Identification of Clubroot (Plasmodiophora brassicae) Resistance Loci in Chinese Cabbage (Brassica rapa ssp. pekinensis) with Recessive Character

被引:3
作者
Zhang, Hui [1 ]
Liu, Xitong [1 ]
Zhou, Jinyan [1 ]
Strelkov, Stephen E. [2 ]
Fredua-Agyeman, Rudolph [2 ]
Zhang, Shifan [1 ]
Li, Fei [1 ]
Li, Guoliang [1 ]
Wu, Jian [1 ]
Sun, Rifei [1 ]
Hwang, Sheau-Fang [2 ]
Zhang, Shujiang [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Vegetables & Flowers, State Key Lab Vegetable Biobreeding, Beijing 100081, Peoples R China
[2] Univ Alberta, Dept Agr Food & Nutr Sci, Edmonton, AB T6G 2P5, Canada
关键词
Brassica rapa; Plasmodiophora brassicae; resistance gene; QTL; BSA-seq; GENE CONFERRING RESISTANCE; SPECIAL-ISSUE CLUBROOT; DISEASE; CROPS; RICE; RECOGNITION; SUPERFAMILY; ROTATION; MARKERS; TOBACCO;
D O I
10.3390/genes15030274
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The soil-borne pathogen Plasmodiophora brassicae is the causal agent of clubroot, a major disease in Chinese cabbage (Brassica rapa ssp. pekinensis). The host's resistance genes often confer immunity to only specific pathotypes and may be rapidly overcome. Identification of novel clubroot resistance (CR) from germplasm sources is necessary. In this study, Bap246 was tested by being crossed with different highly susceptible B. rapa materials and showed recessive resistance to clubroot. An F-2 population derived from Bap246 x Bac1344 was used to locate the resistance Quantitative Trait Loci (QTL) by Bulk Segregant Analysis Sequencing (BSA-Seq) and QTL mapping methods. Two QTL on chromosomes A01 (4.67-6.06 Mb) and A08 (10.42-11.43 Mb) were found and named Cr4Ba1.1 and Cr4Ba8.1, respectively. Fifteen and eleven SNP/InDel markers were used to narrow the target regions in the larger F-2 population to 4.67-5.17 Mb (A01) and 10.70-10.84 Mb (A08), with 85 and 19 candidate genes, respectively. The phenotypic variation explained (PVE) of the two QTL were 30.97% and 8.65%, respectively. Combined with gene annotation, mutation site analysis, and real-time quantitative polymerase chain reaction (qRT-PCR) analysis, one candidate gene in A08 was identified, namely Bra020861. And an insertion and deletion (InDel) marker (co-segregated) named Crr1-196 was developed based on the gene sequence. Bra013275, Bra013299, Bra013336, Bra013339, Bra013341, and Bra013357 in A01 were the candidate genes that may confer clubroot resistance in Chinese cabbage. The resistance resource and the developed marker will be helpful in Brassica breeding programs.
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页数:17
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