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Fine mapping of a major wheat QTL for Fusarium head, blight resistance

机译:精细映射镰刀菌头的主要小麦QTL,耐受抗性

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A major QTL, Qfhs.ndsu-SBS, for resistance to Fusarium head blight (FFffi) in wheat has been identified and verified by several research groups. The objectives of this study were to develop STS (sequence-tagged site) markers from wheat ESTs homologousto the corresponding genomic sequences of rice, and to construct a high resolution map of the Qfhs.ndsu-SBS region. The sequences of PI-derived artificial chromosome (PAC)/bacterial artificial chromosome (BAC) clones covering the sub-distal portion of rice chromosome 1S were used as queries for BLASTN search to identify wheat ESTs most likely near Qfhs.ndsu-SBS. Sixty-eight out of 79 STS primer pairs designed from wheat ESTs amplified PCR products from the genomic DNA of wheat cultivar 'Chinese Spring'. Twenty-eight STS markers were localized on chromosome 3BS by aneuploid analysis. Six out of the nine STS markers mapped in the Sumai 3/Stoa population had higher i?" and LOD values for this QTL than the most significant marker reported previously. Sixteen hundred F2 plants derived from a single F7 plant heterozygous for the Qfhs.ndsu-SBS region were screened for recombinants with two SSR markers, gwm533 and gwm493, and 192 recombinants were identified. Five STS markers and two additional SSR markers were used to genotype the 192 recombinants, and a fine genetic map was constructed. Homozygous recombinants were identified in the F3 generation, and F4 seeds will be used for phenotypic analysis of FHB reaction to precisely locate Qfhs.ndsu-SBS to a narrow marker interval.
机译:一个主要的QTL,Qfhs.ndsu-SBS,用于在小麦赤霉病(FFffi)电阻已被确定,并通过几个研究小组证实。本研究的目标是制定STS(序列标记位点)从小麦的EST标记物homologousto大米的相应的基因组序列,并构建Qfhs.ndsu-SBS区域的高分辨率图。 PI衍生的人工染色体(PAC)/细菌人工染色体(BAC)克隆覆盖水稻染色体1S的子远端部分的序列用作用于BLASTN搜索查询向最有可能识别邻近Qfhs.ndsu-SBS小麦EST序列。从小麦EST序列设计的六十八出的79 STS引物对PCR扩增产物从小麦品种“中国春”的基因组DNA。二十八个STS标记分别定位于通过非整倍体染色体分析3BS。六出在苏麦3号/柱廊人口映射九个STS标记有较高的我吗?”这个QTL比最显著标记LOD值先前报道,从单一的F7植物杂衍化为Qfhs.ndsu一千六百F2植物-SBS区域进行了筛选具有两个SSR标记,gwm533和gwm493,和192点的重组体的重组体进行鉴定。五个STS标记和两个附加SSR标记用于基因分型的192个重组体,构建一个细遗传图谱。鉴定纯合的重组体在F3代,和F4种子将被用于FHB反应的表型分析,以精确地定位Qfhs.ndsu-SBS到窄标记间隔。

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