Large deletion of androsterone UDP-glucuronosyltransferase gene in the inherited deficient strain of Wistar rats
- PMID: 1737068
- DOI: 10.1016/0925-4439(92)90148-g
Large deletion of androsterone UDP-glucuronosyltransferase gene in the inherited deficient strain of Wistar rats
Abstract
LA Wistar rats have a deficiency of androsterone UDP-glucuronosyltransferase (UDPGT) and are present in Wistar rat colonies around the world. In order to clarify the molecular mechanism of the deficiency, androsterone UDPGT cDNA clone, pGT2 was isolated from rat liver cDNA library and was digested with restriction enzymes to afford three probes for Northern and Southern blot analyses in HA (normal), heterozygous LA and LA Wistar rats. In Northern blot analysis, androsterone UDPGT mRNA was totally absent in LA Wistar rat liver. Southern blot analysis suggested a large deletion of androsterone UDPGT gene in the rats. Genomic DNA amplifications with synthetic primers which have nucleotide sequences corresponding to the 5'-region of androsterone UDPGT cDNA, suggested that androsterone UDPGT gene has exon 1 with a length of some 700 bp and that this exon is deleted in LA Wistar rats. Based on these lines of evidence, it is concluded that the large portion of androsterone UDPGT gene is deleted in LA Wistar rats, which results in the absence of androsterone UDPGT mRNA and consequently the corresponding enzyme protein.
Similar articles
-
The full length coding sequence of rat liver androsterone UDP-glucuronyltransferase cDNA and comparison with other members of this gene family.Nucleic Acids Res. 1986 Jan 24;14(2):779-95. doi: 10.1093/nar/14.2.779. Nucleic Acids Res. 1986. PMID: 3003696 Free PMC article.
-
The 3-methylcholanthrene-inducible UDP-glucuronosyltransferase deficiency in the hyperbilirubinemic rat (Gunn rat) is caused by a -1 frameshift mutation.J Biol Chem. 1989 Dec 15;264(35):21302-7. J Biol Chem. 1989. PMID: 2512292
-
The molecular basis of the inherited deficiency of androsterone UDP-glucuronyltransferase in Wistar rats.FEBS Lett. 1987 Mar 23;213(2):448-52. doi: 10.1016/0014-5793(87)81540-5. FEBS Lett. 1987. PMID: 2881811
-
Molecular basis of multiple UDP-glucuronosyltransferase isoenzyme deficiencies in the hyperbilirubinemic rat (Gunn rat).J Biol Chem. 1991 Dec 15;266(35):24048-52. J Biol Chem. 1991. PMID: 1748678
-
[Genetic defect of the hyperbilirubinemic Gunn rat, a model for Crigler-Najjar syndrome type I].Nihon Rinsho. 1993 Feb;51(2):501-6. Nihon Rinsho. 1993. PMID: 8096554 Review. Japanese.
Cited by
-
Effects of thyroid status and thyrostatic drugs on hepatic glucuronidation of lodothyronines and other substrates in rats : Induction of phenol UDP-glucuronyltransferase by methimazole.Endocrine. 1996 Feb;4(1):79-85. doi: 10.1007/BF02738878. Endocrine. 1996. PMID: 21153295
-
Role of UDP-glucuronosyltransferase (UGT) 2B2 in metabolism of triiodothyronine: effect of microsomal enzyme inducers in Sprague Dawley and UGT2B2-deficient Fischer 344 rats.Toxicol Sci. 2010 Aug;116(2):413-21. doi: 10.1093/toxsci/kfq125. Epub 2010 Apr 26. Toxicol Sci. 2010. PMID: 20421340 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources