Developmental aspects of a unique glutathione S-transferase subunit Yx in the liver cytosol from rats with hereditary hyperbilirubinuria. Comparison with rat fetal liver transferase subunit Yfetus
- PMID: 1567376
- PMCID: PMC1131029
- DOI: 10.1042/bj2830307
Developmental aspects of a unique glutathione S-transferase subunit Yx in the liver cytosol from rats with hereditary hyperbilirubinuria. Comparison with rat fetal liver transferase subunit Yfetus
Abstract
The unique glutathione S-transferase (GST) subunit Yx, which is undetectable in normal adult rat liver cytosol, was shown to occur in the liver cytosol of rats with hereditary hyperbilirubinuria (EHB). The Yx subunit is a member of the Alpha-class GST subunits, and is immunologically closely related to the Yc subunit. The Yx subunit has an apparent M(r) of 26,400, different from those of Ya (M(r) 25,800), Yb1 and Yb2 (both M(r) 27,200) and Yc (M(r) 28,400). During postnatal development in livers of EHB rats, the Yx subunit concentration in either sex was highest during the first week post partum and declined rapidly with age. Although the concentration of subunit Yx at 8 weeks of age accounted for about 60% in females and 40% in males of that observed in 1-week-old 'neonatal' male EHB rats, concentrations in females thereafter increased gradually to almost the neonatal level and remained at this high level at least up to 37 weeks of age, whereas the concentration in males did not increase again. Thus the post-pubertal Yx subunit concentration was 2-fold higher in females than in males. In contrast, in normal Sprague-Dawley rat liver, the Yfetus subunit, with the same M(r) as the Yx subunit, had the highest concentration in 10-day-old animals, declined rapidly thereafter, and was not detectable in the post-pubertal period. The Yfetus subunit was also immunoreactive with an antibody against GST YcYc. The analysis of GST subunits by reverse-phase h.p.l.c. revealed that the Yx subunit was eluted at a retention time different from other known subunits, but coincided with that of Yfetus. The N-terminal amino acid sequence of the Yx subunit displayed a high degree of sequence similarity to that of the Yfetus subunit. These data suggest that the Yx subunit in EHB rats may be very similar to, if not identical with, the Yfetus subunit.
Similar articles
-
A specific glutathione S-transferase isozyme occurring in hereditary hyperbilirubinuria rats.J Biochem. 1991 Jan;109(1):3-5. doi: 10.1093/oxfordjournals.jbchem.a123346. J Biochem. 1991. PMID: 2016270
-
Subunit Ya-specific glutathione peroxidase activity toward cholesterol 7-hydroperoxides of glutathione S-transferases in cytosols from rat liver and skin.J Biol Chem. 1997 Feb 21;272(8):4763-9. doi: 10.1074/jbc.272.8.4763. J Biol Chem. 1997. PMID: 9030530
-
Hepatic glutathione S-transferases in mice fed on a diet containing the anticarcinogenic antioxidant butylated hydroxyanisole. Isolation of mouse glutathione S-transferase heterodimers by gradient elution of the glutathione-Sepharose affinity matrix.Biochem J. 1991 Jul 15;277 ( Pt 2)(Pt 2):501-12. doi: 10.1042/bj2770501. Biochem J. 1991. PMID: 1859377 Free PMC article.
-
A new class of rat glutathione S-transferase Yrs-Yrs inactivating reactive sulfate esters as metabolites of carcinogenic arylmethanols.J Biol Chem. 1990 Jul 15;265(20):11973-81. J Biol Chem. 1990. PMID: 2114406
-
Regulation of mouse glutathione S-transferases by chemoprotectors. Molecular evidence for the existence of three distinct alpha-class glutathione S-transferase subunits, Ya1, Ya2, and Ya3, in mouse liver.Biochem J. 1991 Jun 1;276 ( Pt 2)(Pt 2):461-9. doi: 10.1042/bj2760461. Biochem J. 1991. PMID: 2049074 Free PMC article.
Cited by
-
Effects of hyperbilirubinaemia on glutathione S-transferase isoenzymes in cerebellar cortex of the Gunn rat.Biochem J. 1993 Apr 15;291 ( Pt 2)(Pt 2):453-61. doi: 10.1042/bj2910453. Biochem J. 1993. PMID: 8484726 Free PMC article.
-
Growth hormone- and testosterone-dependent regulation of glutathione transferase subunit A5 in rat liver.Biochem J. 1998 Jun 15;332 ( Pt 3)(Pt 3):763-8. doi: 10.1042/bj3320763. Biochem J. 1998. PMID: 9620880 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials