Blackburn A C, Woollatt E, Sutherland G R, Board P G
Molecular Genetics Group, Division of Molecular Medicine, John Curtin School of Medical Research, Australian National University, Canberra (Australia).
Cytogenet Cell Genet. 1998;83(1-2):109-14. doi: 10.1159/000015145.
The Zeta class of cytosolic glutathione-S-transferases (GSTs) has recently been identified and spans a range of species from plants to humans. The cDNA and protein of a human member of this class have been previously characterised in our laboratory. This cDNA has also been described as maleylacetoacetate isomerase (MAAI), an enzyme of the phenylalanine catabolism pathway (Fernandez-Canon and Penalva, 1998). The present study has determined the structure and chromosome location of the gene encoding human GSTZ1/MAAI. The gene spans approximately 10.9 kb and is composed of 9 exons. Three intron positions of GSTZ1 were precisely conserved compared to the carnation and Caenorhabditis elegans Zeta GST genes. Fluorescent in situ hybridization mapped the gene to a single locus on chromosome 14q24.3, which is in agreement with an independent localization between the Genethon markers D14S263 and D14S67. The coding region of the gene differed from the GSTZ1 cDNA at two nucleotide positions in exon 3, resulting in Lys-32-->Glu and Arg-42--> Gly substitutions. This gene structure information will allow analysis of the polymorphism in genomic DNA samples, and enables further investigations into genetic defects in this step of the phenylalanine catabolism pathway.
胞质谷胱甘肽 - S - 转移酶(GSTs)的Zeta类最近已被鉴定出来,涵盖了从植物到人类的一系列物种。该类人类成员的cDNA和蛋白质先前已在我们实验室中得到表征。这个cDNA也被描述为马来酰乙酰乙酸异构酶(MAAI),它是苯丙氨酸分解代谢途径中的一种酶(费尔南德斯 - 卡农和佩纳尔瓦,1998年)。本研究确定了编码人类GSTZ1 / MAAI的基因的结构和染色体定位。该基因跨度约为10.9 kb,由9个外显子组成。与康乃馨和秀丽隐杆线虫的Zeta GST基因相比,GSTZ1的三个内含子位置精确保守。荧光原位杂交将该基因定位到染色体14q24.3上的一个单一基因座,这与Genethon标记D14S263和D14S67之间的独立定位结果一致。该基因的编码区在外显子3的两个核苷酸位置与GSTZ1 cDNA不同,导致赖氨酸 - 32→谷氨酸和精氨酸 - 42→甘氨酸的替换。这些基因结构信息将有助于分析基因组DNA样本中的多态性,并能够进一步研究苯丙氨酸分解代谢途径这一步骤中的遗传缺陷。