Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.

LRR-kinases constitute the largest subfamily of receptor-like kinases in plants and regulate a wide variety of processes related to development and defense. Through a reiterative process of sequence analysis and re-annotation, we identified 309 LRR-kinase genes in the rice genome (Nipponbare). Among...

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Main Authors: Xinli Sun, Guo-Liang Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3050792?pdf=render
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spelling doaj-c71e906ca4d54cef8d3d82f680fe82da2020-11-25T01:00:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0163e1607910.1371/journal.pone.0016079Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.Xinli SunGuo-Liang WangLRR-kinases constitute the largest subfamily of receptor-like kinases in plants and regulate a wide variety of processes related to development and defense. Through a reiterative process of sequence analysis and re-annotation, we identified 309 LRR-kinase genes in the rice genome (Nipponbare). Among them, 127 genes in the Rice Annotation Project Database and 85 in Refseq of NCBI were amended (in addition, 62 LRR-kinase genes were not annotated in Refseq). The complete set of LRR-kinases was characterized. These LRR-kinases were classified into five groups according to phylogenetic analysis, and the genes in groups 1, 2, 3 and 4 usually have fewer introns than those in group 5. The introns in the LRR domain, which are highly conserved in regards to their positions and configurations, split the first Leu or other amino residues at this position of the 'xxLxLxx' motif with phase 2 and usually separate one or more LRR repeats exactly. Tandemly repeated LRR motifs have evolved from exon duplication, mutation and exon shuffling. The extensive distribution and diversity of the LRR-kinase genes have been mainly generated by tandem duplication and mutation after whole genome duplication. Positive selection has made a limited contribution to the sequence diversity after duplication, but positively selected sites located in the LRR domain are thought to involve in the protein-protein interaction.http://europepmc.org/articles/PMC3050792?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Xinli Sun
Guo-Liang Wang
spellingShingle Xinli Sun
Guo-Liang Wang
Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.
PLoS ONE
author_facet Xinli Sun
Guo-Liang Wang
author_sort Xinli Sun
title Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.
title_short Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.
title_full Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.
title_fullStr Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.
title_full_unstemmed Genome-wide identification, characterization and phylogenetic analysis of the rice LRR-kinases.
title_sort genome-wide identification, characterization and phylogenetic analysis of the rice lrr-kinases.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description LRR-kinases constitute the largest subfamily of receptor-like kinases in plants and regulate a wide variety of processes related to development and defense. Through a reiterative process of sequence analysis and re-annotation, we identified 309 LRR-kinase genes in the rice genome (Nipponbare). Among them, 127 genes in the Rice Annotation Project Database and 85 in Refseq of NCBI were amended (in addition, 62 LRR-kinase genes were not annotated in Refseq). The complete set of LRR-kinases was characterized. These LRR-kinases were classified into five groups according to phylogenetic analysis, and the genes in groups 1, 2, 3 and 4 usually have fewer introns than those in group 5. The introns in the LRR domain, which are highly conserved in regards to their positions and configurations, split the first Leu or other amino residues at this position of the 'xxLxLxx' motif with phase 2 and usually separate one or more LRR repeats exactly. Tandemly repeated LRR motifs have evolved from exon duplication, mutation and exon shuffling. The extensive distribution and diversity of the LRR-kinase genes have been mainly generated by tandem duplication and mutation after whole genome duplication. Positive selection has made a limited contribution to the sequence diversity after duplication, but positively selected sites located in the LRR domain are thought to involve in the protein-protein interaction.
url http://europepmc.org/articles/PMC3050792?pdf=render
work_keys_str_mv AT xinlisun genomewideidentificationcharacterizationandphylogeneticanalysisofthericelrrkinases
AT guoliangwang genomewideidentificationcharacterizationandphylogeneticanalysisofthericelrrkinases
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