Scientia Agricultura Sinica ›› 2021, Vol. 54 ›› Issue (2): 310-323.doi: 10.3864/j.issn.0578-1752.2021.02.007

• PLANT PROTECTION • Previous Articles     Next Articles

Expression of Stilbene Synthase Genes from Chinese Wild Vitis quinquangularis and Its Effect on Resistance of Grape to Powdery Mildew

DING Xi(),ZHAO KaiXi,WANG YueJin()   

  1. College of Horticulture, Northwest A & F University/State Key Laboratory of Crop Stress Biology in Arid Areas/Key Laboratory of Horticultural Plant Germplasm Resource Utilization in Northwest China, Ministry of Agriculture and Rural Affairs, Yangling 712100, Shaanxi
  • Received:2020-04-20 Accepted:2020-06-05 Online:2021-01-16 Published:2021-02-03
  • Contact: YueJin WANG E-mail:903735326@qq.com;wangyj@nwsuaf.edu.cn

Abstract:

【Objective】Two stilbene synthase (STS) genes from Chinese wild Vitis quinquangularis ‘Danfeng-2’ (VqSTS9 and VqSTS21) were cloned and functionally investigated with the aim to provide a theoretical basis for improving the disease-resistance and quality of V. vinifera.【Method】Homologous cloning was applied to obtain VqSTS9 and VqSTS21 and their overexpression vectors under the control of CaMV35 promoter were constructed, respectively. The calluses were induced from single bud segment of V. vinifera cv. ‘Thompson Seedless’, which were used as the receptor materials. The resistant ‘Thompson Seedless’ plants were obtained via Agrobacterium-mediated genetic transformation. Furthermore, the disease-resistant transgenic plants were determined by different levels of detection. The leaves of wild-type (WT) and transgenic plants were inoculated with Uncinula necator, the pathogenic conditions of leaves infected with U. necator were observed by microscope to compare their resistance. The expressions of STS and other genes in the metabolic pathway of resveratrol synthesis were analyzed by quantitative real-time PCR (qRT-PCR) in WT and transgenic plants under natural conditions and after inoculation with U. necator. The types and contents of stilbenoids in transgenic plants were determined by HPLC.【Result】The cDNA sequences of VqSTS9 (JQ868689) and VqSTS21 (JQ868677) from the Chinese wild V. quinquangular accession ‘Danfeng-2’ were cloned, and both were 1 179 bp in length. Four VqSTS9-overexpressing and three VqSTS21-overexpressing plants were confirmed by PCR and Western blot analysis. These transgenic plants enhanced resistance to powdery mildew and reduced hyphae growth compared with WT plants through observing the growth of U. necator. The qRT-PCR results indicated that VqSTS9 and VqSTS21 transgenic plants increased the expressions of STS, its upstream PAL, the downstream RSGT, and transcription factor genes MYB14, MYB15 under the natural conditions when compared with WT plants. However, the expression of CHS was down-regulated. After inoculation, the expression of STS in transgenic plants was significantly up-regulated compared to WT. HPLC determination demonstrated that the stilbenoids mainly existed as the form of trans-piceid, and its content in transgenic plants was higher than that in WT under natural conditions. After inoculation, the expression of STS was induced, and trans-piceid, trans-resveratrol and viniferin were also produced. Compared with WT plants, the types and contents of stilbenoids in transgenic plants increased.【Conclusion】Overexpression of VqSTS9 and VqSTS21 in ‘Thompson Seedless’ can enhance the expression of STS, increase the types and contents of stilbenoids, and further inhibit the growth of U. necator. Therefore, ‘Danfeng-2’ is an important germplasm resource for disease-resistant breeding and quality improvement of V. vinifera. Stilbene synthase genes VqSTS9 and VqSTS21 can improve resistance to powdery mildew of V. vinifera.

Key words: Chinese wild Vitis quinquangularis, stilbene synthase gene (STS), resveratrol, powdery mildew, genetic transformation, disease-resistance

Table 1

Primers used in the study"

基因
Gene
上游引物
Forward primer
下游引物
Reverse primer
目标大小
Target size (bp)
VqSTS9 (vector construction, PCR detection) F: CGGGATCCATGGCTTCAGTCGAGGAA TTTAGAAACG R: GCGTCGACATTTGTAACCGTAGGAAT GCTATGCAGC 1179
VqSTS21 (vector construction, PCR detection) F: CGGGATCCATGGCTTCAGTCGAGGAA ATTAGAAACG R: GCGTCGACATTTGTAACCATAGGAAT GCTATGCAACAC 1179

Fig. 1

The expression of VqSTS9 (A), VqSTS21 (B) induced by U. necator"

Fig. 2

Cloning, sequence and cluster analyses of VqSTS9, VqSTS21"

Fig. 3

VqSTS9 and VqSTS21 gene cloning and plant expression vector construction"

Fig. 4

The genetic transformation of Thompson Seedless (A) and identification of transgenic plants (B)"

Fig. 5

STS metabolic pathway related gene expression in WT and transgenic lines"

Fig. 6

Analysis of the resistance to powdery mildew of transgenic plants"

Table 2

Amounts of germination, primary hyphae, secondary hyphae and conidiophore of per 100 spores"

株系
Line
1 dpi 2 dpi 3 dpi 7 dpi
萌发数
Germination
初级菌丝数
Primary hyphae
次级菌丝数
Secondary hyphae
萌发数
Germination
初级菌丝数
Primary hyphae
次级菌丝数
Secondary hyphae
萌发数Germination 初级菌丝数
Primary hyphae
次级菌丝数
Secondary hyphae
分生孢子
梗数
Conidiophore
WT 35.67±2.05a 16.67±1.25a 2.33±0.47a 25.67±1.70a 10.33±1.25d 36.67±1.70a 14.67±1.25d 8.67±1.25c 45.00±1.63a 203.33±5.31a
OEVqSTS9-L1 21.33±2.36c 5.67±1.25d 0 14.67±1.25cd 12.67±2.05cd 5.33±1.25b 22.33±2.49bc 15.33±1.25a 13.67±1.25c 61.33±3.86e
OEVqSTS9-L2 16.67±1.70d 8.00±2.45cd 1.33±1.25a 11.33±1.25d 14.67±0.94bc 6.67±1.70b 21.67±1.70c 11.67±1.25b 16.33±0.47bc 77.00±3.56d
OEVqSTS21-L2 26.67±2.05b 10.67±1.70bc 1.33±1.89a 19.00±1.63b 17.33±1.25ab 7.33±1.25b 27.33±1.25a 14.33±1.70ab 16.33±2.49bc 87.33±3.68c
OEVqSTS21-L3 22.33±1.7bc 13.00±0.82b 0.67±0.94a 17.33±1.70bc 19.33±1.25a 8.33±1.25b 25.67±0.47ab 16.00±0.82a 18.00±1.63b 124.67±4.11b

Fig. 7

The relative expression levels of VqSTS9 and VqSTS21 and the contents and types of stilbenes in overexpressed plants induced by U. necator"

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