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. 1993 Aug 15;294(Pt 1):173–180. doi: 10.1042/bj2940173

Species-specific induction of cytochrome P-450 4A RNAs: PCR cloning of partial guinea-pig, human and mouse CYP4A cDNAs.

D R Bell 1, N J Plant 1, C G Rider 1, L Na 1, S Brown 1, I Ateitalla 1, S K Acharya 1, M H Davies 1, E Elias 1, N A Jenkins 1, et al.
PMCID: PMC1134581  PMID: 8363569

Abstract

PCR was used to demonstrate the presence of a conserved region and to clone novel members of the cytochrome P-450 4A gene family from guinea pig, human and mouse cDNAs. This strategy is based on the sequences at nucleotides 925-959 and at the haem binding domain (nucleotides 1381-1410) of the rat CYP4A1 gene. Murine Cyp4a clones showed high sequence identity with members of the rat gene family, but CYP4A clones from human and guinea pig were equally similar to the rat/mouse genes, suggesting that the rat/mouse line had undergone gene duplication events after divergence from human and guinea-pig lines. The mouse Cyp4a-12 clone was localized to chromosome 4 using interspecific backcross mapping, in a region of synteny with human chromosome 1. The assignment of the human CYP4A11 gene to chromosome 1 was confirmed by somatic cell hybridization. An RNAase protection assay was shown to discriminate between the murine Cyp4a-10 and Cyp4a-12 cDNAs. Treatment of mice with the potent peroxisome proliferator methylclofenapate (25 mg/kg) induced Cyp4a-10 RNA in liver, and to a lesser extent in kidney; there was no sex difference in this response. Cyp4a-12 RNA was present at high levels in male control liver and kidney samples, and was not induced by treatment with methylclofenapate. However, Cyp4a-12 RNA was present at low levels in control female liver and kidney RNA, and was greatly induced in both organs by methylclofenapate. Guinea pigs were exposed to methylclofenapate (50 mg/kg), but there was no significant induction of the guinea-pig CYP4A13 RNA. These findings are consistent with a species difference in response to peroxisome proliferators between the rat/mouse and the guinea pig.

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  1. Bell D. R., Bars R. G., Elcombe C. R. Differential tissue-specific expression and induction of cytochrome P450IVA1 and acyl-CoA oxidase. Eur J Biochem. 1992 Jun 15;206(3):979–986. doi: 10.1111/j.1432-1033.1992.tb17009.x. [DOI] [PubMed] [Google Scholar]
  2. Bell D. R., Bars R. G., Gibson G. G., Elcombe C. R. Localization and differential induction of cytochrome P450IVA and acyl-CoA oxidase in rat liver. Biochem J. 1991 Apr 1;275(Pt 1):247–252. doi: 10.1042/bj2750247. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bell D. R., Elcombe C. R. Induction of acyl-CoA oxidase and cytochrome P450IVA1 RNA in rat primary hepatocyte culture by peroxisome proliferators. Biochem J. 1991 Nov 15;280(Pt 1):249–253. doi: 10.1042/bj2800249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bradfield J. Y., Lee Y. H., Keeley L. L. Cytochrome P450 family 4 in a cockroach: molecular cloning and regulation by regulation by hypertrehalosemic hormone. Proc Natl Acad Sci U S A. 1991 May 15;88(10):4558–4562. doi: 10.1073/pnas.88.10.4558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Brown S., Chalmers D. E. Microsomal epoxide hydrolase activity in human x mouse hybrid cells. Biochem Biophys Res Commun. 1986 Jun 13;137(2):775–780. doi: 10.1016/0006-291x(86)91146-0. [DOI] [PubMed] [Google Scholar]
  6. Brown S., Lalley P. A., Minna J. D. Assignment of the gene for peptidase S (PEPS) to chromosome 4 in man and confirmation of peptidase D (PEPD) assignment to chromosome 19. Cytogenet Cell Genet. 1978;22(1-6):167–171. doi: 10.1159/000130928. [DOI] [PubMed] [Google Scholar]
  7. Brown S., Wiebel F. J., Gelboin H. V., Minna J. D. Assignment of a locus required for flavoprotein-linked monooxygenase expression to human chromosome 2. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4628–4632. doi: 10.1073/pnas.73.12.4628. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cathala G., Savouret J. F., Mendez B., West B. L., Karin M., Martial J. A., Baxter J. D. A method for isolation of intact, translationally active ribonucleic acid. DNA. 1983;2(4):329–335. doi: 10.1089/dna.1983.2.329. [DOI] [PubMed] [Google Scholar]
  9. Ceci J. D., Siracusa L. D., Jenkins N. A., Copeland N. G. A molecular genetic linkage map of mouse chromosome 4 including the localization of several proto-oncogenes. Genomics. 1989 Nov;5(4):699–709. doi: 10.1016/0888-7543(89)90111-0. [DOI] [PubMed] [Google Scholar]
  10. Copeland N. G., Jenkins N. A. Development and applications of a molecular genetic linkage map of the mouse genome. Trends Genet. 1991 Apr;7(4):113–118. doi: 10.1016/0168-9525(91)90455-y. [DOI] [PubMed] [Google Scholar]
  11. Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dirven H. A., Peters J. G., Gibson G. G., Peters W. H., Jongeneelen F. J. Lauric acid hydroxylase activity and cytochrome P450 IV family proteins in human liver microsomes. Biochem Pharmacol. 1991 Oct 9;42(9):1841–1844. doi: 10.1016/0006-2952(91)90524-9. [DOI] [PubMed] [Google Scholar]
  13. Earnshaw D., Dale J. W., Goldfarb P. S., Gibson G. G. Differential splicing in the 3' non-coding region of rat cytochrome P-452 (P450 IVA1) mRNA. FEBS Lett. 1988 Aug 29;236(2):357–361. doi: 10.1016/0014-5793(88)80055-3. [DOI] [PubMed] [Google Scholar]
  14. Elcombe C. R., Mitchell A. M. Peroxisome proliferation due to di(2-ethylhexyl) phthalate (DEHP): species differences and possible mechanisms. Environ Health Perspect. 1986 Dec;70:211–219. doi: 10.1289/ehp.8670211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Elcombe C. R., Mitchell A. M. Peroxisome proliferation due to di(2-ethylhexyl) phthalate (DEHP): species differences and possible mechanisms. Environ Health Perspect. 1986 Dec;70:211–219. doi: 10.1289/ehp.8670211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Gasser R., Philpot R. M. Primary structures of cytochrome P-450 isozyme 5 from rabbit and rat and regulation of species-dependent expression and induction in lung and liver: identification of cytochrome P-450 gene subfamily IVB. Mol Pharmacol. 1989 May;35(5):617–625. [PubMed] [Google Scholar]
  17. Graur D., Hide W. A., Li W. H. Is the guinea-pig a rodent? Nature. 1991 Jun 20;351(6328):649–652. doi: 10.1038/351649a0. [DOI] [PubMed] [Google Scholar]
  18. Hanhijärvi H., Ylinen M., Kojo A., Kosma V. M. Elimination and toxicity of perfluorooctanoic acid during subchronic administration in the Wistar rat. Pharmacol Toxicol. 1987 Jul;61(1):66–68. doi: 10.1111/j.1600-0773.1987.tb01775.x. [DOI] [PubMed] [Google Scholar]
  19. Hardwick J. P., Song B. J., Huberman E., Gonzalez F. J. Isolation, complementary DNA sequence, and regulation of rat hepatic lauric acid omega-hydroxylase (cytochrome P-450LA omega). Identification of a new cytochrome P-450 gene family. J Biol Chem. 1987 Jan 15;262(2):801–810. [PubMed] [Google Scholar]
  20. Henderson C. J., Scott A. R., Yang C. S., Wolf C. R. Testosterone-mediated regulation of mouse renal cytochrome P-450 isoenzymes. Biochem J. 1990 Mar 15;266(3):675–681. doi: 10.1042/bj2660675. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Henderson C. J., Wolf C. R. Evidence that the androgen receptor mediates sexual differentiation of mouse renal cytochrome P450 expression. Biochem J. 1991 Sep 1;278(Pt 2):499–503. doi: 10.1042/bj2780499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Jenkins N. A., Copeland N. G., Taylor B. A., Lee B. K. Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus. J Virol. 1982 Jul;43(1):26–36. doi: 10.1128/jvi.43.1.26-36.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kimura S., Hardwick J. P., Kozak C. A., Gonzalez F. J. The rat clofibrate-inducible CYP4A subfamily. II. cDNA sequence of IVA3, mapping of the Cyp4a locus to mouse chromosome 4, and coordinate and tissue-specific regulation of the CYP4A genes. DNA. 1989 Sep;8(7):517–525. doi: 10.1089/dna.1.1989.8.517. [DOI] [PubMed] [Google Scholar]
