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Chinese Agricultural Science Bulletin ›› 2024, Vol. 40 ›› Issue (24): 116-121.doi: 10.11924/j.issn.1000-6850.casb2023-0749

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HtMYB2 Gene of Helianthus tuberosus L.: VIGS System Construction and Functional Validation

WANG Ying1,2(), LI Juan1,2, SUN Xuemei1,2()   

  1. 1 Academy of Agriculture & Forestry, Qinghai University, Xining 81000
    2 Laboratory for Research and Utilization of Germplasm Resources in Qinghai-Tibet Plateau, Xining 81000
  • Received:2023-10-04 Revised:2024-01-15 Online:2024-08-20 Published:2024-08-20

Abstract:

Color is an important agronomic trait that affects the value of crops. The purple-skinned Jerusalem artichoke has superior appearance, nutritional value, and commercial value compared to the white-skinned variety. To explore the mechanism of color formation in Jerusalem artichoke tubers, we utilized transcriptome sequencing technology to study both purple and white varieties. We identified the transcription factor HtMYB2, which is associated with anthocyanin synthesis and metabolism. In this study, the HtMYB2 gene in a purple Jerusalem artichoke variety was silenced using virus-induced gene silencing (VIGS) technology to verify its function. Results showed that the tuber epidermis color lightened after infection, anthocyanin content decreased to 15.34 mg/g, HtMYB2 gene expression was 2.06, and silencing efficiency reached 73.96% compared to the control group. It was speculated that silencing the HtMYB2 gene blocked the expression of anthocyanin-related genes in Jerusalem artichoke tubers, leading to reduced anthocyanin synthesis. The HtMYB2 gene positively regulated the anthocyanin synthesis pathway. This study provides a theoretical basis for understanding anthocyanin biosynthesis in the epidermis of Jerusalem artichoke tubers and highlights the importance of HtMYB2 in regulating tuber color and the anthocyanin biosynthesis pathway.

Key words: Helianthus tuberosus L., HtMYB2, anthocyanin, virus-induced gene silencing (VIGS), tuber epidermis color, reverse transcription polymerase chain reaction (rt-pcr), gene expression, biosynthetic pathway