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大豆对2种类型SMV分离物的抗性遗传分析及QTL定位

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[目的]为了挖掘大豆抗重组型大豆花叶病毒(soybean mosaic virus,SMV)的基因资源,进一步为探索抗重组型SMV与抗非重组型SMV遗传和分子机制差异提供支撑。[方法]以冀豆17(抗病)×绥农14(感病)构建的包含272个家系的重组自交系(RIL)群体为材料,在2种不同环境下对非重组型SMV(HB-SC3)和重组型SMV(HB-RS)株系进行抗性遗传定位分析及分子机制探索。[结果]RIL群体在2种环境下接种HB-SC3和HB-RS后抗感家系分离比均符合1∶1抗感分离比(P>0。05),且F1植株对HB-SC3和HB-RS均表现为抗病,表明冀豆17携带对2种类型SMV的抗性均由1对主效显性基因控制。但受HB-SC3和HB-RS侵染后,不同级别的感病家系在不同环境下变化幅度较大,分别为4。3%~22。2%和11。1%~129。63%之间,表明环境对HB-RS侵染植株后的症状影响显著。QTL分析共定位到3个QTL位点,其中qRsmv13为稳定的主效QTL位点,对2种类型SMV均具有显著抗性,LOD值在23。94~40。42之间,可解释遗传变异率在35。80%~50。46%之间,抗性增效基因来源于冀豆17。此外,2个微效QTL位点qRsmv7和qRsmv14的LOD值分别为2。95和2。62,可分别解释2。58%和2。72%的表型变异,抗性增效基因也均来源于冀豆17。结果还显示,感病植株HB-SC3的浓度显著高于HB-RS约20倍,植株接种HB-SC3后可引起3个与坏死相关的PR1基因的上调表达,且3个PR1基因表达量显著高于接种HB-RS的植株,表明2种类型SMV致病分子机制存在显著的差异。[结论]大豆抗重组型SMV主效QTL位点为qRsmv13,微效位点为qRsmv7和qRsmv14,抗重组型SMV与抗非重组型SMV遗传和分子机制存在显著差异。
Genetic Analysis and QTL Mapping of Soybean Resistance to Two Types of SMV Virus
[Objective]This study aims to explore the genetic resources conferring resistance to soybean mosaic virus(SMV)and to provide further support for understanding the differences in genetic and mo-lecular mechanisms between resistance to recombinant and non-recombinant SMV.[Method]A recom-binant inbred line(RIL)population,comprising 272 families derived from the cross between Ji Dou 17(resistant)and Sui Nong 14(susceptible),was utilized to determine the genetic basis and molecular mechanisms under two distinct environmental conditions.[Result]Following inoculation of the RIL population with HB-SC3 and HB-RS,the segregation ratio of resistant to susceptible lines was found to fit a 1∶1 ratio according to the Chi-square test(P>0.05).F1 plants exhibited resis-tance to both HB-SC3 and HB-RS,suggesting that Ji Dou 17 contains a dominant gene confer-ring resistance to both strains.However,the susceptibility grades of families infected with HB-SC3 and HB-RS showed significant shifts,with variations of 4.3%-22.2%and 11.1%-129.63%under different environments,respectively,indicating a substantial environmental impact on the symptoms of plants infected with HB-RS.Additionally,three QTLs were identified through QTL analysis.Notably,qRsmv13 is a stable and dominant QTL that confers resistance to both SMV strains,with LOD values ranging from 23.94 to 40.42 and explaining 35.80%-50.46%of the ge-netic variation.The additive gene effect for resistance to both strains was traced back to Ji Dou 17.Furthermore,the LOD values for the two minor QTLs,qRsmv7 and qRsmv14,were 2.95 and 2.62,respectively,accounting for 2.58%and 2.72%of the phenotypic variation.The addi-tive gene effects for these QTLs also originated from Ji Dou 17.The results further demonstrated that the concentration of HB-SC3 in infected plants was approximately 20 times higher than that of HB-RS,and three PR1 genes associated with necrosis were up-regulated following inocula-tion with HB-SC3.The expression levels of these PR1 genes were significantly higher than those observed with HB-RS,suggesting distinct molecular mechanisms between the two SMV strains.[Conclusion]The primary QTL for soybean resistance to recombinant SMV is qRsmv13,with minor effect loci being qRsmv7 and qRsmv14.There are significant differences in the genetic and molecu-lar mechanisms between resistance to recombinant and non-recombinant SMV strains.

soybeansoybean mosaic virusresistanceQTLnecrosis related gene

高齐齐、刘兵强、赵田湉、陈强、史晓蕾、林静、杨春燕、张孟臣

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河北科技师范学院,河北 秦皇岛 066004

河北省农林科学院粮油作物研究所/国家大豆改良中心石家庄分中心/农业农村部黄淮海大豆生物学与遗传育种重点实验室/河北省作物遗传育种重点实验室,石家庄 050035

大豆 大豆花叶病毒 抗性 QTL 坏死相关基因

2024

四川农业大学学报
四川农业大学

四川农业大学学报

CSTPCD北大核心
影响因子:0.657
ISSN:1000-2650
年,卷(期):2024.42(6)