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A Single-Tube, Functional Marker-Based Multiplex PCR Assay for Simultaneous Detection of Major Bacterial Blight Resistance Genes Xa21, xa13 and xa5 in Rice
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作者 S.K. Hajira R.M. Sundaram +14 位作者 G.S.Laha A.Yugander S.M.Balachandran B.C.Viraktamath K.Sujatha C.H.Balachiranjeevi K.Pranath M.Amla S.Bhaskar V.Abhilash H.K.Mahadevaswamy M.Kousik T.DilipKumar G.Harika G.Rekha 《Rice science》 SCIE CSCD 2016年第3期144-151,共8页
In marker-assisted breeding for bacterial blight(BB) resistance in rice, three major resistance genes, viz., Xa21, xa13 and xa5, are routinely deployed either singly or in combinations. As efficient and functional mar... In marker-assisted breeding for bacterial blight(BB) resistance in rice, three major resistance genes, viz., Xa21, xa13 and xa5, are routinely deployed either singly or in combinations. As efficient and functional markers are yet to be developed for xa13 and xa5, we have developed simple PCR-based functional markers for both the genes. For xa13, we designed a functional PCR-based marker, xa13-prom targeting the In Del polymorphism in the promoter of candidate gene Os8N3 located on chromosome 8 of rice. With respect to xa5, a multiplex-PCR based functional marker system, named xa5 FM, consisting of two sets of primer pairs targeting the 2-bp functional nucleotide polymorphism in the exon II of the gene TFIIA5(candidate for xa5), has been developed. Both xa13-prom and xa5 FM can differentiate the resistant and susceptible alleles for xa13 and xa5, respectively, in a co-dominant fashion. Using these two functional markers along with the already reported functional PCR-based marker for Xa21(p TA248), we designed a single-tube multiplex PCR based assay for simultaneous detection of all the three major resistance genes and demonstrated the utility of the multiplex marker system in a segregating population. 展开更多
关键词 RICE BACTERIAL blight resistance xa5 xa13 XA21 FUNCTIONAL MARKER multiplex PCR
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CopAB基因突变导致PXO99对铜敏感和致病性降低 被引量:2
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作者 孔令广 巨延虎 +3 位作者 董冉 丁新华 李宁 储昭辉 《植物病理学报》 CAS CSCD 北大核心 2018年第2期176-186,共11页
Cop基因簇是黄单胞菌属抗铜的主要基因位点,而水稻白叶枯病菌PXO99相对其他菌株对铜离子更加敏感。本研究发现抗铜基因Cop AB的6个氨基酸自然缺失突变是造成PXO99对铜离子敏感的主要因素。通过对Cop AB的缺失突变体和恢复抗铜能力的重... Cop基因簇是黄单胞菌属抗铜的主要基因位点,而水稻白叶枯病菌PXO99相对其他菌株对铜离子更加敏感。本研究发现抗铜基因Cop AB的6个氨基酸自然缺失突变是造成PXO99对铜离子敏感的主要因素。通过对Cop AB的缺失突变体和恢复抗铜能力的重组菌株的耐铜实验和接种实验,证实了Cop AB不仅参与黄单胞杆菌的抗铜功能,同时作为一种致病因子参与黄单胞杆菌与水稻的互作。为验证Cop AB基因的功能,从国内白叶枯病菌分离菌株中筛选到4株对铜离子敏感菌株,并证实其Cop AB基因也发生相似的突变。同时,恢复抗铜能力的PXO99互补菌株并不能克服xa13介导的抗性,而分离到的4株铜离子敏感的菌株中,3株不含Pth Xo1的菌株在IR24和IRBB13上致病性相当,说明PXO99对铜离子的敏感性与xa13基因介导的对PXO99专化抗性没有直接的关系。 展开更多
关键词 水稻 白叶枯病 抗铜基因 效应分子 xa13
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