Cargando…
Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus)
Carotenoid pigments produce most red, orange and yellow colours in vertebrates. This coloration can serve as an honest signal of quality that mediates social and mating interactions, but our understanding of the underlying mechanisms that control carotenoid signal production, including how different...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542802/ https://www.ncbi.nlm.nih.gov/pubmed/32933448 http://dx.doi.org/10.1098/rspb.2020.1687 |
_version_ | 1783591613086302208 |
---|---|
author | Khalil, Sarah Welklin, Joseph F. McGraw, Kevin J. Boersma, Jordan Schwabl, Hubert Webster, Michael S. Karubian, Jordan |
author_facet | Khalil, Sarah Welklin, Joseph F. McGraw, Kevin J. Boersma, Jordan Schwabl, Hubert Webster, Michael S. Karubian, Jordan |
author_sort | Khalil, Sarah |
collection | PubMed |
description | Carotenoid pigments produce most red, orange and yellow colours in vertebrates. This coloration can serve as an honest signal of quality that mediates social and mating interactions, but our understanding of the underlying mechanisms that control carotenoid signal production, including how different physiological pathways interact to shape and maintain these signals, remains incomplete. We investigated the role of testosterone in mediating gene expression associated with a red plumage sexual signal in red-backed fairywrens (Malurus melanocephalus). In this species, males within a single population can flexibly produce either red/black nuptial plumage or female-like brown plumage. Combining correlational analyses with a field-based testosterone implant experiment and quantitative polymerase chain reaction, we show that testosterone mediates expression of carotenoid-based plumage in part by regulating expression of CYP2J19, a ketolase gene associated with ketocarotenoid metabolism and pigmentation in birds. This is, to our knowledge, the first time that hormonal regulation of a specific genetic locus has been linked to carotenoid production in a natural context, revealing how endocrine mechanisms produce sexual signals that shape reproductive success. |
format | Online Article Text |
id | pubmed-7542802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-75428022020-10-13 Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) Khalil, Sarah Welklin, Joseph F. McGraw, Kevin J. Boersma, Jordan Schwabl, Hubert Webster, Michael S. Karubian, Jordan Proc Biol Sci Evolution Carotenoid pigments produce most red, orange and yellow colours in vertebrates. This coloration can serve as an honest signal of quality that mediates social and mating interactions, but our understanding of the underlying mechanisms that control carotenoid signal production, including how different physiological pathways interact to shape and maintain these signals, remains incomplete. We investigated the role of testosterone in mediating gene expression associated with a red plumage sexual signal in red-backed fairywrens (Malurus melanocephalus). In this species, males within a single population can flexibly produce either red/black nuptial plumage or female-like brown plumage. Combining correlational analyses with a field-based testosterone implant experiment and quantitative polymerase chain reaction, we show that testosterone mediates expression of carotenoid-based plumage in part by regulating expression of CYP2J19, a ketolase gene associated with ketocarotenoid metabolism and pigmentation in birds. This is, to our knowledge, the first time that hormonal regulation of a specific genetic locus has been linked to carotenoid production in a natural context, revealing how endocrine mechanisms produce sexual signals that shape reproductive success. The Royal Society 2020-09-30 2020-09-16 /pmc/articles/PMC7542802/ /pubmed/32933448 http://dx.doi.org/10.1098/rspb.2020.1687 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Evolution Khalil, Sarah Welklin, Joseph F. McGraw, Kevin J. Boersma, Jordan Schwabl, Hubert Webster, Michael S. Karubian, Jordan Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) |
title | Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) |
title_full | Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) |
title_fullStr | Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) |
title_full_unstemmed | Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) |
title_short | Testosterone regulates CYP2J19-linked carotenoid signal expression in male red-backed fairywrens (Malurus melanocephalus) |
title_sort | testosterone regulates cyp2j19-linked carotenoid signal expression in male red-backed fairywrens (malurus melanocephalus) |
topic | Evolution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542802/ https://www.ncbi.nlm.nih.gov/pubmed/32933448 http://dx.doi.org/10.1098/rspb.2020.1687 |
work_keys_str_mv | AT khalilsarah testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus AT welklinjosephf testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus AT mcgrawkevinj testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus AT boersmajordan testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus AT schwablhubert testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus AT webstermichaels testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus AT karubianjordan testosteroneregulatescyp2j19linkedcarotenoidsignalexpressioninmaleredbackedfairywrensmalurusmelanocephalus |