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首页> 外文期刊>Fresenius environmental bulletin >IDENTIFICATION OF A LEAF RUST RESISTANCE GENE Lr24 IN THE BREAD WHEAT (TRITICUM AESTIVUM L.) GENOTYPES
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IDENTIFICATION OF A LEAF RUST RESISTANCE GENE Lr24 IN THE BREAD WHEAT (TRITICUM AESTIVUM L.) GENOTYPES

机译:面包小麦(Triticum Aestivum L.)基因型鉴定叶片锈病基因LR24

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One of the most important pathogens of wheat is leaf rust caused by Puccinia triticina (syn. Puc- cinia recondita Rob. ex Desm. f.sp. tritici). It causes important yield decreases in bread wheat, mainly in the years with a high infection pressure of the pathogen. DNA marker-assisted selection (MAS) have been used for the identification of leaf rust (Lr) resistance genes into adapted commercial winter wheat cultivars and bred lines. 2 F1 hybrids, 2 Thatcher line and 14 cultivar which are used commonly in Turkey and have never been idenitify for resistance against leaf rust by SSR marker linked to the Lr24 gene. The SSR marker linked to resistance gene Lr24 was robust and highly specific for these gene and will be useful in marker-assisted selection in wheat. Markers for resistance gene, Lr24 was identified in laboratory as amplification products of 310 bp, respectively. Serial PCR experiments were carried out for determination of optimal PCR conditions for Lr24 gene in our labrotary. PCR conditions were as follows: 5 min at 94°C, followed by 40 cycles of I min at 94°C, I min 62°C depending on the primer combination, and I min at 72°C. The last step was incubation for 10 min at 72°C. The primers used in the PCR runs were as follows: After analyzed 18 genotypes, Lr24 gene was not detected except Thatcher Lr24 (positive control line).
机译:小麦最重要的病原体之一是普昔锡尸体引起的叶子锈病(SYN。PUC- CINIA RECORDITA ROB.EXSM.F.SP.TRITCI)。它导致面包小麦的重要产量下降,主要是在多年来病原体感染压力的年份。 DNA标记辅助选择(MAS)已被用于鉴定叶片生锈(LR)抗性基因进入适应的商业冬小麦品种和繁殖线。 2 F1杂种,2个撒切尔线和14种含有在土耳其中使用的14种品种,从未通过链接到LR24基因的SSR标记对叶片生锈的抗性的抗性。链接到抗性基因LR24的SSR标记对于这些基因具有稳健且高度特异性,并且可用于小麦的标记辅助选择。抗性基因的标记分别以310bp的扩增产物在实验室中鉴定出LR24。进行连续PCR实验,用于测定我们的腰果中LR24基因的最佳PCR病症。 PCR条件如下:在94℃下5分钟,然后在94℃下的40分钟循环,Im min 62℃,取决于引物组合,Imin在72℃下。在72℃下,将最后一步孵育10分钟。在PCR运行中使用的引物如下:除了分析18个基因型后,除了茅草LR24(阳性对照线)外未检测到LR24基因。

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