Genomic footprints of repeated evolution of CAM photosynthesis in a Neotropical species radiation.
Détails
ID Serval
serval:BIB_AF228E1EBF7B
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Genomic footprints of repeated evolution of CAM photosynthesis in a Neotropical species radiation.
Périodique
Plant, cell & environment
ISSN
1365-3040 (Electronic)
ISSN-L
0140-7791
Statut éditorial
Publié
Date de publication
12/2020
Peer-reviewed
Oui
Volume
43
Numéro
12
Pages
2987-3001
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Résumé
The adaptive radiation of Bromeliaceae (pineapple family) is one of the most diverse among Neotropical flowering plants. Diversification in this group was facilitated by shifts in several adaptive traits or "key innovations" including the transition from C <sub>3</sub> to CAM photosynthesis associated with xeric (heat/drought) adaptation. We used phylogenomic approaches, complemented by differential gene expression (RNA-seq) and targeted metabolite profiling, to address the mechanisms of C <sub>3</sub> /CAM evolution in the extremely species-rich bromeliad genus, Tillandsia, and related taxa. Evolutionary analyses of whole-genome sequencing and RNA-seq data suggest that evolution of CAM is associated with coincident changes to different pathways mediating xeric adaptation in this group. At the molecular level, C <sub>3</sub> /CAM shifts were accompanied by gene expansion of XAP5 CIRCADIAN TIMEKEEPER homologs, a regulator involved in sugar- and light-dependent regulation of growth and development. Our analyses also support the re-programming of abscisic acid-related gene expression via differential expression of ABF2/ABF3 transcription factor homologs, and adaptive sequence evolution of an ENO2/LOS2 enolase homolog, effectively tying carbohydrate flux to abscisic acid-mediated abiotic stress response. By pinpointing different regulators of overlapping molecular responses, our results suggest plausible mechanistic explanations for the repeated evolution of correlated adaptive traits seen in a textbook example of an adaptive radiation.
Mots-clé
Biological Evolution, Bromeliaceae/genetics, Bromeliaceae/metabolism, Bromeliaceae/physiology, Crassulacean Acid Metabolism/genetics, Genes, Plant/genetics, Genetic Speciation, Phylogeny, Sequence Analysis, RNA, Whole Exome Sequencing, Whole Genome Sequencing, Bromeliaceae, adaptive radiation, circadian period length, copy number variation, drought, genome, transcriptome
Pubmed
Web of science
Création de la notice
24/07/2020 13:20
Dernière modification de la notice
16/06/2021 5:36