Validation and delineation of a locus conferring Fusarium crown rot resistance on 1HL in barley by analysing transcriptomes from multiple pairs of near isogenic lines

被引:14
作者
Gao, Shang [1 ,2 ,3 ]
Zheng, Zhi [1 ]
Powell, Jonathan [1 ]
Habib, Ahsan [1 ,2 ,3 ,4 ]
Stiller, Jiri [1 ]
Zhou, Meixue [2 ,3 ]
Liu, Chunji [1 ]
机构
[1] CSIRO Agr & Food, St Lucia, Qld 4067, Australia
[2] Univ Tasmania, Sch Land & Food, Hobart, Tas, Australia
[3] Univ Tasmania, Tasmanian Inst Agr, Hobart, Tas, Australia
[4] Khulna Univ, Biotechnol & Genet Engn Discipline, Khulna 9208, Bangladesh
关键词
Fusarium crown rot; QTL validation; Near-isogenic line; RNA-seq; Transcriptome; Barley; HEAD BLIGHT RESISTANCE; LOOP NTPASE OSYCHF1; LARGE-EFFECT QTL; BREAD WHEAT; MAJOR QTL; RNA-SEQ; UDP-GLUCOSYLTRANSFERASE; DEFENSE RESPONSES; LONG ARM; PATHOGEN;
D O I
10.1186/s12864-019-6011-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Fusarium crown rot (FCR) is a chronic and severe disease in cereal production in semi-arid regions worldwide. A putative quantitative trait locus conferring FCR resistance, Qcrs.cpi-1H, had previously been mapped on the long arm of chromosome 1H in barley. Results In this study, five pairs of near-isogenic lines (NILs) targeting the 1HL locus were developed. Analysing the NILs found that the resistant allele at Qcrs.cpi-1H significantly reduced FCR severity. Transcriptomic analysis was then conducted against three of the NIL pairs, which placed the Qcrs.cpi-1H locus in an interval spanning about 11 Mbp. A total of 56 expressed genes bearing single nucleotide polymorphisms (SNPs) were detected in this interval. Five of them contain non-synonymous SNPs. These results would facilitate detailed mapping as well as cloning gene(s) underlying the resistance locus. Conclusion NILs developed in this study and the transcriptomic sequences obtained from them did not only allow the validation of the resistance locus Qcrs.cpi-1H and the identification of candidate genes underlying its resistance, they also allowed the delineation of the resistance locus and the development of SNPs markers which formed a solid base for detailed mapping as well as cloning gene(s) underlying the locus.
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页数:11
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