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人类μ类谷胱甘肽S-转移酶基因簇的特征及GSTM1基因缺失

Characterization of the human class Mu glutathione S-transferase gene cluster and the GSTM1 deletion.

作者信息

Xu S, Wang Y, Roe B, Pearson W R

机构信息

Department of Biochemistry, University of Virginia, Charlottesville, Virginia 22908, USA.

出版信息

J Biol Chem. 1998 Feb 6;273(6):3517-27. doi: 10.1074/jbc.273.6.3517.

Abstract

A partial physical map has been constructed of the human class Mu glutathione S-transferase genes on chromosome 1p13.3. The glutathione S-transferase genes in this cluster are spaced about 20 kilobase pairs (kb) apart, and arranged as 5'-GSTM4-GSTM2-GSTM1-GSTM5-3'. This map has been used to localize the end points of the polymorphic GSTM1 deletion. The left repeated region is 5 kb downstream from the 3'-end of the GSTM2 gene and 5 kb upstream from the beginning of the GSTM1 gene; the right repeated region is 5 kb downstream from the 3'-end of the GSTM1 and 10 kb upstream from the 5'-end of the GSTM5 gene. The GSTM1-0 deletion produces a novel 7.4-kb HindIII fragment with the loss of 10.3- and 11.4-kb HindIII fragments. The same novel fragment was seen in 13 unrelated individuals (20 null alleles), suggesting that most GSTM1-0 deletions involve recombinations between the same two regions. We have cloned and sequenced the deletion junction that is produced at the GSTM1-null locus; the 5'- and 3'-flanking regions are more than 99% identical to each other and to the deletion junction sequence over 2.3 kb. Because of the high sequence identity between the left repeat, right repeat, and deletion junction regions, the crossing over cannot be localized within the 2.3-kb region. The 2.3-kb repeated region contains a reverse class IV Alu repetitive element near one end of the repeat.

摘要

已构建出位于1号染色体1p13.3区域的人类μ类谷胱甘肽S-转移酶基因的部分物理图谱。该基因簇中的谷胱甘肽S-转移酶基因彼此间隔约20千碱基对(kb),排列顺序为5'-GSTM4-GSTM2-GSTM1-GSTM5-3'。此图谱已用于定位多态性GSTM1缺失的端点。左侧重复区域位于GSTM2基因3'端下游5 kb处且位于GSTM1基因起始端上游5 kb处;右侧重复区域位于GSTM1基因3'端下游5 kb处且位于GSTM5基因5'端上游10 kb处。GSTM1-0缺失产生一个新的7.4-kb HindIII片段,同时缺失10.3-kb和11.4-kb HindIII片段。在13个无关个体(20个无效等位基因)中观察到相同的新片段,这表明大多数GSTM1-0缺失涉及相同两个区域之间发生的重组。我们已克隆并测序了在GSTM1无效位点产生的缺失连接点;5'和3'侧翼区域彼此之间以及与2.3 kb以上的缺失连接点序列的同源性超过99%。由于左侧重复序列、右侧重复序列和缺失连接点区域之间具有高度的序列同一性,所以交叉互换无法定位在2.3-kb区域内。在该2.3-kb重复区域靠近重复序列一端处含有一个反向IV类Alu重复元件。

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