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首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >Multi-locus DNA fingerprinting and genetic diversity in jute (Corchorus spp.) based on sequence-related amplified polymorphism
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Multi-locus DNA fingerprinting and genetic diversity in jute (Corchorus spp.) based on sequence-related amplified polymorphism

机译:基于序列相关扩增多态性的黄麻(Corchorus spp。)多基因座DNA指纹图谱和遗传多样性

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Sequence-Related Amplified Polymorphism (SRAP) markers were used for genetic diversity assessment and cultivar identification among 31 cultivars of jute belonging to two cultivated species Corchours olitorius L. and C. capsularis L. Forty-three primer-pairs produced a total of 394 bands with an average of 9 bands per primer pair and 89% bands were polymorphic across the genotypes of two species. Average genetic diversity in the cultivars of C. olitorius and C. eapsularis was 7.2% (range 2.8-12.3%) and 7.6% (range 2.2-13.1%), respectively. Jute cultivars JRC 698, JRC 7447, TJ 40, S19 and JRO 3690 were more diverse compared to rest of the cultivars. UPGMA cluster analysis grouped all cultivars into two clusters which were representative of C. olitorius and C. capsularis species. All the cultivars could be unequivocally differentiated from one another based on the pooled profile of 43 primer-pairs, however, 24 of 31 cultivars could be identified uniquely. The probability of chance identity of any twocultivars based on SRAP markers was very low and was 6.95 x 10~(-07) and 2.23 x 10~(-07) for cultivars of C. capsularis and C. olitorius, respectively. Primer-pairs EM1-ME5, EM4-ME1, EM8-ME1 and EM10-ME1 were found to be useful for genetic diversity andcultivar identification. Our results show that SRAP markers could be effectively used for genetic diversity analyses in jute. For poor genetic diversity and resulting narrow genetic base, these markers will prove to be highly useful for identifying elitegermplasm in a jute breeding program.
机译:使用序列相关的扩增多态性(SRAP)标记对属于两个栽培种Corchours olitorius L.和荚膜梭菌L.的31个黄麻品种进行遗传多样性评估和品种鉴定。43个引物对共产生394条带每个引物对平均有9个条带,两个物种的基因型之间有89%的条带是多态的。少毛隐孢子虫和小球隐孢子虫的平均遗传多样性分别为7.2%(范围为2.8-12.3%)和7.6%(范围为2.2-13.1%)。与其余品种相比,黄麻品种JRC 698,JRC 7447,TJ 40,S19和JRO 3690更具多样性。 UPGMA聚类分析将所有品种分为两个聚类,分别代表少毛隐孢子虫和荚膜隐孢子虫种。根据43个引物对的汇总,可以明确区分所有品种,但是,可以唯一地鉴定31个品种中的24个。基于SRAP标记的任何两个品种的机会同一性的概率非常低,荚膜梭菌和寡核梭菌的品种分别为6.95 x 10〜(-07)和2.23 x 10〜(-07)。发现引物对EM1-ME5,EM4-ME1,EM8-ME1和EM10-ME1可用于遗传多样性和品种鉴定。我们的结果表明,SRAP标记可以有效地用于黄麻的遗传多样性分析。对于较差的遗传多样性和由此产生的狭窄遗传基础,这些标记物将被证明对鉴定黄麻育种计划中的优良种质非常有用。

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