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Molecular cytogenetic identification of a wheat-Psathyrostachys huashanica Keng 5Ns disomic addition line with stripe rust resistance

机译:具有条纹抗锈性的小麦-华山芥Keng 5Ns二体组附加系的分子细胞遗传学鉴定

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We developed a new stripe rust resistant line of common wheat-Psathyrostachys huashanica Keng (2n = 2x = 14, NsNs) from a cross between wheat cv. 7182 and P. huashanica via embryo culture, and we refer to this line as 3-8-10-2. We characterized this new line by cytology, genomic in situ hybridization (GISH), EST-SSR, EST-STS, and disease resistance screening. GISH using P. huashanica genomic DNA as the probe indicated that a pair of Ns chromosomes with strong hybridization signals was introduced into 3-8-10-2. We screened 255 EST-SSR and EST-STS multiple-loci markers from seven wheat homoeologous groups in the parent lines. Of these, 90 markers were polymorphic with a polymorphism frequency of 40 %, while two EST-SSR markers and six EST-STS markers located on wheat chromosome group 5 produced specific bands in P. huashanica and 3-8-10-2, respectively. This suggested that the introduced Ns chromosome pair belonged to homoeologous group 5, which was identified using new genome-specific markers. After inoculation with stripe rust isolates, 3-8-10-2 exhibited stripe rust resistance that probably originated from its P. huashanica parent. 3-8-10-2 can be used as a donor source for introducing novel disease resistance genes into wheat during breeding programs with the assistance of molecular and cytogenetic markers. Moreover, 3-8-10-2 had improved agronomic characteristics compared with its parents. Therefore, the addition line could be exploited as an important bridge for wheat breeding and chromosome engineering.
机译:我们从小麦CV的杂交品种中开发了一条新的普通小麦-Psathyrostachys huashanica Keng(2n = 2x = 14,NsNs)条纹抗锈线。 7182和华山假单胞菌通过胚胎培养,我们将该品系称为3-8-10-2。我们通过细胞学,基因组原位杂交(GISH),EST-SSR,EST-STS和抗病性筛选来表征这一新品系。以华山疟原虫基因组DNA为探针的GISH表明,将一对具有强杂交信号的Ns染色体导入3-8-10-2。我们从亲本系的七个小麦同源群体中筛选了255个EST-SSR和EST-STS多基因座标记。其中90个标记是多态性,多态性频率为40%,而位于小麦第5组染色体上的两个EST-SSR标记和六个EST-STS标记分别在华山对虾和3-8-10-2处产生特异性条带。 。这表明引入的Ns染色体对属于同源组5,其使用新的基因组特异性标记鉴定。接种条锈菌分离株后,3-8-10-2表现出条锈病抗性,该抗性可能源自其华山对虾。 3-8-10-2可作为供体来源,在育种程序中借助分子和细胞遗传标记将新的抗病基因引入小麦。此外,与亲本相比,3-8-10-2具有更好的农艺特性。因此,该附加系可作为小麦育种和染色体工程的重要桥梁。

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