Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1994 May 1;299(Pt 3):711–717. doi: 10.1042/bj2990711

Immunological analysis of developmental changes in ecdysone 20-mono-oxygenase expression in the cotton leafworm, Spodoptera littoralis.

J H Chen 1, T Hara 1, M J Fisher 1, H H Rees 1
PMCID: PMC1138078  PMID: 8192659

Abstract

The developmental changes in ecdysone 20-mono-oxygenase during the sixth larval instar of the cotton leafworm, Spodoptera littoralis, were investigated. The specific activity of mitochondrial ecdysone 20-mono-oxygenase in the fat-body exhibited a distinct peak at 72 h, at which time the larvae stop feeding. Immunoblot analyses, using antibodies raised against components of vertebrate mitochondrial steroidogenic enzyme systems [anti-(cytochrome P-450scc), anti-(cytochrome P-450(11) beta), anti-adrenodoxin and anti-(adrenodoxin reductase) antibodies], revealed the presence of specific immunoreactive polypeptides in fat-body mitochondrial extracts. In addition, these antibodies effectively inhibited fat-body mitochondrial ecdysone 20-mono-oxygenase activity. This suggests that the S. littoralis steroid-hydroxylating system(s) may contain polypeptide components analogous to those present in vertebrates. A close correlation between developmental changes in mitochondrial ecdysone 20-mono-oxygenase activity and the abundance of polypeptides (approx. 66 kDa and 50 kDa) recognized by the anti-(cytochrome P-450(11) beta) antibody and a polypeptide (approx. 52 kDa) recognized by the anti-(adrenodoxin reductase) antibody were observed in both fat-body and midgut. These results suggest that developmental changes in the abundance of components of the ecdysone 20-mono-oxygenase system may play an important role in the developmental regulation of the enzyme expression and, hence, of 20-hydroxyecdysone titre.

Full text

PDF
713

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Addya S., Zheng Y. M., Shayiq R. M., Fan J. Y., Avadhani N. G. Characterization of a female-specific hepatic mitochondrial cytochrome P-450 whose steady-state level is modulated by testosterone. Biochemistry. 1991 Aug 27;30(34):8323–8330. doi: 10.1021/bi00098a007. [DOI] [PubMed] [Google Scholar]
  2. Aflalo L., Meidan R. The hormonal regulation of cholesterol side-chain cleavage cytochrome P450, adrenodoxin, and their messenger ribonucleic acid expression in bovine small-like and large-like luteal cells: relationship with progesterone production. Endocrinology. 1993 Jan;132(1):410–416. doi: 10.1210/endo.132.1.8380385. [DOI] [PubMed] [Google Scholar]
  3. 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]
  4. Coon M. J., Ding X. X., Pernecky S. J., Vaz A. D. Cytochrome P450: progress and predictions. FASEB J. 1992 Jan 6;6(2):669–673. doi: 10.1096/fasebj.6.2.1537454. [DOI] [PubMed] [Google Scholar]
  5. Feyereisen R., Durst F. Development of microsomal cytochrome P-450 monooxygenases during the last larval instar of the locust, Locusta migratoria: correlation with the hemolymph 20-hydroxyecdysone titer. Mol Cell Endocrinol. 1980 Nov;20(2):157–169. doi: 10.1016/0303-7207(80)90079-9. [DOI] [PubMed] [Google Scholar]
  6. Feyereisen R., Koener J. F., Farnsworth D. E., Nebert D. W. Isolation and sequence of cDNA encoding a cytochrome P-450 from an insecticide-resistant strain of the house fly, Musca domestica. Proc Natl Acad Sci U S A. 1989 Mar;86(5):1465–1469. doi: 10.1073/pnas.86.5.1465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gandhi R., Varak E., Goldberg M. L. Molecular analysis of a cytochrome P450 gene of family 4 on the Drosophila X chromosome. DNA Cell Biol. 1992 Jun;11(5):397–404. doi: 10.1089/dna.1992.11.397. [DOI] [PubMed] [Google Scholar]
  8. Hara T., Kimura T. Active complex between adrenodoxin reductase and adrenodoxin in the cytochrome P-450scc reduction reaction. J Biochem. 1989 Apr;105(4):601–605. doi: 10.1093/oxfordjournals.jbchem.a122711. [DOI] [PubMed] [Google Scholar]
  9. Hara T., Kimura T. Purification and catalytic properties of a cross-linked complex between adrenodoxin reductase and adrenodoxin. J Biochem. 1989 Apr;105(4):594–600. doi: 10.1093/oxfordjournals.jbchem.a122710. [DOI] [PubMed] [Google Scholar]
  10. Imaoka S., Fujita S., Funae Y. Age-dependent expression of cytochrome P-450s in rat liver. Biochim Biophys Acta. 1991 Oct 21;1097(3):187–192. doi: 10.1016/0925-4439(91)90034-7. [DOI] [PubMed] [Google Scholar]
  11. John M. E., John M. C., Simpson E. R., Waterman M. R. Regulation of cytochrome P-45011 beta gene expression by adrenocorticotropin. J Biol Chem. 1985 May 10;260(9):5760–5767. [PubMed] [Google Scholar]
  12. Johnson P., Rees H. H. The mechanism of C-20 hydroxylation of alpha-ecdysone in the desert locust, Schistocerca gregaria. Biochem J. 1977 Dec 15;168(3):513–520. doi: 10.1042/bj1680513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Katagiri M., Takemori S., Itagaki E., Suhara K. Purification of adrenal cytochrome P-450 (cholesterol desmolase and steroid 11beta- and 18-hydroxylase). Methods Enzymol. 1978;52:124–132. doi: 10.1016/s0076-6879(78)52014-4. [DOI] [PubMed] [Google Scholar]
  14. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  15. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  16. Miller W. L. Molecular biology of steroid hormone synthesis. Endocr Rev. 1988 Aug;9(3):295–318. doi: 10.1210/edrv-9-3-295. [DOI] [PubMed] [Google Scholar]
  17. Mitchell M. J., Smith S. L. Ecdysone 20-monooxygenase activity throughout the life cycle of Drosophila melanogaster. Gen Comp Endocrinol. 1988 Dec;72(3):467–470. doi: 10.1016/0016-6480(88)90170-0. [DOI] [PubMed] [Google Scholar]
  18. Nelson D. R., Kamataki T., Waxman D. J., Guengerich F. P., Estabrook R. W., Feyereisen R., Gonzalez F. J., Coon M. J., Gunsalus I. C., Gotoh O. The P450 superfamily: update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature. DNA Cell Biol. 1993 Jan-Feb;12(1):1–51. doi: 10.1089/dna.1993.12.1. [DOI] [PubMed] [Google Scholar]
  19. Nigg H. N., Svoboda J. A., Thompson M. J., Dutky S. R., Kaplanis J. N., Robbins W. E. Ecdysome 20-hydroxylase from the midgut of the tobacco hornworm (Manduca sexta L.). Experientia. 1976 Apr 15;32(4):438–439. doi: 10.1007/BF01920781. [DOI] [PubMed] [Google Scholar]
  20. Scott J. G., Lee S. S. Tissue distribution of microsomal cytochrome P-450 monooxygenases and their inducibility by phenobarbital in the insecticide resistant LPR strain of house fly, Musca domestica L. Insect Biochem Mol Biol. 1993 Sep;23(6):729–738. doi: 10.1016/0965-1748(93)90047-v. [DOI] [PubMed] [Google Scholar]
  21. Smith S. L., Bollenbacher W. E., Gilbert L. I. Ecdysone 20-monooxygenase activity during larval-pupal development of Manduca sexta. Mol Cell Endocrinol. 1983 Aug;31(2-3):227–251. doi: 10.1016/0303-7207(83)90151-x. [DOI] [PubMed] [Google Scholar]
  22. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Watabe S., Hara T., Kohno H., Hiroi T., Yago N., Nakazawa T. In vitro degradation of mitochondrial proteins by ATP-dependent protease in bovine adrenal cortex. J Biochem. 1993 Jun;113(6):672–676. doi: 10.1093/oxfordjournals.jbchem.a124101. [DOI] [PubMed] [Google Scholar]
  24. Waters L. C., Zelhof A. C., Shaw B. J., Ch'ang L. Y. Possible involvement of the long terminal repeat of transposable element 17.6 in regulating expression of an insecticide resistance-associated P450 gene in Drosophila. Proc Natl Acad Sci U S A. 1992 Jun 1;89(11):4855–4859. doi: 10.1073/pnas.89.11.4855. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES