Cargando…
The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures
BACKGROUND: The cinereous vulture, Aegypius monachus, is the largest bird of prey and plays a key role in the ecosystem by removing carcasses, thus preventing the spread of diseases. Its feeding habits force it to cope with constant exposure to pathogens, making this species an interesting target fo...
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618389/ https://www.ncbi.nlm.nih.gov/pubmed/26486310 http://dx.doi.org/10.1186/s13059-015-0780-4 |
_version_ | 1782396916312571904 |
---|---|
author | Chung, Oksung Jin, Seondeok Cho, Yun Sung Lim, Jeongheui Kim, Hyunho Jho, Sungwoong Kim, Hak-Min Jun, JeHoon Lee, HyeJin Chon, Alvin Ko, Junsu Edwards, Jeremy Weber, Jessica A. Han, Kyudong O’Brien, Stephen J. Manica, Andrea Bhak, Jong Paek, Woon Kee |
author_facet | Chung, Oksung Jin, Seondeok Cho, Yun Sung Lim, Jeongheui Kim, Hyunho Jho, Sungwoong Kim, Hak-Min Jun, JeHoon Lee, HyeJin Chon, Alvin Ko, Junsu Edwards, Jeremy Weber, Jessica A. Han, Kyudong O’Brien, Stephen J. Manica, Andrea Bhak, Jong Paek, Woon Kee |
author_sort | Chung, Oksung |
collection | PubMed |
description | BACKGROUND: The cinereous vulture, Aegypius monachus, is the largest bird of prey and plays a key role in the ecosystem by removing carcasses, thus preventing the spread of diseases. Its feeding habits force it to cope with constant exposure to pathogens, making this species an interesting target for discovering functionally selected genetic variants. Furthermore, the presence of two independently evolved vulture groups, Old World and New World vultures, provides a natural experiment in which to investigate convergent evolution due to obligate scavenging. RESULTS: We sequenced the genome of a cinereous vulture, and mapped it to the bald eagle reference genome, a close relative with a divergence time of 18 million years. By comparing the cinereous vulture to other avian genomes, we find positively selected genetic variations in this species associated with respiration, likely linked to their ability of immune defense responses and gastric acid secretion, consistent with their ability to digest carcasses. Comparisons between the Old World and New World vulture groups suggest convergent gene evolution. We assemble the cinereous vulture blood transcriptome from a second individual, and annotate genes. Finally, we infer the demographic history of the cinereous vulture which shows marked fluctuations in effective population size during the late Pleistocene. CONCLUSIONS: We present the first genome and transcriptome analyses of the cinereous vulture compared to other avian genomes and transcriptomes, revealing genetic signatures of dietary and environmental adaptations accompanied by possible convergent evolution between the Old World and New World vultures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0780-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4618389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46183892015-10-25 The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures Chung, Oksung Jin, Seondeok Cho, Yun Sung Lim, Jeongheui Kim, Hyunho Jho, Sungwoong Kim, Hak-Min Jun, JeHoon Lee, HyeJin Chon, Alvin Ko, Junsu Edwards, Jeremy Weber, Jessica A. Han, Kyudong O’Brien, Stephen J. Manica, Andrea Bhak, Jong Paek, Woon Kee Genome Biol Research BACKGROUND: The cinereous vulture, Aegypius monachus, is the largest bird of prey and plays a key role in the ecosystem by removing carcasses, thus preventing the spread of diseases. Its feeding habits force it to cope with constant exposure to pathogens, making this species an interesting target for discovering functionally selected genetic variants. Furthermore, the presence of two independently evolved vulture groups, Old World and New World vultures, provides a natural experiment in which to investigate convergent evolution due to obligate scavenging. RESULTS: We sequenced the genome of a cinereous vulture, and mapped it to the bald eagle reference genome, a close relative with a divergence time of 18 million years. By comparing the cinereous vulture to other avian genomes, we find positively selected genetic variations in this species associated with respiration, likely linked to their ability of immune defense responses and gastric acid secretion, consistent with their ability to digest carcasses. Comparisons between the Old World and New World vulture groups suggest convergent gene evolution. We assemble the cinereous vulture blood transcriptome from a second individual, and annotate genes. Finally, we infer the demographic history of the cinereous vulture which shows marked fluctuations in effective population size during the late Pleistocene. CONCLUSIONS: We present the first genome and transcriptome analyses of the cinereous vulture compared to other avian genomes and transcriptomes, revealing genetic signatures of dietary and environmental adaptations accompanied by possible convergent evolution between the Old World and New World vultures. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0780-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-21 2015 /pmc/articles/PMC4618389/ /pubmed/26486310 http://dx.doi.org/10.1186/s13059-015-0780-4 Text en © Chung et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chung, Oksung Jin, Seondeok Cho, Yun Sung Lim, Jeongheui Kim, Hyunho Jho, Sungwoong Kim, Hak-Min Jun, JeHoon Lee, HyeJin Chon, Alvin Ko, Junsu Edwards, Jeremy Weber, Jessica A. Han, Kyudong O’Brien, Stephen J. Manica, Andrea Bhak, Jong Paek, Woon Kee The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures |
title | The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures |
title_full | The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures |
title_fullStr | The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures |
title_full_unstemmed | The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures |
title_short | The first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the Old and New World vultures |
title_sort | first whole genome and transcriptome of the cinereous vulture reveals adaptation in the gastric and immune defense systems and possible convergent evolution between the old and new world vultures |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618389/ https://www.ncbi.nlm.nih.gov/pubmed/26486310 http://dx.doi.org/10.1186/s13059-015-0780-4 |
work_keys_str_mv | AT chungoksung thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT jinseondeok thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT choyunsung thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT limjeongheui thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT kimhyunho thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT jhosungwoong thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT kimhakmin thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT junjehoon thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT leehyejin thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT chonalvin thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT kojunsu thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT edwardsjeremy thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT weberjessicaa thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT hankyudong thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT obrienstephenj thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT manicaandrea thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT bhakjong thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT paekwoonkee thefirstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT chungoksung firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT jinseondeok firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT choyunsung firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT limjeongheui firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT kimhyunho firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT jhosungwoong firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT kimhakmin firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT junjehoon firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT leehyejin firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT chonalvin firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT kojunsu firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT edwardsjeremy firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT weberjessicaa firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT hankyudong firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT obrienstephenj firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT manicaandrea firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT bhakjong firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures AT paekwoonkee firstwholegenomeandtranscriptomeofthecinereousvulturerevealsadaptationinthegastricandimmunedefensesystemsandpossibleconvergentevolutionbetweentheoldandnewworldvultures |