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基因长度多态性导致细胞壁富含脯氨酸的蛋白质出现大小变异。

Genetic length polymorphisms create size variation in proline-rich proteins of the cell wall.

作者信息

Schmidt J S, Lindstrom J T, Vodkin L O

机构信息

Department of Agronomy, University of Illinois, Urbana 61801.

出版信息

Plant J. 1994 Aug;6(2):177-86. doi: 10.1046/j.1365-313x.1994.6020177.x.

DOI:10.1046/j.1365-313x.1994.6020177.x
PMID:7920710
Abstract

Two genes, Prp1 and Prp2, encode proline-rich proteins that are found in different stages of developing seed coats, hypocotyls, and roots of soybeans (Glycine max (L.) Merr.). PRP1 is found in young seed coats and PRP2 is found later during seed desiccation. In some soybean varieties, both proteins are smaller as determined by immunoblotting seed coat proteins separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis. It was found that Prp1 and Prp2 genes are linked to each other by testing seed coat protein extracts from an F2 population of a cross between the cultivar Richland, which exhibits the larger PRP proteins, and Blackhawk, which has the smaller PRP proteins. The Prp1 and Prp2 genes were separated by approximately 13% recombination. Simultaneous expression of soluble PRP2 polypeptides in the maternal seed coat and underlying aleurone layer of the embryo was found. The molecular basis for the size difference between the two varieties was examined using polymerase chain reaction to isolate the Prp genes from Blackhawk, the variety that exhibited the smaller proteins. Both of the genes from Blackhawk contained length polymorphisms that result in omission of some of the repeat units (pro pro val tyr lys) from the proteins. In Prp1, there were two separate deletions in different parts of the gene, each being two tandem repeats in length. In Prp2, there was only one deletion of two tandem repeats. These deletions occur within the coding regions in a manner that conserves the reading frame. The results are the first description of genetic variation in cell wall proteins and its molecular basis.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

两个基因Prp1和Prp2编码富含脯氨酸的蛋白质,这些蛋白质存在于大豆(Glycine max (L.) Merr.)种皮、下胚轴和根发育的不同阶段。PRP1存在于幼嫩种皮中,而PRP2在种子干燥后期出现。在一些大豆品种中,通过免疫印迹法检测经十二烷基硫酸钠聚丙烯酰胺凝胶电泳分离的种皮蛋白,发现这两种蛋白质都较小。通过检测来自品种Richland(其PRP蛋白较大)和Blackhawk(其PRP蛋白较小)杂交的F2群体的种皮蛋白提取物,发现Prp1和Prp2基因相互连锁。Prp1和Prp2基因的重组率约为13%。在母体种皮和胚胎的胚乳层中发现了可溶性PRP2多肽的同时表达。利用聚合酶链反应从表现出较小蛋白质的品种Blackhawk中分离Prp基因,研究了两个品种之间大小差异的分子基础。Blackhawk的两个基因都含有长度多态性,导致蛋白质中一些重复单元(脯氨酸-脯氨酸-缬氨酸-酪氨酸-赖氨酸)缺失。在Prp1中,基因的不同部分有两个单独的缺失,每个缺失长度为两个串联重复。在Prp2中,只有一个两个串联重复的缺失。这些缺失以保持阅读框的方式发生在编码区内。这些结果首次描述了细胞壁蛋白的遗传变异及其分子基础。(摘要截短至250字)

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