McLellan L I, Kerr L A, Cronshaw A D, Hayes J D
Department of Clinical Chemistry, University of Edinburgh, Royal Infirmary, U.K.
Biochem J. 1991 Jun 1;276 ( Pt 2)(Pt 2):461-9. doi: 10.1042/bj2760461.
Liver cytosol from mice fed on a normal diet contains Alpha-class glutathione S-transferase (GST) subunits of Mr 25,800, Mu-class GST subunits of Mr 26,400 and Pi-class GST subunits of Mr 24,800. Feeding female mice with a diet containing the anticarcinogenic antioxidant butylated hydroxyanisole (BHA) causes induction of the constitutively expressed Mu-class and Pi-class subunits. BHA also induces an Alpha-class GST comprising subunits of Mr 25,600, which is not expressed at detectable levels in normal mouse liver [McLellan & Hayes (1989) Biochem. J. 263, 393-402]. Data are now presented that show that administration of the anticarcinogen beta-naphthoflavone (BNF), like BHA, induces the Alpha-class 25,600-Mr subunits but not the constitutive Alpha-class GST with subunits of Mr 25,800. The effects of BNF on expression of hepatic GST were studied in both DBA/2 and C57BL/6 mice; these studies revealed a preferential induction of the Alpha-class 25,600-Mr subunits and of the Pi-class 24,800-Mr subunits in those mice in possession of a functional Ah receptor. The BHA/BNF-inducible Alpha-class GST can be resolved into two separate, non-interconvertible peaks by reverse-phase h.p.l.c. Automated amino acid sequence analysis of CNBr-derived peptides from each of these h.p.l.c.-purified peaks showed that the peaks contained at least two very similar subunits. These have been named Ya1 and Ya2. The amino acid sequence of the Ya1 subunit was compared with sequences deduced from a genomic clone, lambda mYa1 (Daniel, Sharon, Tichauer & Sarid (1987) DNA 6, 317-324], and a cDNA clone, pGT41 [Pearson, Reinhart, Sisk, Anderson & Adler (1988) J. Biol. Chem. 263, 13324-13332]. Our data suggest that the Ya1 subunit represents the subunit encoded by the genomic clone, lambda mYa1. Sequence analysis of the constitutive Alpha-class Ya3 subunit (Mr 25,800) shows that, although it is a member of the same gene family as the Ya1 and Ya2 subunits, it represents a distinct sub-family of Alpha-class GST, containing subunits that are more similar to rat Yc. Our data indicate that, of these Alpha-class GST subunits, the two with Mr 25,600 (Ya1 and Ya2) are selectively induced by BHA or BNF in mouse liver; neither BHA nor BNF induces significantly the GST subunit with Mr 25,800 (Ya3).
以正常饮食喂养的小鼠肝脏胞液中含有分子量为25,800的α类谷胱甘肽S-转移酶(GST)亚基、分子量为26,400的μ类GST亚基和分子量为24,800的π类GST亚基。用含有抗癌抗氧化剂丁基羟基茴香醚(BHA)的饮食喂养雌性小鼠,会诱导组成型表达的μ类和π类亚基。BHA还诱导出一种由分子量为25,600的亚基组成的α类GST,在正常小鼠肝脏中该亚基表达水平极低,无法检测到[麦克莱伦和海斯(1989年)《生物化学杂志》263卷,393 - 402页]。现在有数据表明,给予抗癌剂β-萘黄酮(BNF),与BHA一样,会诱导分子量为25,600的α类亚基,但不会诱导分子量为25,800的组成型α类GST亚基。在DBA/2和C57BL/6小鼠中研究了BNF对肝脏GST表达的影响;这些研究表明,在具有功能性Ah受体的小鼠中,分子量为25,600的α类亚基和分子量为24,800的π类亚基受到优先诱导。通过反相高效液相色谱法,可将BHA/BNF诱导的α类GST分离为两个独立的、不可相互转换的峰。对来自这些高效液相色谱纯化峰的每个峰的溴化氰衍生肽进行自动氨基酸序列分析表明,这些峰至少包含两个非常相似的亚基。它们被命名为Ya1和Ya2。将Ya1亚基的氨基酸序列与从基因组克隆λmYa1(丹尼尔、沙龙、蒂乔尔和萨里德(1987年)《DNA》6卷,317 - 324页]和cDNA克隆pGT41[皮尔逊、莱因哈特、西斯克、安德森和阿德勒(1988年)《生物化学杂志》263卷,13324 - 13332页]推导的序列进行了比较。我们的数据表明,Ya1亚基代表基因组克隆λmYa1编码的亚基。组成型α类Ya3亚基(分子量为25,800)的序列分析表明,尽管它与Ya1和Ya2亚基属于同一基因家族,但它代表α类GST的一个独特亚家族,其包含的亚基与大鼠Yc更相似。我们的数据表明,在这些α类GST亚基中,分子量为25,600的两个亚基(Ya1和Ya2)在小鼠肝脏中被BHA或BNF选择性诱导;BHA和BNF均未显著诱导分子量为25,800的GST亚基(Ya3)。