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Six reference-quality genomes reveal evolution of bat adaptations
Bats possess extraordinary adaptations, including flight, echolocation, extreme longevity and unique immunity. High-quality genomes are crucial for understanding the molecular basis and evolution of these traits. Here we incorporated long-read sequencing and state-of-the-art scaffolding protocols(1)...
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/PMC8075899/ https://www.ncbi.nlm.nih.gov/pubmed/32699395 http://dx.doi.org/10.1038/s41586-020-2486-3 |
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author | Jebb, David Huang, Zixia Pippel, Martin Hughes, Graham M. Lavrichenko, Ksenia Devanna, Paolo Winkler, Sylke Jermiin, Lars S. Skirmuntt, Emilia C. Katzourakis, Aris Burkitt-Gray, Lucy Ray, David A. Sullivan, Kevin A. M. Roscito, Juliana G. Kirilenko, Bogdan M. Dávalos, Liliana M. Corthals, Angelique P. Power, Megan L. Jones, Gareth Ransome, Roger D. Dechmann, Dina K. N. Locatelli, Andrea G. Puechmaille, Sébastien J. Fedrigo, Olivier Jarvis, Erich D. Hiller, Michael Vernes, Sonja C. Myers, Eugene W. Teeling, Emma C. |
author_facet | Jebb, David Huang, Zixia Pippel, Martin Hughes, Graham M. Lavrichenko, Ksenia Devanna, Paolo Winkler, Sylke Jermiin, Lars S. Skirmuntt, Emilia C. Katzourakis, Aris Burkitt-Gray, Lucy Ray, David A. Sullivan, Kevin A. M. Roscito, Juliana G. Kirilenko, Bogdan M. Dávalos, Liliana M. Corthals, Angelique P. Power, Megan L. Jones, Gareth Ransome, Roger D. Dechmann, Dina K. N. Locatelli, Andrea G. Puechmaille, Sébastien J. Fedrigo, Olivier Jarvis, Erich D. Hiller, Michael Vernes, Sonja C. Myers, Eugene W. Teeling, Emma C. |
author_sort | Jebb, David |
collection | PubMed |
description | Bats possess extraordinary adaptations, including flight, echolocation, extreme longevity and unique immunity. High-quality genomes are crucial for understanding the molecular basis and evolution of these traits. Here we incorporated long-read sequencing and state-of-the-art scaffolding protocols(1) to generate, to our knowledge, the first reference-quality genomes of six bat species (Rhinolophus ferrumequinum, Rousettus aegyptiacus, Phyllostomus discolor, Myotis myotis, Pipistrellus kuhlii and Molossus molossus). We integrated gene projections from our ‘Tool to infer Orthologs from Genome Alignments’ (TOGA) software with de novo and homology gene predictions as well as short- and long-read transcriptomics to generate highly complete gene annotations. To resolve the phylogenetic position of bats within Laurasiatheria, we applied several phylogenetic methods to comprehensive sets of orthologous protein-coding and noncoding regions of the genome, and identified a basal origin for bats within Scrotifera. Our genome-wide screens revealed positive selection on hearing-related genes in the ancestral branch of bats, which is indicative of laryngeal echolocation being an ancestral trait in this clade. We found selection and loss of immunity-related genes (including pro-inflammatory NF-κB regulators) and expansions of anti-viral APOBEC3 genes, which highlights molecular mechanisms that may contribute to the exceptional immunity of bats. Genomic integrations of diverse viruses provide a genomic record of historical tolerance to viral infection in bats. Finally, we found and experimentally validated bat-specific variation in microRNAs, which may regulate bat-specific gene-expression programs. Our reference-quality bat genomes provide the resources required to uncover and validate the genomic basis of adaptations of bats, and stimulate new avenues of research that are directly relevant to human health and disease(1). |
format | Online Article Text |
id | pubmed-8075899 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80758992021-05-06 Six reference-quality genomes reveal evolution of bat adaptations Jebb, David Huang, Zixia Pippel, Martin Hughes, Graham M. Lavrichenko, Ksenia Devanna, Paolo Winkler, Sylke Jermiin, Lars S. Skirmuntt, Emilia C. Katzourakis, Aris Burkitt-Gray, Lucy Ray, David A. Sullivan, Kevin A. M. Roscito, Juliana G. Kirilenko, Bogdan M. Dávalos, Liliana M. Corthals, Angelique P. Power, Megan L. Jones, Gareth Ransome, Roger D. Dechmann, Dina K. N. Locatelli, Andrea G. Puechmaille, Sébastien J. Fedrigo, Olivier Jarvis, Erich D. Hiller, Michael Vernes, Sonja C. Myers, Eugene W. Teeling, Emma C. Nature Article Bats possess extraordinary adaptations, including flight, echolocation, extreme longevity and unique immunity. High-quality genomes are crucial for understanding the molecular basis and evolution of these traits. Here we incorporated long-read sequencing and state-of-the-art scaffolding protocols(1) to generate, to our knowledge, the first reference-quality genomes of six bat species (Rhinolophus ferrumequinum, Rousettus aegyptiacus, Phyllostomus discolor, Myotis myotis, Pipistrellus kuhlii and Molossus molossus). We integrated gene projections from our ‘Tool to infer Orthologs from Genome Alignments’ (TOGA) software with de novo and homology gene predictions as well as short- and long-read transcriptomics to generate highly complete gene annotations. To resolve the phylogenetic position of bats within Laurasiatheria, we applied several phylogenetic methods to comprehensive sets of orthologous protein-coding and noncoding regions of the genome, and identified a basal origin for bats within Scrotifera. Our genome-wide screens revealed positive selection on hearing-related genes in the ancestral branch of bats, which is indicative of laryngeal echolocation being an ancestral trait in this clade. We found selection and loss of immunity-related genes (including pro-inflammatory NF-κB regulators) and expansions of anti-viral APOBEC3 genes, which highlights molecular mechanisms that may contribute to the exceptional immunity of bats. Genomic integrations of diverse viruses provide a genomic record of historical tolerance to viral infection in bats. Finally, we found and experimentally validated bat-specific variation in microRNAs, which may regulate bat-specific gene-expression programs. Our reference-quality bat genomes provide the resources required to uncover and validate the genomic basis of adaptations of bats, and stimulate new avenues of research that are directly relevant to human health and disease(1). Nature Publishing Group UK 2020-07-22 2020 /pmc/articles/PMC8075899/ /pubmed/32699395 http://dx.doi.org/10.1038/s41586-020-2486-3 Text en © The Author(s) 2020 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jebb, David Huang, Zixia Pippel, Martin Hughes, Graham M. Lavrichenko, Ksenia Devanna, Paolo Winkler, Sylke Jermiin, Lars S. Skirmuntt, Emilia C. Katzourakis, Aris Burkitt-Gray, Lucy Ray, David A. Sullivan, Kevin A. M. Roscito, Juliana G. Kirilenko, Bogdan M. Dávalos, Liliana M. Corthals, Angelique P. Power, Megan L. Jones, Gareth Ransome, Roger D. Dechmann, Dina K. N. Locatelli, Andrea G. Puechmaille, Sébastien J. Fedrigo, Olivier Jarvis, Erich D. Hiller, Michael Vernes, Sonja C. Myers, Eugene W. Teeling, Emma C. Six reference-quality genomes reveal evolution of bat adaptations |
title | Six reference-quality genomes reveal evolution of bat adaptations |
title_full | Six reference-quality genomes reveal evolution of bat adaptations |
title_fullStr | Six reference-quality genomes reveal evolution of bat adaptations |
title_full_unstemmed | Six reference-quality genomes reveal evolution of bat adaptations |
title_short | Six reference-quality genomes reveal evolution of bat adaptations |
title_sort | six reference-quality genomes reveal evolution of bat adaptations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8075899/ https://www.ncbi.nlm.nih.gov/pubmed/32699395 http://dx.doi.org/10.1038/s41586-020-2486-3 |
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