Tee L B, Gilmore K S, Meyer D J, Ketterer B, Vandenberghe Y, Yeoh G C
Department of Physiology, University of Western Australia, Nedlands.
Biochem J. 1992 Feb 15;282 ( Pt 1)(Pt 1):209-18. doi: 10.1042/bj2820209.
The ontogeny of rat liver glutathione S-transferase (EC 2.5.1.18) (GSTs) during foetal and postnatal development was investigated. The GSTs are dimers, the subunits of which belong to three multigene families, Alpha (subunits 1, 2, 8 and 10), Mu (subunits 3, 4, 6, 9 and 11) and Pi (subunit 7) [Mannervik, Alin, Guthenberg, Jennsson, Tahir, Warholm & Jörnvall (1985) Proc. Natl. Acad. Sci. U.S.A. 82, 7202-7206; Kispert, Meyer, Lalor, Coles & Ketterer (1989) Biochem. J. 260, 789-793]. There is considerable structural homology within each gene family, with the result that whereas reverse-phase h.p.l.c. successfully differentiates individual subunits, immunocytochemical and Northern-blotting analyses may only differentiate families. Enzymic activity, h.p.l.c. and Northern blotting indicated that expression of GST increased from very low levels at 12 days of foetal growth to substantial amounts at day 21. At birth, GST concentrations underwent a dramatic decline and remained low until 5-10 days post partum, after which they increased to adult levels. During the period under study, GST subunits underwent differential expression. The Mu family had a lower level of expression than the Alpha family, and, within the Alpha family, subunit 1 was more dominant in the adult than the foetus. Subunit 2 is the major form in the foetus. Most noteworthy were subunits 7 and 10, which were prominent in the foetus, but present at low levels post partum. Immunocytochemical analysis of the 17-day foetal and newborn rat livers showed marked differences in the distribution of GSTs in hepatocytes. In the 17-day foetal liver Pi greater than Alpha greater than Mu whereas in the newborns Alpha greater than Mu much greater than Pi. Erythropoietic cells were not stained for any of the three GST families. Steady-state mRNA concentrations in the foetus correlated with the relative transcription of the Alpha, Mu and Pi class genes. However, in those genes expressed post partum, namely the Alpha and Mu class, low transcriptional activity was associated with high concentrations of mRNA. This suggests that there is a switch from transcriptional control to post-transcriptional control at birth. GST 7-7 appears to be regulated predominantly by transcription throughout the period of liver development under observation.
研究了大鼠肝脏谷胱甘肽S-转移酶(EC 2.5.1.18)(GSTs)在胎儿期和出生后发育过程中的个体发生。GSTs是二聚体,其亚基属于三个多基因家族,即α家族(亚基1、2、8和10)、μ家族(亚基3、4、6、9和11)和π家族(亚基7)[Mannervik,Alin,Guthenberg,Jennsson,Tahir,Warholm和Jörnvall(1985年)《美国国家科学院院刊》82,7202 - 7206;Kispert,Meyer,Lalor,Coles和Ketterer(1989年)《生物化学杂志》260,789 - 793]。每个基因家族内存在相当大的结构同源性,结果是虽然反相高效液相色谱法能成功区分各个亚基,但免疫细胞化学和Northern印迹分析可能只能区分家族。酶活性、高效液相色谱法和Northern印迹表明,GST的表达从胎儿生长12天时的极低水平增加到21天时的大量表达。出生时,GST浓度急剧下降并在产后5 - 10天内保持较低水平,此后它们增加到成年水平。在研究期间,GST亚基经历了差异表达。μ家族的表达水平低于α家族,并且在α家族内,亚基1在成年大鼠中比在胎儿中更占优势。亚基2是胎儿中的主要形式。最值得注意的是亚基7和10,它们在胎儿中很突出,但在产后水平较低。对17天胎儿和新生大鼠肝脏的免疫细胞化学分析显示,GSTs在肝细胞中的分布存在明显差异。在17天胎儿肝脏中,π>α>μ,而在新生大鼠中,α>μ>>π。造血细胞对这三个GST家族中的任何一个都没有染色。胎儿中的稳态mRNA浓度与α、μ和π类基因的相对转录相关。然而,在产后表达的那些基因,即α和μ类基因中,低转录活性与高浓度的mRNA相关。这表明在出生时存在从转录控制到转录后控制的转变。在观察到的肝脏发育期间,GST 7 - 7似乎主要受转录调控。