Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species

Nucleotide-binding leucine-rich repeat (NLR) genes play a key role in plant immune responses and have co-evolved with pathogens since the origin of green plants. Comparative genomic studies on the evolution of NLR genes have been carried out in several angiosperm lineages. However, most of these lin...

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Main Authors: Xiao-Tong Li, Guang-Can Zhou, Xing-Yu Feng, Zhen Zeng, Yang Liu, Zhu-Qing Shao
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Horticulturae
Subjects:
Online Access:https://www.mdpi.com/2311-7524/7/12/539
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author Xiao-Tong Li
Guang-Can Zhou
Xing-Yu Feng
Zhen Zeng
Yang Liu
Zhu-Qing Shao
author_facet Xiao-Tong Li
Guang-Can Zhou
Xing-Yu Feng
Zhen Zeng
Yang Liu
Zhu-Qing Shao
author_sort Xiao-Tong Li
collection DOAJ
description Nucleotide-binding leucine-rich repeat (NLR) genes play a key role in plant immune responses and have co-evolved with pathogens since the origin of green plants. Comparative genomic studies on the evolution of NLR genes have been carried out in several angiosperm lineages. However, most of these lineages come from the dicot clade. In this study, comparative analysis was performed on NLR genes from five Arecaceae species to trace the dynamic evolutionary pattern of the gene family during species speciation in this monocot lineage. The results showed that NLR genes from the genomes of <i>Elaeis guineensis</i> (262), <i>Phoenix dactylifera</i> (85), <i>Daemonorops jenkinsiana</i> (536), <i>Cocos nucifera</i> (135) and <i>Calamus simplicifolius</i> (399) are highly variable. Frequent domain loss and alien domain integration have occurred to shape the NLR protein structures. Phylogenetic analysis revealed that NLR genes from the five genomes were derived from dozens of ancestral genes. <i>D. jenkinsiana</i> and <i>E. guineensis</i> genomes have experienced “consistent expansion” of the ancestral NLR lineages, whereas a pattern of “first expansion and then contraction” of NLR genes was observed for <i>P. dactylifera</i>, <i>C. nucifera</i> and <i>C. simplicifolius</i>. The results suggest that rapid and dynamic gene content and structure variation have shaped the NLR profiles of Arecaceae species.
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spelling doaj.art-fb21350807214d9b9069206d8f029b0d2023-11-23T08:37:55ZengMDPI AGHorticulturae2311-75242021-12-0171253910.3390/horticulturae7120539Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae SpeciesXiao-Tong Li0Guang-Can Zhou1Xing-Yu Feng2Zhen Zeng3Yang Liu4Zhu-Qing Shao5School of Life Sciences, Nanjing University, Nanjing 210023, ChinaCollege of Agricultural and Biological Engineering (College of Tree Peony), Heze University, Heze 274015, ChinaSchool of Life Sciences, Nanjing University, Nanjing 210023, ChinaSchool of Life Sciences, Nanjing University, Nanjing 210023, ChinaSchool of Life Sciences, Nanjing University, Nanjing 210023, ChinaSchool of Life Sciences, Nanjing University, Nanjing 210023, ChinaNucleotide-binding leucine-rich repeat (NLR) genes play a key role in plant immune responses and have co-evolved with pathogens since the origin of green plants. Comparative genomic studies on the evolution of NLR genes have been carried out in several angiosperm lineages. However, most of these lineages come from the dicot clade. In this study, comparative analysis was performed on NLR genes from five Arecaceae species to trace the dynamic evolutionary pattern of the gene family during species speciation in this monocot lineage. The results showed that NLR genes from the genomes of <i>Elaeis guineensis</i> (262), <i>Phoenix dactylifera</i> (85), <i>Daemonorops jenkinsiana</i> (536), <i>Cocos nucifera</i> (135) and <i>Calamus simplicifolius</i> (399) are highly variable. Frequent domain loss and alien domain integration have occurred to shape the NLR protein structures. Phylogenetic analysis revealed that NLR genes from the five genomes were derived from dozens of ancestral genes. <i>D. jenkinsiana</i> and <i>E. guineensis</i> genomes have experienced “consistent expansion” of the ancestral NLR lineages, whereas a pattern of “first expansion and then contraction” of NLR genes was observed for <i>P. dactylifera</i>, <i>C. nucifera</i> and <i>C. simplicifolius</i>. The results suggest that rapid and dynamic gene content and structure variation have shaped the NLR profiles of Arecaceae species.https://www.mdpi.com/2311-7524/7/12/539ArecaceaeNLR geneplant disease resistancephylogenyevolutionary pattern
spellingShingle Xiao-Tong Li
Guang-Can Zhou
Xing-Yu Feng
Zhen Zeng
Yang Liu
Zhu-Qing Shao
Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species
Horticulturae
Arecaceae
NLR gene
plant disease resistance
phylogeny
evolutionary pattern
title Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species
title_full Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species
title_fullStr Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species
title_full_unstemmed Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species
title_short Frequent Gene Duplication/Loss Shapes Distinct Evolutionary Patterns of NLR Genes in Arecaceae Species
title_sort frequent gene duplication loss shapes distinct evolutionary patterns of nlr genes in arecaceae species
topic Arecaceae
NLR gene
plant disease resistance
phylogeny
evolutionary pattern
url https://www.mdpi.com/2311-7524/7/12/539
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