基于叶绿体DNA的二倍体祖先种面包小麦和硬粒小麦的鉴定

N. Haider, I. Nabulsi
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引用次数: 1

摘要

已被鉴定为栽培多倍体硬粒小麦和面包小麦(Triticum durum L.和T. aestivum L.)基因组供体的物种是培育这两种作物的潜在基因来源。因此,它们的准确识别有助于它们在这些作物的改良中使用。基于叶绿体DNA分析(rpL2和rps16内含子,psbC-trnS, trnT-L和trnL-F),利用聚合酶链反应(PCR- rflp)和限制性片段长度多态性(PCR- rflp), 2018年(AECS分子生物学与生物技术系)尝试从其提出的二倍体祖先物种(即T. monococum, T. urartu, Aegilops speltoides和Ae.)中鉴定硬粒小麦和面包小麦。tauschii)。使用两个PCR标记(psbC-trnS和trnL-F)和三个PCR- rflp位点-酶组合(rps16内含子- tru 1I, rpL2内含子- taq I和trnT-L-Taq I)可以鉴定所有涉及的物种。利用这些候选种特异性cpDNA标记可靠、准确地鉴定硬粒小麦和面包小麦的二倍体祖先,将有助于小麦育种计划、原位和非原位保护工作、商业种子库存中种子纯度的验证,以及确保收集的品种的身份和完整性不会因不必要的基因流动或种子再生后的遗传漂变而改变。
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Identification of Bread and Durum Wheats from their Diploid Ancestral Species Based on Chloroplast DNA
Abstract Species that have been identified as the genome donors to cultivated polyploid durum and bread wheats (Triticum durum L. and T. aestivum L., respectively) are potential gene sources for the breeding of these two crops. Therefore, their accurate identification facilitates their use in the improvement of these crops. Based on chloroplast DNA analysis (rpL2 and rps16 introns, psbC-trnS, trnT-L, and trnL-F) using polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (PCR-RFLP), an attempt was made in 2018 (Department of Molecular Biology and Biotechnology/AECS) to identify durum and bread wheats from each of their proposed diploid ancestral species (i.e., T. monococcum, T. urartu, Aegilops speltoides, and Ae. tauschii). The use of two PCR markers (psbC-trnS and trnL-F) and three PCR-RFLP locus-enzyme combinations (rps16 intron-Tru 1I, rpL2 intron-Taq I, and trnT-L-Taq I) allowed the identification of all species involved. Reliable and accurate identification of diploid ancestors of durum and bread wheats using these candidate species-specific cpDNA markers will be useful for wheat breeding programs, in situ and ex situ conservation efforts, verification of seed purity in commercial seed stocks, and ensuring identity and integrity of accessions held within a collection does not change through unwanted gene flow or by genetic drift after regeneration by seed.
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