Cargando…

Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths

Chemical signals are prevalent in sexual communication systems. Mate recognition has been extensively studied within the Lepidoptera, where the production and recognition of species-specific sex pheromone signals are typically the defining character. While the specific blend of compounds that makes...

Descripción completa

Detalles Bibliográficos
Autores principales: Albre, Jérôme, Liénard, Marjorie A., Sirey, Tamara M., Schmidt, Silvia, Tooman, Leah K., Carraher, Colm, Greenwood, David R., Löfstedt, Christer, Newcomb, Richard D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266893/
https://www.ncbi.nlm.nih.gov/pubmed/22291612
http://dx.doi.org/10.1371/journal.pgen.1002489
_version_ 1782222220181897216
author Albre, Jérôme
Liénard, Marjorie A.
Sirey, Tamara M.
Schmidt, Silvia
Tooman, Leah K.
Carraher, Colm
Greenwood, David R.
Löfstedt, Christer
Newcomb, Richard D.
author_facet Albre, Jérôme
Liénard, Marjorie A.
Sirey, Tamara M.
Schmidt, Silvia
Tooman, Leah K.
Carraher, Colm
Greenwood, David R.
Löfstedt, Christer
Newcomb, Richard D.
author_sort Albre, Jérôme
collection PubMed
description Chemical signals are prevalent in sexual communication systems. Mate recognition has been extensively studied within the Lepidoptera, where the production and recognition of species-specific sex pheromone signals are typically the defining character. While the specific blend of compounds that makes up the sex pheromones of many species has been characterized, the molecular mechanisms underpinning the evolution of pheromone-based mate recognition systems remain largely unknown. We have focused on two sets of sibling species within the leafroller moth genera Ctenopseustis and Planotortrix that have rapidly evolved the use of distinct sex pheromone blends. The compounds within these blends differ almost exclusively in the relative position of double bonds that are introduced by desaturase enzymes. Of the six desaturase orthologs isolated from all four species, functional analyses in yeast and gene expression in pheromone glands implicate three in pheromone biosynthesis, two Δ9-desaturases, and a Δ10-desaturase, while the remaining three desaturases include a Δ6-desaturase, a terminal desaturase, and a non-functional desaturase. Comparative quantitative real-time PCR reveals that the Δ10-desaturase is differentially expressed in the pheromone glands of the two sets of sibling species, consistent with differences in the pheromone blend in both species pairs. In the pheromone glands of species that utilize (Z)-8-tetradecenyl acetate as sex pheromone component (Ctenopseustis obliquana and Planotortrix octo), the expression levels of the Δ10-desaturase are significantly higher than in the pheromone glands of their respective sibling species (C. herana and P. excessana). Our results demonstrate that interspecific sex pheromone differences are associated with differential regulation of the same desaturase gene in two genera of moths. We suggest that differential gene regulation among members of a multigene family may be an important mechanism of molecular innovation in sex pheromone evolution and speciation.
format Online
Article
Text
id pubmed-3266893
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32668932012-01-30 Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths Albre, Jérôme Liénard, Marjorie A. Sirey, Tamara M. Schmidt, Silvia Tooman, Leah K. Carraher, Colm Greenwood, David R. Löfstedt, Christer Newcomb, Richard D. PLoS Genet Research Article Chemical signals are prevalent in sexual communication systems. Mate recognition has been extensively studied within the Lepidoptera, where the production and recognition of species-specific sex pheromone signals are typically the defining character. While the specific blend of compounds that makes up the sex pheromones of many species has been characterized, the molecular mechanisms underpinning the evolution of pheromone-based mate recognition systems remain largely unknown. We have focused on two sets of sibling species within the leafroller moth genera Ctenopseustis and Planotortrix that have rapidly evolved the use of distinct sex pheromone blends. The compounds within these blends differ almost exclusively in the relative position of double bonds that are introduced by desaturase enzymes. Of the six desaturase orthologs isolated from all four species, functional analyses in yeast and gene expression in pheromone glands implicate three in pheromone biosynthesis, two Δ9-desaturases, and a Δ10-desaturase, while the remaining three desaturases include a Δ6-desaturase, a terminal desaturase, and a non-functional desaturase. Comparative quantitative real-time PCR reveals that the Δ10-desaturase is differentially expressed in the pheromone glands of the two sets of sibling species, consistent with differences in the pheromone blend in both species pairs. In the pheromone glands of species that utilize (Z)-8-tetradecenyl acetate as sex pheromone component (Ctenopseustis obliquana and Planotortrix octo), the expression levels of the Δ10-desaturase are significantly higher than in the pheromone glands of their respective sibling species (C. herana and P. excessana). Our results demonstrate that interspecific sex pheromone differences are associated with differential regulation of the same desaturase gene in two genera of moths. We suggest that differential gene regulation among members of a multigene family may be an important mechanism of molecular innovation in sex pheromone evolution and speciation. Public Library of Science 2012-01-26 /pmc/articles/PMC3266893/ /pubmed/22291612 http://dx.doi.org/10.1371/journal.pgen.1002489 Text en Albre et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Albre, Jérôme
Liénard, Marjorie A.
Sirey, Tamara M.
Schmidt, Silvia
Tooman, Leah K.
Carraher, Colm
Greenwood, David R.
Löfstedt, Christer
Newcomb, Richard D.
Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths
title Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths
title_full Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths
title_fullStr Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths
title_full_unstemmed Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths
title_short Sex Pheromone Evolution Is Associated with Differential Regulation of the Same Desaturase Gene in Two Genera of Leafroller Moths
title_sort sex pheromone evolution is associated with differential regulation of the same desaturase gene in two genera of leafroller moths
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266893/
https://www.ncbi.nlm.nih.gov/pubmed/22291612
http://dx.doi.org/10.1371/journal.pgen.1002489
work_keys_str_mv AT albrejerome sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT lienardmarjoriea sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT sireytamaram sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT schmidtsilvia sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT toomanleahk sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT carrahercolm sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT greenwooddavidr sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT lofstedtchrister sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths
AT newcombrichardd sexpheromoneevolutionisassociatedwithdifferentialregulationofthesamedesaturasegeneintwogeneraofleafrollermoths