Fine mapping of a Fusarium crown rot resistant locus on chromosome arm 6HL in barley by exploiting near isogenic lines, transcriptome profiling, and a large near isogenic line-derived population

被引:4
|
作者
Gao, Shang [1 ,2 ,3 ]
Jiang, Yunfeng [1 ,4 ]
Zhou, Hong [1 ,4 ]
Liu, Yaxi [4 ]
Li, Huihui [2 ,3 ]
Liu, Chunji [1 ]
Zheng, Zhi [1 ]
机构
[1] CSIRO Agr & Food, 306 Carmody Rd, St Lucia, QLD 4067, Australia
[2] Chinese Acad Agr Sci, Inst Crop Sci, CIMMYT China Off, 12 Zhongguancun South St, Beijing 100081, Peoples R China
[3] Chinese Acad Agr Sci, Nanfan Res Inst, Sanya 572024, Hainan, Peoples R China
[4] Sichuan Agr Univ, Triticeae Res Inst, Chengdu 611130, Peoples R China
关键词
E3 UBIQUITIN LIGASE; HEAD BLIGHT; MAJOR QTL; BREAD WHEAT; CELL-DEATH; RNA-SEQ; PSEUDOGRAMINEARUM; PATHOGENS; DEFENSE; IDENTIFICATION;
D O I
10.1007/s00122-023-04387-x
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Key messageThis study reported validation and fine mapping of a Fusarium crown rot resistant locus on chromosome arm 6HL in barley using near isogenic lines, transcriptome sequences, and a large near isogenic line-derived population.Fusarium crown rot (FCR), caused by Fusarium pseudograminearum, is a chronic and serious disease affecting cereal production in semi-arid regions globally. The increasing prevalence of this disease in recent years is attributed to the widespread adoption of minimum tillage and stubble retention practices. In the study reported here, we generated eight pairs of near isogenic lines (NILs) targeting a putative QTL (Qcrs.caf-6H) conferring FCR resistance in barley. Assessing the NILs confirmed the large effect of this locus. Aimed to develop markers that can be reliably used in incorporating this resistant allele into breeding programs and identify candidate genes, transcriptomic analyses were conducted against three of the NIL pairs and a large NIL-derived population consisting of 1085 F7 recombinant inbred lines generated. By analyzing the transcriptomic data and the fine mapping population, Qcrs.caf-6H was delineated into an interval of 0.9 cM covering a physical distance of similar to 547 kb. Six markers co-segregating with this locus were developed. Based on differential gene expression and SNP variations between the two isolines among the three NIL pairs, candidate genes underlying the resistance at this locus were detected. These results would improve the efficiency of incorporating the targeted locus into barley breeding programs and facilitate the cloning of causal gene(s) responsible for the resistance.
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页数:12
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