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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
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.
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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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