Comprehensive Genomic Identification and Characterization of R2R3-MYB Genes in Colored Rice (Oryza sativa L.): A Phylogenetic and Expression Analysis  

lijuan chen
Author    Correspondence author
Genomics and Applied Biology, 2024, Vol. 15, No.   
Received: 01 Jan., 1970    Accepted: 01 Jan., 1970    Published: 13 Aug., 2024
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Abstract
This study provides a comprehensive identification and characterization of the R2R3-MYB gene family in colored rice (Oryza sativa L.), offering significant insights into their evolutionary relationships, structural features, and expression profiles. Notable findings include the distinctive structural characteristics of R2R3-MYB genes, such as the high prevalence of non-synonymous substitutions in the DNA-binding domains, particularly in the α-helix regions. This suggests adaptive selection and functional diversification. The phylogenetic analysis revealed the existence of distinct clades that correspond to different evolutionary lineages. Of particular interest is a key clade that is closely related to the ancestral species, wild rice (O. rufipogon and O. nivara), which indicates the conservation of evolutionary lineages. The expression patterns of R2R3-MYB genes were found to be specific to different tissues and developmentally regulated, with specialized roles in photosynthesis-related processes and root development. Furthermore, the study underscores the functional roles of R2R3-MYB genes in anthocyanin biosynthesis. Genes such as OsC1 and OsKala3 play pivotal roles in modulating the expression of anthocyanin biosynthetic pathway genes, thereby contributing to the distinctive purple pigmentation and associated health benefits of purple rice. Furthermore, the case study of OsMYB30 and OsMYB60 illustrates their pivotal roles in plant defense mechanisms and leaf morphology, respectively. The insights gained from this study have significant implications for the breeding and genetic engineering of colored rice, emphasizing the potential for improving agronomic traits and enhancing crop performance through targeted manipulation of R2R3-MYB genes.
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