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Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding
Vampire bats are the only mammals that feed exclusively on blood. To uncover genomic changes associated with this dietary adaptation, we generated a haplotype-resolved genome of the common vampire bat and screened 27 bat species for genes that were specifically lost in the vampire bat lineage. We fo...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956264/ https://www.ncbi.nlm.nih.gov/pubmed/35333583 http://dx.doi.org/10.1126/sciadv.abm6494 |
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author | Blumer, Moritz Brown, Tom Freitas, Mariella Bontempo Destro, Ana Luiza Oliveira, Juraci A. Morales, Ariadna E. Schell, Tilman Greve, Carola Pippel, Martin Jebb, David Hecker, Nikolai Ahmed, Alexis-Walid Kirilenko, Bogdan M. Foote, Maddy Janke, Axel Lim, Burton K. Hiller, Michael |
author_facet | Blumer, Moritz Brown, Tom Freitas, Mariella Bontempo Destro, Ana Luiza Oliveira, Juraci A. Morales, Ariadna E. Schell, Tilman Greve, Carola Pippel, Martin Jebb, David Hecker, Nikolai Ahmed, Alexis-Walid Kirilenko, Bogdan M. Foote, Maddy Janke, Axel Lim, Burton K. Hiller, Michael |
author_sort | Blumer, Moritz |
collection | PubMed |
description | Vampire bats are the only mammals that feed exclusively on blood. To uncover genomic changes associated with this dietary adaptation, we generated a haplotype-resolved genome of the common vampire bat and screened 27 bat species for genes that were specifically lost in the vampire bat lineage. We found previously unknown gene losses that relate to reduced insulin secretion (FFAR1 and SLC30A8), limited glycogen stores (PPP1R3E), and a unique gastric physiology (CTSE). Other gene losses likely reflect the biased nutrient composition (ERN2 and CTRL) and distinct pathogen diversity of blood (RNASE7) and predict the complete lack of cone-based vision in these strictly nocturnal bats (PDE6H and PDE6C). Notably, REP15 loss likely helped vampire bats adapt to high dietary iron levels by enhancing iron excretion, and the loss of CYP39A1 could have contributed to their exceptional cognitive abilities. These findings enhance our understanding of vampire bat biology and the genomic underpinnings of adaptations to blood feeding. |
format | Online Article Text |
id | pubmed-8956264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-89562642022-04-04 Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding Blumer, Moritz Brown, Tom Freitas, Mariella Bontempo Destro, Ana Luiza Oliveira, Juraci A. Morales, Ariadna E. Schell, Tilman Greve, Carola Pippel, Martin Jebb, David Hecker, Nikolai Ahmed, Alexis-Walid Kirilenko, Bogdan M. Foote, Maddy Janke, Axel Lim, Burton K. Hiller, Michael Sci Adv Biomedicine and Life Sciences Vampire bats are the only mammals that feed exclusively on blood. To uncover genomic changes associated with this dietary adaptation, we generated a haplotype-resolved genome of the common vampire bat and screened 27 bat species for genes that were specifically lost in the vampire bat lineage. We found previously unknown gene losses that relate to reduced insulin secretion (FFAR1 and SLC30A8), limited glycogen stores (PPP1R3E), and a unique gastric physiology (CTSE). Other gene losses likely reflect the biased nutrient composition (ERN2 and CTRL) and distinct pathogen diversity of blood (RNASE7) and predict the complete lack of cone-based vision in these strictly nocturnal bats (PDE6H and PDE6C). Notably, REP15 loss likely helped vampire bats adapt to high dietary iron levels by enhancing iron excretion, and the loss of CYP39A1 could have contributed to their exceptional cognitive abilities. These findings enhance our understanding of vampire bat biology and the genomic underpinnings of adaptations to blood feeding. American Association for the Advancement of Science 2022-03-25 /pmc/articles/PMC8956264/ /pubmed/35333583 http://dx.doi.org/10.1126/sciadv.abm6494 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Blumer, Moritz Brown, Tom Freitas, Mariella Bontempo Destro, Ana Luiza Oliveira, Juraci A. Morales, Ariadna E. Schell, Tilman Greve, Carola Pippel, Martin Jebb, David Hecker, Nikolai Ahmed, Alexis-Walid Kirilenko, Bogdan M. Foote, Maddy Janke, Axel Lim, Burton K. Hiller, Michael Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
title | Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
title_full | Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
title_fullStr | Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
title_full_unstemmed | Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
title_short | Gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
title_sort | gene losses in the common vampire bat illuminate molecular adaptations to blood feeding |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956264/ https://www.ncbi.nlm.nih.gov/pubmed/35333583 http://dx.doi.org/10.1126/sciadv.abm6494 |
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