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冬小麦麦醇溶蛋白成分的一维聚丙烯酰胺凝胶电泳检测。

Blocks of gliadin components in winter wheat detected by one-dimensional polyacrylamide gel electrophoresis.

机构信息

Institute of General Genetics, USSR Academy of Sciences, Gubkin St. 3, 117809 GSP-1, B-333, Moscow, USSR.

出版信息

Theor Appl Genet. 1984 Apr;67(6):559-68. doi: 10.1007/BF00264904.

Abstract

Inheritance of gliadin components in winter wheat has been studied by one-dimensional polyacrylamide gel electrophoresis. Single F2 grains from 36 intervarietal hybrid combinations have been analysed. The genetic analysis has revealed blocks, including 1-6 gliadin components, which are inherited as individual mendelian traits. About 80 variants of blocks have been detected. On the basis of the allelism test they are grouped into 6 series in accordance with the number of known gliadin-coding loci located on chromosomes of the homoeologous groups 1 and 6. Each series includes 8-18 blocks controlled by different alleles of one gliadin-coding locus. Blocks of components have been confirmed to be inherited codominantly in accordance to the gene dose in the triploid endosperm. The highest similarity between members of one series is observed in groups of blocks controlled by chromosomes ID and 6D. On the contrary, many blocks controlled by chromosomes 1A and 1B have no bands in common. The presented catalogue of blocks of components may be used to make up gliadin genetic formulae and to compare electrophoregrams obtained by different authors. Blocks of gliadin components are suitable genetic markers for use in revealing and studying heterogeneity of wheat varieties, in tracing their origin, in identifying recombinations, translocations and substitutions of the genetic material and in solving many other problems of the origin, evolution and selection of hexaploid wheat.

摘要

利用一维聚丙烯酰胺凝胶电泳研究了冬小麦醇溶蛋白组份的遗传。对来自 36 个品种间杂交组合的 F2 单粒种子进行了分析。遗传分析揭示了醇溶蛋白组份作为单个孟德尔性状遗传的一些区域,包括 1-6 个醇溶蛋白组份。已经检测到大约 80 种组份区域的变异。根据等位基因测试,它们被分成 6 个系列,与位于同源群 1 和 6 染色体上的已知醇溶蛋白编码基因座的数目相对应。每个系列包括 8-18 个由一个醇溶蛋白编码基因座的不同等位基因控制的组份区域。根据三倍体胚乳中的基因剂量,证实了组份区域的遗传是共显性的。在由 ID 和 6D 染色体控制的组份区域的成员之间观察到最高的相似性。相反,由 1A 和 1B 染色体控制的许多组份区域没有共同的条带。所提出的组份区域图谱可用于组成醇溶蛋白遗传公式,并比较不同作者获得的电泳图谱。醇溶蛋白组份区域是合适的遗传标记,可用于揭示和研究小麦品种的异质性,追踪其起源,鉴定遗传物质的重组、易位和替换,以及解决六倍体小麦起源、进化和选择的许多其他问题。

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