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Article|02 Apr 2023|OPEN
QTL detection and candidate gene analysis of grape white rot resistance by interspecific grape (Vitis vinifera L. × Vitis davidii Foex.) crossing
Peng Li1,2 , Xibei Tan1 , Ruitao Liu1 , Faiz Ur Rahman1 , Jianfu Jiang1 , Lei Sun1 , Xiucai Fan1 , Jihong Liu2 , and Chonghuai Liu1 , , Ying Zhang,1,3 ,
1National Key Laboratory for Germplasm Innovation and Utilization of Horticultural Crops, Zhengzhou Fruit Research Institute, Chinese Academy of Agricultural Sciences, Zhengzhou 450000, China
2Key Laboratory of Horticultural Plant Biology (MOE), College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan 430000, China
3Zhongyuan Research Center, Chinese Academy of Agricultural Sciences
*Corresponding author. E-mail: liujihong@mail.hzau.edu.cn,liuchonghuai@caas.cn,zhangying05@caas.cn

Horticulture Research 10,
Article number: uhad063 (2023)
doi: https://doi.org/10.1093/hr/uhad063
Views: 263

Received: 12 Dec 2022
Revised: 02 Apr 2023
Published online: 02 Apr 2023

Abstract

Grape white rot, a devastating disease of grapevines caused by Coniella diplodiella (Speg.) Sacc., leads to significant yield losses in grape. Breeding grape cultivars resistant to white rot is essential to reduce the regular use of chemical treatments. In recent years, Chinese grape species have gained more attention for grape breeding due to their high tolerance to various biotic and abiotic factors along with changing climatic conditions. In this study, we employed whole-genome resequencing (WGR) to genotype the parents of ‘Manicure Finger’ (Vitis vinifera, female) and ‘0940’ (Vitis davidii, male), along with 101 F1 mapping population individuals, thereby constructing a linkage genetic map. The linkage map contained 9337 single-nucleotide polymorphism (SNP) markers with an average marker distance of 0.3 cM. After 3 years of phenotypic evaluation of the progeny for white rot resistance, we confirmed one stable quantitative trait locus (QTL) for white rot resistance on chromosome 3, explaining up to 17.9% of the phenotypic variation. For this locus, we used RNA-seq to detect candidate gene expression and identified PR1 as a candidate gene involved in white rot resistance. Finally, we demonstrated that recombinant PR1 protein could inhibit the growth of C. diplodiella and that overexpression of PR1 in susceptible V. vinifera increased grape resistance to the pathogen.