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HRM technology for the identification and characterization of INDEL and SNPs mutations in genes involved in drought and salt tolerance of durum wheat

机译:HRM技术用于硬粒小麦抗旱耐盐基因中INDEL和SNPs突变的鉴定与表征

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摘要

WRKY transcription factors are one of the largest families of transcriptional regulators and form an integral part of signalling webs which modulate many plant processes, such as abiotic stress tolerance. In the present paper, an innovative method has been applied to identify novel WRKY-1 alleles involved in the responses to salt and drought stresses in Triticum durum.This technique involves scanning for sequencing variations in cDNA-derived PCR amplicons, using high-resolution melting (HRM) followed by direct Sanger sequencing of only those amplicons which were predicted to carry nucleotide changes. HRM represents a novel advance in detection of single-nucleotide polymorphisms (SNPs) by measuring temperature-induced strand separation of short PCR amplicons. The use of this approach is still limited in the field of plant biology. Here, HRM analysis has been applied to the discovery and genotyping of durum wheat SNPs. Specific primers have been designed, starting at multi-alignment ofWRKY-1-conserved portions. The PCR amplicons, containing single SNPs, produce distinctive HRM profiles, and by sequencing the PCR products identified, SNPs have been characterized and validated. The results showed that all the revealed SNPs are located on salt-tolerant varieties, confirming their value in breeding activities.
机译:WRKY转录因子是最大的转录调节子家族之一,并构成信号网的组成部分,该信号网可调节许多植物过程,例如非生物胁迫耐受性。在本文中,一种创新的方法已被用于鉴定与硬粒小麦对盐和干旱胁迫的响应有关的新型WRKY-1等位基因,该技术涉及使用高分辨率熔解技术扫描cDNA衍生的PCR扩增子的测序变异。 (HRM),然后仅对那些预期携带核苷酸变化的扩增子进行直接Sanger测序。 HRM通过测量温度引起的短PCR扩增子的链分离,代表了单核苷酸多态性(SNP)检测的新进展。在植物生物学领域,这种方法的使用仍然受到限制。在这里,HRM分析已应用于硬质小麦SNP的发现和基因分型。从WRKY-1保守部分的多重比对开始,已经设计了特异性引物。包含单个SNP的PCR扩增子可产生独特的HRM图谱,通过对鉴定出的PCR产物进行测序,可以对SNP进行表征和验证。结果表明,所有揭示的SNP都位于耐盐品种上,证实了其在育种活动中的价值。

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