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

• Published in: PloS one 2011-03, Vol.6 (3), p.e16079
• Main Authors: Sun, Xinli, Wang, Guo-Liang
• Format: Article
• Language: English
• Subjects: Amino Acid Motifs; Amino Acid Sequence; Amino acids; Analysis; Annotations; Arabidopsis; Base Sequence; Bioinformatics; Biology; Cladistic analysis; Evolution & development; Evolution, Molecular; Exons; Exons - genetics; Gene Duplication - genetics; Genes; Genes, Plant - genetics; Genetic aspects; Genetic Variation; Genome, Plant - genetics; Genomes; Genomics; Introns; Introns - genetics; Kinases; Molecular Sequence Annotation; Molecular Sequence Data; Multigene Family; Mutation; Nucleotide sequence; Oryza; Oryza - enzymology; Oryza - genetics; Oryza sativa; Phosphotransferases; Phylogenetics; Phylogeny; Plant pathology; Plant Proteins - chemistry; Plant Proteins - genetics; Positive selection; Protein interaction; Protein Kinases - chemistry; Protein Kinases - genetics; Protein Sorting Signals - genetics; Protein Structure, Tertiary; Protein-protein interactions; Proteins; Reproduction (copying); Selection, Genetic; Statistical methods; Xanthomonas campestris
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0016079

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.