Quantitative Trait Loci Mapping and Development of KASP Marker Smut Screening Assay Using High-Density Genetic Map and Bulked Segregant RNA Sequencing in Sugarcane (Saccharum spp.)
文献类型: 外文期刊
作者: Gao, Yijing 1 ; Zhou, Shan 1 ; Huang, Yuxin 1 ; Zhang, Baoqing 1 ; Xu, Yuhui 2 ; Zhang, Gemin 1 ; Lakshmanan, Prakash 1 ; Yang, Rongzhong 1 ; Zhou, Hui 1 ; Huang, Dongliang 1 ; Liu, Junxian 1 ; Tan, Hongwei 5 ; He, Weizhong 1 ; Yang, Cuifang 1 ; Duan, Weixing 1 ;
作者机构: 1.Chinese Acad Agr Sci, Key Lab Sugarcane Biotechnol & Genet Improvement, Guangxi Key Lab Sugarcane Genet Improvement, Sugarcane Res Ctr,Sugarcane Res Inst,Guangxi Acad, Nanning, Peoples R China
2.Adsen Biotechnol Co Ltd, Urumqi, Peoples R China
3.Southwest Univ, Interdisciplinary Res Ctr Agr Green Dev Yangtze R, Coll Resources & Environm, Chongqing, Peoples R China
4.Univ Queensland, Queensland Alliance Agr & Food Innovat, St Lucia, Qld, Australia
5.Guangxi Acad Agr Sci, Nanning, Peoples R China
关键词: sugarcane; smut; quantitative trait loci (QTL) mapping; bulked segregant RNA sequencing (BSR-seq); kompetitive allele-specific PCR (KASP) markers
期刊名称:FRONTIERS IN PLANT SCIENCE ( 影响因子:6.627; 五年影响因子:7.255 )
ISSN: 1664-462X
年卷期: 2022 年 12 卷
页码:
收录情况: SCI
摘要: Sugarcane is one of the most important industrial crops globally. It is the second largest source of bioethanol, and a major crop for biomass-derived electricity and sugar worldwide. Smut, caused by Sporisorium scitamineum, is a major sugarcane disease in many countries, and is managed by smut-resistant varieties. In China, smut remains the single largest constraint for sugarcane production, and consequently it impacts the value of sugarcane as an energy feedstock. Quantitative trait loci (QTLs) associated with smut resistance and linked diagnostic markers are valuable tools for smut resistance breeding. Here, we developed an F-1 population (192 progeny) by crossing two sugarcane varieties with contrasting smut resistance and used for genome-wide single nucleotide polymorphism (SNP) discovery and mapping, using a high-throughput genotyping method called "specific locus amplified fragment sequencing (SLAF-seq) and bulked-segregant RNA sequencing (BSR-seq). SLAF-seq generated 148,500 polymorphic SNP markers. Using SNP and previously identified SSR markers, an integrated genetic map with an average 1.96 cM marker interval was produced. With this genetic map and smut resistance scores of the F-1 individuals from four crop years, 21 major QTLs were mapped, with a phenotypic variance explanation (PVE) > 8.0%. Among them, 10 QTLs were stable (repeatable) with PVEs ranging from 8.0 to 81.7%. Further, four QTLs were detected based on BSR-seq analysis. aligning major QTLs with the genome of a sugarcane progenitor Saccharum spontaneum, six markers were found co-localized. Markers located in QTLs and functional annotation of BSR-seq-derived unigenes helped identify four disease resistance candidate genes located in major QTLs. 77 SNPs from major QTLs were then converted to Kompetitive Allele-Specific PCR (KASP) markers, of which five were highly significantly linked to smut resistance. The co-localized QTLs, candidate resistance genes, and KASP markers identified in this study provide practically useful tools for marker-assisted sugarcane smut resistance breeding.
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