Zhong S, Spurr N K, Hayes J D, Wolf C R
ICRF Molecular Pharmacology Group, Edinburgh, Scotland.
Biochem J. 1993 Apr 1;291 ( Pt 1)(Pt 1):41-50. doi: 10.1042/bj2910041.
The Mu-Class glutathione S-transferases (GSTs) are subject to marked inter-individual variation in man, owing to the fact that 40-50% of the population fail to express M1 subunits. Mu-Class GST from two lymphoblastoid cell lines (expressing M1 subunits and the other 'nulled' for M1) have been studied. Both cell lines were found to express a Mu-Class GST that has not been described previously. The cDNA encoding this novel transferase, designated 'GSTM4' has been isolated and the enzyme shown to be comprised of 218 amino acids (including the initiator methionine residue) with an M(r) of approx. 25.5 kDa. Molecular cloning demonstrated that the lymphoblastoid cell line which expressed GSTM1 possessed the b allelic variant (i.e. that with an asparagine residue at position 173). The genes for GSTM4 and GSTM1b have been cloned and found to contain seven introns and eight exons. The coding region of the GSTM4 gene, including the seven introns, encompasses 5.0 kb, whereas the same region of GSTM1b is 5.5 kb; the difference in the size of the two genes is due to the length of intron 7. DNA sequencing allowed a GSTM4-gene-specific oligo-primer to be designed which has been utilized in a PCR-based assay to determine that the GSTM4 gene is located on chromosome 1.
μ类谷胱甘肽S-转移酶(GSTs)在人类个体间存在显著差异,因为40%-50%的人群无法表达M1亚基。对来自两个淋巴母细胞系的μ类GST(一个表达M1亚基,另一个M1亚基“缺失”)进行了研究。发现这两个细胞系均表达一种此前未被描述过的μ类GST。编码这种新型转移酶(命名为“GSTM4”)的cDNA已被分离出来,该酶由218个氨基酸组成(包括起始甲硫氨酸残基),分子量约为25.5 kDa。分子克隆表明,表达GSTM1的淋巴母细胞系具有b等位基因变体(即第173位为天冬酰胺残基的变体)。GSTM4和GSTM1b的基因已被克隆,发现它们都含有7个内含子和8个外显子。GSTM4基因的编码区(包括7个内含子)长度为5.0 kb,而GSTM1b的同一区域为5.5 kb;这两个基因大小的差异是由于内含子7的长度不同。DNA测序使得能够设计出一种GSTM4基因特异性寡核苷酸引物,该引物已被用于基于PCR的分析中,以确定GSTM4基因位于1号染色体上。