Johnson J A, Finn K A, Siegel F L
Environmental Toxicology Center, University of Wisconsin, Madison 53706.
Biochem J. 1992 Feb 15;282 ( Pt 1)(Pt 1):279-89. doi: 10.1042/bj2820279.
Glutathione S-transferases (GSTs) were isolated from rat liver, lung, heart, kidney, testis and brain by coupled affinity chromatography and subunits were resolved by reverse-phase h.p.l.c. The reverse-phase h.p.l.c. technique was improved from our previously published work [Johnson, Neal, Collins & Siegel (1990) Biochem. J. 270, 483-489] by changing from a C4 to a C18 wide-pore reverse-phase column; this resulted in baseline or near-baseline resolution of all GST subunits. There were significant tissue-dependent differences in the expression of GST subunits and the level of GST subunits present was quantitatively determined for each of the tissues. The extent of methylation of GSTs in vitro and distribution of GST methyltransferase (GST-MT) was determined in cytosolic fractions from each of these tissues. Purified GST isoenzymes were methylated with partially purified liver GST-MT. Methylation of Mu class subunits 3 and 4, the preferred substrates of methylation in liver, was substoichiometric in all tissues. The extent of methylation of subunit 3 ranged from 0.13% to 0.94% and subunit 4 from 0.03% to 0.60%. Methylation of Alpha class subunits was either not detectable or 5-10-fold less than that of Mu class subunits 3 and 4. Pi class subunit 7 was methylated to a greater extent than the Alpha class subunits but less than Mu class isoenzymes. A notable exception to this low level of methylation was GST 11-11, found mainly in testis and brain. Methylation of subunit 11 reached 21.9% (219 pmol of methyl group/nmol of subunit 11) when this isoenzyme was incubated with partially purified liver GST methyltransferase. Methylation of GST 11-11 was found to inhibit the conjugating activity of this isoenzyme towards 1-chloro-2,4-dinitrobenzene; the degree of inhibition of conjugating activity correlated with the extent of methylation of GST 11-11. GST-MT activity toward GST subunits 3, 4 and 11 was present in kidney and liver, detectable in lung and heart, but absent from brain and testis. Anion-exchange chromatography of GST-MTs from liver and kidney suggested the presence of four different forms of GST-MT (I-IV) and indicated that GST-MT isoenzymes III and IV were present at significantly lower concentrations in kidney than liver. The present paper shows that methylation is an enzyme-catalysed reaction that differs in substrate-specificity with respect to different GST isoenzymes, that expression of GST-MT is tissue-dependent and multiple forms of the enzyme are present in liver and kidney, and that methylation inhibits GST activity.(ABSTRACT TRUNCATED AT 400 WORDS)
通过偶联亲和层析从大鼠肝脏、肺、心脏、肾脏、睾丸和大脑中分离出谷胱甘肽S-转移酶(GSTs),并通过反相高效液相色谱法分离亚基。反相高效液相色谱技术在我们之前发表的工作[约翰逊、尼尔、柯林斯和西格尔(1990年)《生物化学杂志》270卷,483 - 489页]基础上进行了改进,从C4反相柱改为C18宽孔反相柱;这使得所有GST亚基都实现了基线或接近基线的分离。GST亚基的表达存在显著的组织依赖性差异,并且对每个组织中GST亚基的含量进行了定量测定。测定了这些组织的胞质部分中GSTs的体外甲基化程度以及GST甲基转移酶(GST-MT)的分布。用部分纯化的肝脏GST-MT对纯化的GST同工酶进行甲基化。Mu类亚基3和4是肝脏中甲基化的首选底物,在所有组织中其甲基化均为亚化学计量。亚基3的甲基化程度在0.13%至0.94%之间,亚基4在0.03%至0.60%之间。Alpha类亚基的甲基化要么无法检测到,要么比Mu类亚基3和4低5 - 10倍。Pi类亚基7的甲基化程度高于Alpha类亚基,但低于Mu类同工酶。这种低甲基化水平的一个显著例外是主要存在于睾丸和大脑中的GST 11 - 11。当该同工酶与部分纯化的肝脏GST甲基转移酶一起孵育时,亚基11的甲基化达到21.9%(219皮摩尔甲基/纳摩尔亚基11)。发现GST 11 - 11的甲基化会抑制该同工酶对1 - 氯 - 2,4 - 二硝基苯的结合活性;结合活性的抑制程度与GST 11 - 11的甲基化程度相关。肾脏和肝脏中存在针对GST亚基3、4和11的GST-MT活性,在肺和心脏中可检测到,但在大脑和睾丸中不存在。对来自肝脏和肾脏的GST-MTs进行阴离子交换层析表明存在四种不同形式的GST-MT(I - IV),并表明GST-MT同工酶III和IV在肾脏中的浓度明显低于肝脏。本文表明甲基化是一种酶催化反应,对于不同的GST同工酶,其底物特异性不同,GST-MT在组织中存在表达依赖性,肝脏和肾脏中存在多种形式的该酶,并且甲基化会抑制GST活性。(摘要截短至400字)