  24. Lake B. G., Evans J. G., Gray T. J., Körösi S. A., North C. J. Comparative studies on nafenopin-induced hepatic peroxisome proliferation in the rat, Syrian hamster, guinea pig, and marmoset. Toxicol Appl Pharmacol. 1989 Jun 1;99(1):148–160. doi: 10.1016/0041-008x(89)90120-8. [DOI] [PubMed] [Google Scholar]
  25. Lock E. A., Mitchell A. M., Elcombe C. R. Biochemical mechanisms of induction of hepatic peroxisome proliferation. Annu Rev Pharmacol Toxicol. 1989;29:145–163. doi: 10.1146/annurev.pa.29.040189.001045. [DOI] [PubMed] [Google Scholar]
  26. Makowska J. M., Bonner F. W., Gibson G. G. Comparative induction of cytochrome P450IVA1 and peroxisome proliferation by ciprofibrate in the rat and marmoset. Arch Toxicol. 1991;65(2):106–113. doi: 10.1007/BF02034935. [DOI] [PubMed] [Google Scholar]
  27. Miles J. S., Moss J. E., Taylor B. A., Burchell B., Wolf C. R. Mapping genes encoding drug-metabolizing enzymes in recombinant inbred mice. Genomics. 1991 Oct;11(2):309–316. doi: 10.1016/0888-7543(91)90137-4. [DOI] [PubMed] [Google Scholar]
  28. Milton M. N., Elcombe C. R., Gibson G. G. On the mechanism of induction of microsomal cytochrome P450IVA1 and peroxisome proliferation in rat liver by clofibrate. Biochem Pharmacol. 1990 Dec 15;40(12):2727–2732. doi: 10.1016/0006-2952(90)90594-b. [DOI] [PubMed] [Google Scholar]
  29. Moody D. E., Reddy J. K. The hepatic effects of hypolipidemic drugs (clofibrate, nafenopin, tibric acid, and Wy-14,643) on hepatic peroxisomes and peroxisome-associated enzymes. Am J Pathol. 1978 Feb;90(2):435–446. [PMC free article] [PubMed] [Google Scholar]
  30. Myers R. M., Larin Z., Maniatis T. Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes. Science. 1985 Dec 13;230(4731):1242–1246. doi: 10.1126/science.4071043. [DOI] [PubMed] [Google Scholar]
  31. Nebert D. W., Nelson D. R., Coon M. J., Estabrook R. W., Feyereisen R., Fujii-Kuriyama Y., Gonzalez F. J., Guengerich F. P., Gunsalus I. C., Johnson E. F. The P450 superfamily: update on new sequences, gene mapping, and recommended nomenclature. DNA Cell Biol. 1991 Jan-Feb;10(1):1–14. doi: 10.1089/dna.1991.10.1. [DOI] [PubMed] [Google Scholar]
  32. Nhamburo P. T., Gonzalez F. J., McBride O. W., Gelboin H. V., Kimura S. Identification of a new P450 expressed in human lung: complete cDNA sequence, cDNA-directed expression, and chromosome mapping. Biochemistry. 1989 Oct 3;28(20):8060–8066. doi: 10.1021/bi00446a014. [DOI] [PubMed] [Google Scholar]
  33. Orton T. C., Parker G. L. The effect of hypolipidemic agents on the hepatic microsomal drug-metabolizing enzyme system of the rat. Induction of cytochrome(s) P-450 with specificity toward terminal hydroxylation of lauric acid. Drug Metab Dispos. 1982 Mar-Apr;10(2):110–115. [PubMed] [Google Scholar]
  34. Paine A. J. The cytochrome P450 gene superfamily. Int J Exp Pathol. 1991 Jun;72(3):349–363. [PMC free article] [PubMed] [Google Scholar]
  35. Reddy J. K., Lalwani N. D., Qureshi S. A., Reddy M. K., Moehle C. M. Induction of hepatic peroxisome proliferation in nonrodent species, including primates. Am J Pathol. 1984 Jan;114(1):171–183. [PMC free article] [PubMed] [Google Scholar]
  36. Sanglard D., Loper J. C. Characterization of the alkane-inducible cytochrome P450 (P450alk) gene from the yeast Candida tropicalis: identification of a new P450 gene family. Gene. 1989 Mar 15;76(1):121–136. doi: 10.1016/0378-1119(89)90014-0. [DOI] [PubMed] [Google Scholar]
  37. Sharma R., Lake B. G., Foster J., Gibson G. G. Microsomal cytochrome P-452 induction and peroxisome proliferation by hypolipidaemic agents in rat liver. A mechanistic inter-relationship. Biochem Pharmacol. 1988 Apr 1;37(7):1193–1201. doi: 10.1016/0006-2952(88)90770-8. [DOI] [PubMed] [Google Scholar]
  38. Sohlenius A. K., Andersson K., DePierre J. W. The effects of perfluoro-octanoic acid on hepatic peroxisome proliferation and related parameters show no sex-related differences in mice. Biochem J. 1992 Aug 1;285(Pt 3):779–783. doi: 10.1042/bj2850779. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Strömstedt M., Hayashi S., Zaphiropoulos P. G., Gustafsson J. A. Cloning and characterization of a novel member of the cytochrome P450 subfamily IVA in rat prostate. DNA Cell Biol. 1990 Oct;9(8):569–577. doi: 10.1089/dna.1990.9.569. [DOI] [PubMed] [Google Scholar]
  40. Sundseth S. S., Waxman D. J. Sex-dependent expression and clofibrate inducibility of cytochrome P450 4A fatty acid omega-hydroxylases. Male specificity of liver and kidney CYP4A2 mRNA and tissue-specific regulation by growth hormone and testosterone. J Biol Chem. 1992 Feb 25;267(6):3915–3921. [PubMed] [Google Scholar]
  41. Tamburini P. P., Masson H. A., Bains S. K., Makowski R. J., Morris B., Gibson G. G. Multiple forms of hepatic cytochrome P-450. Purification, characterisation and comparison of a novel clofibrate-induced isozyme with other major forms of cytochrome P-450. Eur J Biochem. 1984 Mar 1;139(2):235–246. doi: 10.1111/j.1432-1033.1984.tb07999.x. [DOI] [PubMed] [Google Scholar]

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