首页> 外文会议>International Wheat Genetics Symposium >Genetic analysis of two genes for vernalization response, the former Vrn2 and Vm4, by using PGR based molecular markers.
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Genetic analysis of two genes for vernalization response, the former Vrn2 and Vm4, by using PGR based molecular markers.

机译:基于PGR的分子标记,通过基于PGR的分子标记对络合响应,前VRN2和VM4的两个基因的遗传分析。

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For genetical analysis of genes for vernalization response in wheat, formerly designated as Vrn2, molecular markers closely linked to the Vrn-1 gene family were analyzed by using NILs of "Triple Dirk". At Xwg644-5B, SNP (C/T) was detected between TD(B) carrying Vrn2 and TD(C) carrying vrn2, and dCAPS was successfully detected between two NILs. The analysis of a BF_2 population (TD(B)//TD(C) revealed close linkage (1.7 cM) between WG644-5B and Vrn2. Close linkage between Vrn2 and a SSR locus Xgwm408 was also confirmed (2.5cM). It was therefore concluded that the former Vrn2 is located on chromosome 5B and equivalent to Vrn-Bl. For Vrn4, it was located on 5D by monosomic analysis, and thus SSR markers mapped on chromosome 5D was analyzed, and close linkage (4.5cM) was detected between Vrn4 and a SSR locus Xgdm3. It was therefore concluded that Vrn4 is located on the proximal part of SDL and independent of Vrn-Dl located on the distal part of 5DL. Since no genes or QTLs controlling vernalization response have so far been reported in this region of homoeologous chromosome 5, it can be considered as a new class of vernalization gene which should be designated as Vrn-D5.
机译:对于小麦的葡萄化响应基因的基因分析,以前指定为VRN2,通过使用“三重德克”的含量分析与VRN-1基因家族密切相关的分子标记。在XWG644-5B中,在携带VRN2的TD(B)和携带VRN2的TD(B)之间检测SNP(C / T),并且在两种NIL之间成功检测到DCAP。对BF_2群体的分析(Td(b)// td(c)显示WG644-5B和VRN2之间的紧密连锁(1.7cm)。VRN2和SSR基因座XGWM408之间的紧密连锁也被证实(2.5cm)。它是因此,前VRN2位于染色体5B上并等同于VRN-BL。对于VRN4,它通过单体分析位于5D,因此分析了映射在染色体5D上的SSR标记,并检测到紧密的连接(4.5cm) VRN4和SSR基因座XGDM3之间。因此,VRN4位于SDL的近端部分,并且独立于位于5dl的远端部分上的VRN-DL。由于到目前为止,迄今为止还没有控制控制vernalization响应的基因或QTLS。该区域的阳性染色体5,它可以被认为是应该被指定为VRN-D5的新类含量基因。

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