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. 1991 Apr;11(4):1846–1853. doi: 10.1128/mcb.11.4.1846

Ecdysterone regulatory elements function as both transcriptional activators and repressors.

L Dobens 1, K Rudolph 1, E M Berger 1
PMCID: PMC359858  PMID: 2005885

Abstract

A synthetic, 23-bp ecdysterone regulatory element (EcRE), derived from the upstream region of the Drosophila melanogaster hsp27 gene, was inserted adjacent to the herpes simplex virus thymidine kinase promoter fused to a bacterial gene for chloramphenicol acetyltransferase (CAT). Hybrid constructs were transfected into Drosophila S3 cells and assayed for ecdysterone-inducible CAT expression. In the absence of ecdysterone a tandem pair of EcREs repressed the high constitutive level of CAT activity found after transfection with the parent reporter plasmid alone. After hormone addition very high levels of CAT activity were observed. Insertion of the EcRE pair 3' of the CAT gene also led to high levels of ecdysterone-induced CAT expression, but the repression of high constitutive levels of CAT activity failed to occur. The EcRE-CAT construct was cotransfected with plasmids containing tandem 10-mers or 40-mers of the EcRE but lacking a reporter gene. These additional EcREs led to a reduced level of ecdysterone-induced CAT activity and to an elevation of basal CAT activity in the absence of hormone. The data suggest that the receptor binds to the EcRE in the absence of hormone, blocking basal transcription from a constitutive promoter. In the presence of ecdysterone, receptor-hormone binding to the EcRE leads to greatly enhanced transcription.

