simplify genomics-related investigations, making M. cyclopis an ideal primate species for medical research. |
format | Online Article Text |
id | pubmed-10352370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103523702023-07-19 Genome sequencing and application of Taiwanese macaque Macaca cyclopis Chiu, Kuo-Ping Stuart, Lutimba Ooi, Hong Sain Yu, John Smith, David Glenn Pei, Kurtis Jai-Chyi Sci Rep Article Formosan macaque (Macaca cyclopis) is the only non-human primate in Taiwan Island. We performed de novo hybrid assembly for M. cyclopis using Illumina paired-end short reads, mate-pair reads and Nanopore long reads and obtained 5065 contigs with a N50 of 2.66 megabases. M. cyclopis contigs > = 10 kb were assigned to chromosomes using Indian rhesus macaque (Macaca mulatta mulatta) genome assembly Mmul_10 as reference, resulting in a draft of M. cyclopis genome of 2,846,042,475 bases, distributed in 21 chromosomes. The draft genome contains 23,462 transcriptional origins (genes), capable of expressing 716,231 exons in 59,484 transcripts. Genome-based phylogenetic study using the assembled M. cyclopis genome together with genomes of four other macaque species, human, orangutan and chimpanzee showed similar result as previously reported. However, the M. cyclopis species was found to diverge from Chinese M. mulatta lasiota about 1.8 million years ago. Fossil gene analysis detected the presence of gap and pol endogenous viral elements of simian retrovirus in all macaques tested, including M. fascicularis, M. m. mulatta and M. cyclopis. However, M. cyclopis showed ~ 2 times less in number and more uniform in chromosomal locations. The constrain in foreign genome disturbance, presumably due to geographical isolation, should be able to simplify genomics-related investigations, making M. cyclopis an ideal primate species for medical research. Nature Publishing Group UK 2023-07-17 /pmc/articles/PMC10352370/ /pubmed/37460589 http://dx.doi.org/10.1038/s41598-023-38402-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 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/) . |
spellingShingle | Article Chiu, Kuo-Ping Stuart, Lutimba Ooi, Hong Sain Yu, John Smith, David Glenn Pei, Kurtis Jai-Chyi Genome sequencing and application of Taiwanese macaque Macaca cyclopis |
title | Genome sequencing and application of Taiwanese macaque Macaca cyclopis |
title_full | Genome sequencing and application of Taiwanese macaque Macaca cyclopis |
title_fullStr | Genome sequencing and application of Taiwanese macaque Macaca cyclopis |
title_full_unstemmed | Genome sequencing and application of Taiwanese macaque Macaca cyclopis |
title_short | Genome sequencing and application of Taiwanese macaque Macaca cyclopis |
title_sort | genome sequencing and application of taiwanese macaque macaca cyclopis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352370/ https://www.ncbi.nlm.nih.gov/pubmed/37460589 http://dx.doi.org/10.1038/s41598-023-38402-4 |
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