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Kiwi genome provides insights into evolution of a nocturnal lifestyle

BACKGROUND: Kiwi, comprising five species from the genus Apteryx, are endangered, ground-dwelling bird species endemic to New Zealand. They are the smallest and only nocturnal representatives of the ratites. The timing of kiwi adaptation to a nocturnal niche and the genomic innovations, which shaped...

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Autores principales: Le Duc, Diana, Renaud, Gabriel, Krishnan, Arunkumar, Almén, Markus Sällman, Huynen, Leon, Prohaska, Sonja J., Ongyerth, Matthias, Bitarello, Bárbara D., Schiöth, Helgi B., Hofreiter, Michael, Stadler, Peter F., Prüfer, Kay, Lambert, David, Kelso, Janet, Schöneberg, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511969/
https://www.ncbi.nlm.nih.gov/pubmed/26201466
http://dx.doi.org/10.1186/s13059-015-0711-4
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author Le Duc, Diana
Renaud, Gabriel
Krishnan, Arunkumar
Almén, Markus Sällman
Huynen, Leon
Prohaska, Sonja J.
Ongyerth, Matthias
Bitarello, Bárbara D.
Schiöth, Helgi B.
Hofreiter, Michael
Stadler, Peter F.
Prüfer, Kay
Lambert, David
Kelso, Janet
Schöneberg, Torsten
author_facet Le Duc, Diana
Renaud, Gabriel
Krishnan, Arunkumar
Almén, Markus Sällman
Huynen, Leon
Prohaska, Sonja J.
Ongyerth, Matthias
Bitarello, Bárbara D.
Schiöth, Helgi B.
Hofreiter, Michael
Stadler, Peter F.
Prüfer, Kay
Lambert, David
Kelso, Janet
Schöneberg, Torsten
author_sort Le Duc, Diana
collection PubMed
description BACKGROUND: Kiwi, comprising five species from the genus Apteryx, are endangered, ground-dwelling bird species endemic to New Zealand. They are the smallest and only nocturnal representatives of the ratites. The timing of kiwi adaptation to a nocturnal niche and the genomic innovations, which shaped sensory systems and morphology to allow this adaptation, are not yet fully understood. RESULTS: We sequenced and assembled the brown kiwi genome to 150-fold coverage and annotated the genome using kiwi transcript data and non-redundant protein information from multiple bird species. We identified evolutionary sequence changes that underlie adaptation to nocturnality and estimated the onset time of these adaptations. Several opsin genes involved in color vision are inactivated in the kiwi. We date this inactivation to the Oligocene epoch, likely after the arrival of the ancestor of modern kiwi in New Zealand. Genome comparisons between kiwi and representatives of ratites, Galloanserae, and Neoaves, including nocturnal and song birds, show diversification of kiwi’s odorant receptors repertoire, which may reflect an increased reliance on olfaction rather than sight during foraging. Further, there is an enrichment of genes influencing mitochondrial function and energy expenditure among genes that are rapidly evolving specifically on the kiwi branch, which may also be linked to its nocturnal lifestyle. CONCLUSIONS: The genomic changes in kiwi vision and olfaction are consistent with changes that are hypothesized to occur during adaptation to nocturnal lifestyle in mammals. The kiwi genome provides a valuable genomic resource for future genome-wide comparative analyses to other extinct and extant diurnal ratites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0711-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-45119692015-07-24 Kiwi genome provides insights into evolution of a nocturnal lifestyle Le Duc, Diana Renaud, Gabriel Krishnan, Arunkumar Almén, Markus Sällman Huynen, Leon Prohaska, Sonja J. Ongyerth, Matthias Bitarello, Bárbara D. Schiöth, Helgi B. Hofreiter, Michael Stadler, Peter F. Prüfer, Kay Lambert, David Kelso, Janet Schöneberg, Torsten Genome Biol Research BACKGROUND: Kiwi, comprising five species from the genus Apteryx, are endangered, ground-dwelling bird species endemic to New Zealand. They are the smallest and only nocturnal representatives of the ratites. The timing of kiwi adaptation to a nocturnal niche and the genomic innovations, which shaped sensory systems and morphology to allow this adaptation, are not yet fully understood. RESULTS: We sequenced and assembled the brown kiwi genome to 150-fold coverage and annotated the genome using kiwi transcript data and non-redundant protein information from multiple bird species. We identified evolutionary sequence changes that underlie adaptation to nocturnality and estimated the onset time of these adaptations. Several opsin genes involved in color vision are inactivated in the kiwi. We date this inactivation to the Oligocene epoch, likely after the arrival of the ancestor of modern kiwi in New Zealand. Genome comparisons between kiwi and representatives of ratites, Galloanserae, and Neoaves, including nocturnal and song birds, show diversification of kiwi’s odorant receptors repertoire, which may reflect an increased reliance on olfaction rather than sight during foraging. Further, there is an enrichment of genes influencing mitochondrial function and energy expenditure among genes that are rapidly evolving specifically on the kiwi branch, which may also be linked to its nocturnal lifestyle. CONCLUSIONS: The genomic changes in kiwi vision and olfaction are consistent with changes that are hypothesized to occur during adaptation to nocturnal lifestyle in mammals. The kiwi genome provides a valuable genomic resource for future genome-wide comparative analyses to other extinct and extant diurnal ratites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-015-0711-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-07-23 2015 /pmc/articles/PMC4511969/ /pubmed/26201466 http://dx.doi.org/10.1186/s13059-015-0711-4 Text en © Le Duc et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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
Le Duc, Diana
Renaud, Gabriel
Krishnan, Arunkumar
Almén, Markus Sällman
Huynen, Leon
Prohaska, Sonja J.
Ongyerth, Matthias
Bitarello, Bárbara D.
Schiöth, Helgi B.
Hofreiter, Michael
Stadler, Peter F.
Prüfer, Kay
Lambert, David
Kelso, Janet
Schöneberg, Torsten
Kiwi genome provides insights into evolution of a nocturnal lifestyle
title Kiwi genome provides insights into evolution of a nocturnal lifestyle
title_full Kiwi genome provides insights into evolution of a nocturnal lifestyle
title_fullStr Kiwi genome provides insights into evolution of a nocturnal lifestyle
title_full_unstemmed Kiwi genome provides insights into evolution of a nocturnal lifestyle
title_short Kiwi genome provides insights into evolution of a nocturnal lifestyle
title_sort kiwi genome provides insights into evolution of a nocturnal lifestyle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511969/
https://www.ncbi.nlm.nih.gov/pubmed/26201466
http://dx.doi.org/10.1186/s13059-015-0711-4
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