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Identification of Bread and Durum Wheats from their Diploid Ancestral Species Based on Chloroplast DNA

机译:基于叶绿体DNA的二倍体祖先物种鉴定面包和杜兰姆小麦

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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.
机译:已被鉴定为培养多倍体硬粒和面包小麦的基因组供体的物种(分别是小麦的面包小麦(Triticum Durum L.和T. aestivum L.)是用于繁殖这两种作物的潜在基因来源。因此,他们的准确识别有助于它们在改善这些作物的过程中。基于叶绿体DNA分析(RPL2和RPS16内含子,PSBC-TRNS,TRNT-L和TRNL-F)使用聚合酶链反应(PCR)和PCR限制性片段长度多态性(PCR-RFLP),在2018年进行了尝试(分子生物学和生物技术/ AECS)以鉴定来自其提出的二倍体祖先物种中的每种杜兰姆和面包小麦(即,T. monococcum,T.ureartu,Aegilops Spottoides和Ae。Tauschii)。使用两种PCR标记物(PSBC-TRNS和TRNL-F)和三种PCR-RFLP基因座酶组合(RPS16 Intron-TRU 1I,RPL2 Intron-Taq I和TRNT-L-TAQ I)允许识别所有涉及的物种。使用这些候选物种特异性CPDNA标记可靠和准确地识别多水肿和面包小麦的二倍体祖先将是对小麦养殖计划,原位和前所保护努力,验证商业种子股中的种子纯度,并确保身份和完整性在收集中持有的含量不会通过未量的基因流或通过种子再生后通过遗传漂移而改变。

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