Cargando…

Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana

Herbivore-induced defenses are widespread, rapidly evolving and relevant for plant fitness. Such induced defenses are often mediated by early defense signaling (EDS) rapidly activated by the perception of herbivore associated elicitors (HAE) that includes transient accumulations of jasmonic acid (JA...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Wenwu, Brockmöller, Thomas, Ling, Zhihao, Omdahl, Ashton, Baldwin, Ian T, Xu, Shuqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115867/
https://www.ncbi.nlm.nih.gov/pubmed/27813478
http://dx.doi.org/10.7554/eLife.19531
_version_ 1782468587670208512
author Zhou, Wenwu
Brockmöller, Thomas
Ling, Zhihao
Omdahl, Ashton
Baldwin, Ian T
Xu, Shuqing
author_facet Zhou, Wenwu
Brockmöller, Thomas
Ling, Zhihao
Omdahl, Ashton
Baldwin, Ian T
Xu, Shuqing
author_sort Zhou, Wenwu
collection PubMed
description Herbivore-induced defenses are widespread, rapidly evolving and relevant for plant fitness. Such induced defenses are often mediated by early defense signaling (EDS) rapidly activated by the perception of herbivore associated elicitors (HAE) that includes transient accumulations of jasmonic acid (JA). Analyzing 60 HAE-induced leaf transcriptomes from closely-related Nicotiana species revealed a key gene co-expression network (M4 module) which is co-activated with the HAE-induced JA accumulations but is elicited independently of JA, as revealed in plants silenced in JA signaling. Functional annotations of the M4 module were consistent with roles in EDS and a newly identified hub gene of the M4 module (NaLRRK1) mediates a negative feedback loop with JA signaling. Phylogenomic analysis revealed preferential gene retention after genome-wide duplications shaped the evolution of HAE-induced EDS in Nicotiana. These results highlight the importance of genome-wide duplications in the evolution of adaptive traits in plants. DOI: http://dx.doi.org/10.7554/eLife.19531.001
format Online
Article
Text
id pubmed-5115867
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-51158672016-11-28 Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana Zhou, Wenwu Brockmöller, Thomas Ling, Zhihao Omdahl, Ashton Baldwin, Ian T Xu, Shuqing eLife Genomics and Evolutionary Biology Herbivore-induced defenses are widespread, rapidly evolving and relevant for plant fitness. Such induced defenses are often mediated by early defense signaling (EDS) rapidly activated by the perception of herbivore associated elicitors (HAE) that includes transient accumulations of jasmonic acid (JA). Analyzing 60 HAE-induced leaf transcriptomes from closely-related Nicotiana species revealed a key gene co-expression network (M4 module) which is co-activated with the HAE-induced JA accumulations but is elicited independently of JA, as revealed in plants silenced in JA signaling. Functional annotations of the M4 module were consistent with roles in EDS and a newly identified hub gene of the M4 module (NaLRRK1) mediates a negative feedback loop with JA signaling. Phylogenomic analysis revealed preferential gene retention after genome-wide duplications shaped the evolution of HAE-induced EDS in Nicotiana. These results highlight the importance of genome-wide duplications in the evolution of adaptive traits in plants. DOI: http://dx.doi.org/10.7554/eLife.19531.001 eLife Sciences Publications, Ltd 2016-11-04 /pmc/articles/PMC5115867/ /pubmed/27813478 http://dx.doi.org/10.7554/eLife.19531 Text en © 2016, Zhou et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genomics and Evolutionary Biology
Zhou, Wenwu
Brockmöller, Thomas
Ling, Zhihao
Omdahl, Ashton
Baldwin, Ian T
Xu, Shuqing
Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana
title Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana
title_full Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana
title_fullStr Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana
title_full_unstemmed Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana
title_short Evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in Nicotiana
title_sort evolution of herbivore-induced early defense signaling was shaped by genome-wide duplications in nicotiana
topic Genomics and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115867/
https://www.ncbi.nlm.nih.gov/pubmed/27813478
http://dx.doi.org/10.7554/eLife.19531
work_keys_str_mv AT zhouwenwu evolutionofherbivoreinducedearlydefensesignalingwasshapedbygenomewideduplicationsinnicotiana
AT brockmollerthomas evolutionofherbivoreinducedearlydefensesignalingwasshapedbygenomewideduplicationsinnicotiana
AT lingzhihao evolutionofherbivoreinducedearlydefensesignalingwasshapedbygenomewideduplicationsinnicotiana
AT omdahlashton evolutionofherbivoreinducedearlydefensesignalingwasshapedbygenomewideduplicationsinnicotiana
AT baldwiniant evolutionofherbivoreinducedearlydefensesignalingwasshapedbygenomewideduplicationsinnicotiana
AT xushuqing evolutionofherbivoreinducedearlydefensesignalingwasshapedbygenomewideduplicationsinnicotiana