Genome-wide identification and analysis of anthocyanin synthesis-related R2R3-MYB genes in Fragaria pentaphylla

被引:1
|
作者
Xie, Liangmu [1 ,2 ]
Wang, Yinuo [1 ,2 ]
Tao, Yutian [2 ,3 ]
Chen, Luxi [2 ]
Lin, Hanyang [2 ,4 ]
Qi, Zhechen [1 ]
Li, Junmin [2 ,4 ]
机构
[1] Zhejiang Sci Tech Univ, Coll Life Sci & Med, Zhejiang Prov Key Lab Plant Secondary Metab & Regu, Hangzhou 310018, Peoples R China
[2] Taizhou Univ, Sch Life Sci, Zhejiang Prov Key Lab Plant Evolutionary Ecol & Co, Taizhou 318000, Peoples R China
[3] Taizhou Univ, Sch Elect & Informat Engn, Taizhou 318000, Peoples R China
[4] Taizhou Univ, Sch Adv Study, Taizhou 318000, Peoples R China
来源
BMC GENOMICS | 2024年 / 25卷 / 01期
基金
中国国家自然科学基金;
关键词
Fragaria pentaphylla; Anthocyanin biosynthesis; Subcellular localization; Transcriptome; MYB TRANSCRIPTION FACTORS; PROTEINS; BIOSYNTHESIS; EXPRESSION; TOBACCO; FAMILY; WHITE; WD40; RED;
D O I
10.1186/s12864-024-10882-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background MYB transcription factors regulate anthocyanin biosynthesis across numerous plant species. However, comprehensive genome-wide investigations regarding the R2R3-MYB gene family and its involvement in regulating anthocyanin biosynthesis in the red and white fruit color morphs of Fragaria pentaphylla remain scarce. Results A total of 101 FpR2R3-MYB genes were identified from the F. pentaphylla genome and were divided into 34 subgroups based on phylogenetic analysis. Gene structure (exon/intron) and protein motifs were particularly conserved among the FpR2R3-MYB genes, especially members within the same subgroup. The FpR2R3-MYB genes were distributed over seven F. pentaphylla chromosomes. Analysis of gene duplication events revealed five pairs of tandem duplication genes and 16 pairs of segmental duplication genes, suggesting that segmental duplications are the major pattern for expansion of the FpR2R3-MYB gene family expansion in F. pentaphylla. Cis-regulatory elements of the FpR2R3-MYB promoters were involved in cellular development, phytohormones, environmental stress and photoresponse. Based on the analysis of the FpR2R3-MYB gene family and transcriptome sequencing (RNA-seq) data, FpMYB9 was identified as a key transcription factor involved in the regulation of anthocyanin synthesis in F. pentaphylla fruits. The expression of FpMYB9 increases significantly during the ripening stage of red fruits, as confirmed by reverse transcription quantitative real-time PCR. In addition, subcellular localization experiments further confirmed the nuclear presence of FpMYB9, supporting its role as a transcription factor involved in anthocyanin biosynthesis. Conclusion Our results showed that the FpR2R3-MYB genes are highly conserved and play important roles in the anthocyanin biosynthesis in F. pentaphylla fruits. Our results also provide a compelling basis for further understanding of the regulatory mechanism underlying the role of FpMYB9 in anthocyanin formation in F. pentaphylla fruits.
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页数:16
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