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Marker-assisted backcross breeding in wheat.

机译:标记辅助的小麦回交育种。

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Restriction fragment length polymorphism (RFLP) markers can be converted to sequence-tagged-site (STS) primer sets recognized by the polymerase chain reaction (PCR). STS-PCR markers were mapped in wheat and barley to evaluate the correspondence of chromosome locations between species and with the mapped RFLPs. STS amplification products in wheat mapped to the same chromosome as the RFLP approximately 70% of the time. Barley STS location corresponded to the RFLP location approximately 60% of the time. RFLP mapping information was transferable 82% of the time between wheat and barley with STS information transferable 74% of the time. Multiple STS locations were generally mapped in wheat. Southern analysis was used to evaluate the homology of the amplification products to the RFLP clone. Homologous sequences were generally amplified, but non-homologous sequences were also amplified in some cases. The results indicate that STS information can be transferred between wheat and barley, and that RFLP location could provide an indication of the STS location in both wheat and barley. However, amplification of unmapped RFLP locations and non-homologous sequences is a factor to consider in their application.; The potential of STS markers as an aid in selection for the recurrent parent in a backcross breeding program to introgress Russian wheat aphid resistance into wheat was also investigated. Three recombinant inbred populations were established from crosses between a Russian wheat aphid resistant line, PI372129, and two Montana hard red spring wheat cultivars, Pondera and Newana, in order to evaluated the level of donor genome and potential correlations with phenotypic performance. The percentage of donor genome, based on marker analysis, varied between the lines within the populations. Significant positive correlations between percentage of donor genome with plant height and straw strength were observed for the Pondera single cross population. No significant correlations were observed for the two backcross populations. The backcross population means approached that of the recurrent pattern with a decrease in the number of lines significantly different from the recurrent parent. Results suggests that molecular marker could be used to select for the recurrent parent genotype, and provide optimism for marker-assisted selection to recover the recurrent parent phenotype.
机译:限制性片段长度多态性(RFLP)标记可以转换为通过聚合酶链反应(PCR)识别的序列标记位点(STS)引物组。将STS-PCR标记在小麦和大麦中作图,以评估物种之间的染色体位置以及所映射的RFLP的对应性。小麦中的STS扩增产物大约70%的时间映射到与RFLP相同的染色体。大麦STS位置对应于RFLP位置的时间约为60%。 RFLP映射信息可在小麦和大麦之间转移82%的时间,而STS信息可转移74%的时间。通常在小麦中绘制了多个STS位置。 Southern分析用于评估扩增产物与RFLP克隆的同源性。通常扩增同源序列,但是在某些情况下也扩增非同源序列。结果表明,STS信息可以在小麦和大麦之间传递,并且RFLP位置可以提供小麦和大麦中STS位置的指示。然而,未映射的RFLP位置和非同源序列的扩增是在其应用中要考虑的因素。还研究了STS标记在回交育种计划中选择轮回亲本以将俄罗斯小麦蚜虫抗性引入小麦的潜力。从俄罗斯小麦蚜虫抗性品系PI372129与两个蒙大拿州硬红春小麦品种Pondera和Newana之间的杂交中建立了三个重组近交种群,以评估供体基因组水平和与表型表现的潜在相关性。基于标记分析,供体基因组的百分比在群体内的品系之间变化。 Pondera单杂交种群的供体基因组百分比与株高和稻草强度之间存在显着的正相关。没有观察到两个回交群体的显着相关性。回交群体的平均值接近轮回模式的平均值,但行数的减少与轮回亲本的差异显着。结果表明,分子标记物可用于选择复发亲本基因型,并为标记物辅助选择提供乐观,以恢复复发亲本表型。

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