Genome-Wide Identification, Evolution and Functional Divergence of MYB Transcription Factors in Chinese White Pear (Pyrus bretschneideri)

被引:94
|
作者
Li, Xiaolong [1 ]
Xue, Cheng [1 ]
Li, Jiaming [1 ]
Qiao, Xin [1 ]
Li, Leiting [1 ]
Yu, Li'ang [1 ]
Huang, Yuhua [1 ]
Wu, Jun [1 ]
机构
[1] Nanjing Agr Univ, Ctr Pear Engn Technol Res, State Key Lab Crop Genet & Germplasm Enhancement, Nanjing 210095, Jiangsu, Peoples R China
基金
美国国家科学基金会;
关键词
Function; Lignin synthesis; MYB gene family; Pear; DNA-BINDING DOMAIN; LIGNIN BIOSYNTHETIC-PATHWAY; MULTIPLE SEQUENCE ALIGNMENT; CELL-WALL BIOSYNTHESIS; R2R3-MYB GENE FAMILY; ANTHOCYANIN BIOSYNTHESIS; ACID BIOSYNTHESIS; DIRECT TARGET; GLUCOSINOLATE BIOSYNTHESIS; DIFFERENTIAL REGULATION;
D O I
10.1093/pcp/pcw029
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The MYB superfamily is large and functionally diverse in plants. To date, MYB family genes have not yet been identified in Chinese white pear (Pyrus bretschneideri), and their functions remain unclear. In this study, we identified 231 genes as candidate MYB genes and divided them into four subfamilies. The R2R3-MYB (PbrMYB) family shared an R2R3 domain with 104 amino acid residues, including five conserved tryptophan residues. The PbrMYB family was divided into 37 functional subgroups including 33 subgroups which contained both MYB genesof Rosaceae plants and AtMYB genes, and four subgroups which included only Rosaceae MYB genes or AtMYB genes. PbrMYB genes with similar functions clustered into the same subgroup, indicating functional conservation. We also found that whole-genome duplication (WGD) and dispersed duplications played critical roles in the expansion of the MYB family. The 87 PbrMYB duplicated gene pairs dated back to the two WGD events. Purifying selection was the primary force driving PbrMYB gene evolution. The 15 gene pairs presented 1-7 codon sites under positive selection. A total of 147 expressed genes were identified from RNA-sequencing data of fruit, and six PbrMYB members in subgroup C1 were identified as important candidate genes in the regulation of lignin synthesis by quantitative real-time PCR analysis. Further correlation analysis revealed that six PbrMYBs were significantly correlated with five structural gene families (F5H, HCT, CCR, POD and C3'H) in the lignin pathway. The phylogenetic, evolution and expression analyses of the MYB gene family in Chinese white pear establish a solid foundation for future comprehensive functional analysis of PbrMYB genes.
引用
收藏
页码:824 / 847
页数:24
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