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两个编码玉米谷胱甘肽S-转移酶(GST I和GST II)的基因的分子分析与定位

Molecular analysis and mapping of two genes encoding maize glutathione S-transferases (GST I and GST II).

作者信息

Rossini L, Pè M E, Frova C, Hein K, Sari-Gorla M

机构信息

Department of Genetics and Microbiology, University of Milan, Italy.

出版信息

Mol Gen Genet. 1995 Sep 20;248(5):535-9. doi: 10.1007/BF02423448.

Abstract

Maize glutathione S-transferase (GST) isozymes are encoded by a gene family comprising at least five genes, three of which (Gst I, II and III) have recently been isolated and sequenced. The enzymes are active as homo or heterodimers and exhibit intraspecific polymorphism including a "null" variant for the two major isoforms expressed in roots. Northern blot analyses performed on total root RNA from "null" and "plus" genotypes, using Gst I- and Gst II-specific probes, indicated that the Gst I gene controls the expression of the two major GST isoforms expressed in roots. Gst I and Gst II were mapped by RFLP analysis using an F2 population of 149 individuals previously characterized. Gst I was localized on the long arm of chromosome 8, while two putative Gst II loci were mapped to chromosome 8 (70 cM from Gst I) and 10, respectively.

摘要

玉米谷胱甘肽S-转移酶(GST)同工酶由一个至少包含五个基因的基因家族编码,其中三个基因(Gst I、II和III)最近已被分离并测序。这些酶以同源或异源二聚体形式具有活性,并表现出种内多态性,包括在根中表达的两种主要同工型的“无效”变体。使用Gst I和Gst II特异性探针,对“无效”和“加性”基因型的总根RNA进行的Northern印迹分析表明,Gst I基因控制根中表达的两种主要GST同工型的表达。使用先前鉴定的149个个体的F2群体,通过RFLP分析对Gst I和Gst II进行定位。Gst I定位在8号染色体的长臂上,而两个假定的Gst II基因座分别定位到8号染色体(距Gst I 70 cM)和10号染色体。

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