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Inter- and intra-population genetic variations in Jatropha curcaspopulations revealed by inter-simple sequence repeat molecularmarkers

机译:简单序列重复分子标记揭示麻风树麻疯树种群内和种群内的遗传变异

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Inter simple sequence reaction (ISSR) was employed to assess diversity in six Jatropha populations that were collectedin Malaysia, Indonesia, the Philippines and India. A total of 144 accessions (24 accessions per population)were selected and analysed with 10 ISSR primer combinations to generate a total of 143 polymorphic fragments.The number of bands generated per primer varied from 4 to 27. The percentages of polymorphic bands for theIndonesia1, Indonesia2, Malaysia1, Malaysia2, Philippines and India Jatropha populations were 54.6, 59.4, 46.2,53.2, 60.8 and 56.4%, respectively, with an average of 55.1%. The Nei’s total genetic diversity (HT), the intra-populationsgenetic diversity (HS) and the coefficient of genetic differentiation (GST) were 0.1136, 0.0989 and 0.1295,respectively. The coefficient of genetic differentiation (GST) was 0.1295, which indicated a frequency of approximately13% in genetic variations observed in the inter-Jatropha populations, while an 87% variation correspondedto the intra-Jatropha populations. Analysis of molecular variance (AMOVA) analysis indicated highly significant (p ≤0.001) genetic differences among the six Jatropha populations. An UPGMA dendrogram was constructed, and theJatropha populations were grouped into four major clusters at a coefficient level of 0.28. The genetic similaritiesbetween the populations ranged from 0.31 to 0.25. The principal component analysis showed a relatively similargrouping of the populations. To obtain high heterotic responses, hybridisation should be made between the twodistant populations of Malaysia 1 and Indonesia1.
机译:使用简单序列间反应(ISSR)评估了在马来西亚,印度尼西亚,菲律宾和印度收集的六个麻疯树种群的多样性。总共选择了144个种质(每个种群24个种质),并用10种ISSR引物组合进行分析,以产生143个多态性片段。每个引物产生的条带数量从4到27不等。印度尼西亚2,马来西亚1,马来西亚2,菲律宾和印度的麻风树种群分别为54.6%,59.4%,46.2、53.2、60.8和56.4%,平均为55.1%。 Nei的总遗传多样性(HT),种群内遗传多样性(HS)和遗传分化系数(GST)分别为0.1136、0.0989和0.1295。遗传分化系数(GST)为0.1295,表明在麻疯树间种群中观察到的遗传变异频率约为13%,而87%的变异对应于麻疯树内种群。分子变异分析(AMOVA)分析表明,六个麻疯树种群之间的遗传差异非常显着(p≤0.001)。构造了一个UPGMA树状图,并将麻风树属种群分为四个主要簇,系数水平为0.28。种群之间的遗传相似性在0.31至0.25之间。主成分分析表明,人群的分组相对相似。为了获得高异质性反应,应该在马来西亚1和印度尼西亚1的两个远距离种群之间进行杂交。

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