首页> 外文期刊>Journal of Phytopathology >Cloning and in silico mapping of resistance gene analogues isolated from rice lines containing known genes for blast resistance.
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Cloning and in silico mapping of resistance gene analogues isolated from rice lines containing known genes for blast resistance.

机译:耐药基因分离的耐药基因类似物的克隆和硅映射。

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摘要

We amplified resistance gene analogues (RGAs) from the genomic DNA of 10 rice lines having varying degree of resistance to Magnaporthe grisea by using degenerate primers and various RGAs were mapped in silico on different rice chromosomes. The amplified products were grouped into 3-8 restriction fragment length polymorphic classes by using Mbo1 and Alu1 restriction enzymes. Of 98 RGAs obtained in this study, 65 RGA clones showed more than 95% homology with various RGAs sequences present in the GenBank. Phylogenetic analysis of these RGAs formed 11 groups. Using sequence homology approach, RGAs isolated in this study were physically mapped on 23 loci on chromosomes 1, 2, 3, 4, 5, 6, 7, 8, 10, 11 and 12. Twenty RGAs were mapped near to the chromosomal regions containing known genes/QTLs for rice blast, bacterial leaf blight and sheath blight resistance. Thirty-nine RGA sequences also contained open reading frame representing signature of potential disease resistance genes..
机译:通过使用退化引物在不同的水稻染色体上映射在不同水稻染色体上的硅映射到MagenaportheGrisea的10种水稻线的基因组DNA的抗性基因类似物(RGA)。 通过使用MBO 1和Alu1限制酶将扩增产物分为3-8个限制性片段长度多态性类别。 在本研究中获得的98例RGA,65个RGA克隆显示出在Genbank中存在的各种RGAS序列的95%同源性。 这些RGA的系统发育分析形成11组。 使用序列同源性方法,本研究中分离的RGA在染色体1,2,3,4,5,6,7,8,10,11和12上物理映射在23个基因座上。二十个RGA被靠近含有含有的染色体区域 用于稻瘟病,细菌叶枯和鞘枯燥的已知基因/ QTL。 三十九个RGA序列还包含了代表潜在疾病抵抗基因签名的开放阅读框架。

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