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Selected References

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  1. Amin J., Ananthan J., Voellmy R. Key features of heat shock regulatory elements. Mol Cell Biol. 1988 Sep;8(9):3761–3769. doi: 10.1128/mcb.8.9.3761. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ashburner M., Bonner J. J. The induction of gene activity in drosophilia by heat shock. Cell. 1979 Jun;17(2):241–254. doi: 10.1016/0092-8674(79)90150-8. [DOI] [PubMed] [Google Scholar]
  3. Ayme A., Tissières A. Locus 67B of Drosophila melanogaster contains seven, not four, closely related heat shock genes. EMBO J. 1985 Nov;4(11):2949–2954. doi: 10.1002/j.1460-2075.1985.tb04028.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cheney C. M., Shearn A. Developmental regulation of Drosophila imaginal disc proteins: synthesis of a heat shock protein under non-heat-shock conditions. Dev Biol. 1983 Feb;95(2):325–330. doi: 10.1016/0012-1606(83)90033-7. [DOI] [PubMed] [Google Scholar]
  5. Cherbas P., Cherbas L., Williams C. M. Induction of acetylcholinesterase activity by beta-ecdysone in a Drosophila cell line. Science. 1977 Jul 15;197(4300):275–277. doi: 10.1126/science.877552. [DOI] [PubMed] [Google Scholar]
  6. Cohen R. S., Meselson M. Separate regulatory elements for the heat-inducible and ovarian expression of the Drosophila hsp26 gene. Cell. 1985 Dec;43(3 Pt 2):737–746. doi: 10.1016/0092-8674(85)90247-8. [DOI] [PubMed] [Google Scholar]
  7. Corces V., Holmgren R., Freund R., Morimoto R., Meselson M. Four heat shock proteins of Drosophila melanogaster coded within a 12-kilobase region in chromosome subdivision 67B. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5390–5393. doi: 10.1073/pnas.77.9.5390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Craig E. A., McCarthy B. J. Four Drosophila heat shock genes at 67B: characterization of recombinant plasmids. Nucleic Acids Res. 1980 Oct 10;8(19):4441–4457. doi: 10.1093/nar/8.19.4441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Dalman F. C., Koenig R. J., Perdew G. H., Massa E., Pratt W. B. In contrast to the glucocorticoid receptor, the thyroid hormone receptor is translated in the DNA binding state and is not associated with hsp90. J Biol Chem. 1990 Mar 5;265(7):3615–3618. [PubMed] [Google Scholar]
  10. Damm K., Thompson C. C., Evans R. M. Protein encoded by v-erbA functions as a thyroid-hormone receptor antagonist. Nature. 1989 Jun 22;339(6226):593–597. doi: 10.1038/339593a0. [DOI] [PubMed] [Google Scholar]
  11. Di Nocera P. P., Dawid I. B. Transient expression of genes introduced into cultured cells of Drosophila. Proc Natl Acad Sci U S A. 1983 Dec;80(23):7095–7098. doi: 10.1073/pnas.80.23.7095. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dudler R., Travers A. A. Upstream elements necessary for optimal function of the hsp 70 promoter in transformed flies. Cell. 1984 Sep;38(2):391–398. doi: 10.1016/0092-8674(84)90494-x. [DOI] [PubMed] [Google Scholar]
  13. Evans R. M. The steroid and thyroid hormone receptor superfamily. Science. 1988 May 13;240(4854):889–895. doi: 10.1126/science.3283939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Glaser R. L., Lis J. T. Multiple, compensatory regulatory elements specify spermatocyte-specific expression of the Drosophila melanogaster hsp26 gene. Mol Cell Biol. 1990 Jan;10(1):131–137. doi: 10.1128/mcb.10.1.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Glaser R. L., Wolfner M. F., Lis J. T. Spatial and temporal pattern of hsp26 expression during normal development. EMBO J. 1986 Apr;5(4):747–754. doi: 10.1002/j.1460-2075.1986.tb04277.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Gorman C. M., Moffat L. F., Howard B. H. Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells. Mol Cell Biol. 1982 Sep;2(9):1044–1051. doi: 10.1128/mcb.2.9.1044. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hoffman E. P., Corces V. G. Correct temperature induction and developmental regulation of a cloned heat shock gene transformed into the Drosophila germ line. Mol Cell Biol. 1984 Dec;4(12):2883–2889. doi: 10.1128/mcb.4.12.2883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Hoffman E., Corces V. Sequences involved in temperature and ecdysterone-induced transcription are located in separate regions of a Drosophila melanogaster heat shock gene. Mol Cell Biol. 1986 Feb;6(2):663–673. doi: 10.1128/mcb.6.2.663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Ireland R. C., Berger E. M. Synthesis of low molecular weight heat shock peptides stimulated by ecdysterone in a cultured Drosophila cell line. Proc Natl Acad Sci U S A. 1982 Feb;79(3):855–859. doi: 10.1073/pnas.79.3.855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Ireland R. C., Berger E., Sirotkin K., Yund M. A., Osterbur D., Fristrom J. Ecdysterone induces the transcription of four heat-shock genes in Drosophila S3 cells and imaginal discs. Dev Biol. 1982 Oct;93(2):498–507. doi: 10.1016/0012-1606(82)90137-3. [DOI] [PubMed] [Google Scholar]
  21. Klemenz R., Gehring W. J. Sequence requirement for expression of the Drosophila melanogaster heat shock protein hsp22 gene during heat shock and normal development. Mol Cell Biol. 1986 Jun;6(6):2011–2019. doi: 10.1128/mcb.6.6.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Koenig R. J., Lazar M. A., Hodin R. A., Brent G. A., Larsen P. R., Chin W. W., Moore D. D. Inhibition of thyroid hormone action by a non-hormone binding c-erbA protein generated by alternative mRNA splicing. Nature. 1989 Feb 16;337(6208):659–661. doi: 10.1038/337659a0. [DOI] [PubMed] [Google Scholar]
  23. Landon T. M., Sage B. A., Seeler B. J., O'Connor J. D. Characterization and partial purification of the Drosophila Kc cell ecdysteroid receptor. J Biol Chem. 1988 Apr 5;263(10):4693–4697. [PubMed] [Google Scholar]
  24. Lavin T. N., Baxter J. D., Horita S. The thyroid hormone receptor binds to multiple domains of the rat growth hormone 5'-flanking sequence. J Biol Chem. 1988 Jul 5;263(19):9418–9426. [PubMed] [Google Scholar]
  25. Lawson R., Mestril R., Luo Y., Voellmy R. Ecdysterone selectively stimulates the expression of a 23000-Da heat-shock protein-beta-galactosidase hybrid gene in cultured Drosophila cells. Dev Biol. 1985 Aug;110(2):321–330. doi: 10.1016/0012-1606(85)90091-0. [DOI] [PubMed] [Google Scholar]
  26. Levine M., Manley J. L. Transcriptional repression of eukaryotic promoters. Cell. 1989 Nov 3;59(3):405–408. doi: 10.1016/0092-8674(89)90024-x. [DOI] [PubMed] [Google Scholar]
  27. Mestril R., Rungger D., Schiller P., Voellmy R. Identification of a sequence element in the promoter of the Drosophila melanogaster hsp23 gene that is required for its heat activation. EMBO J. 1985 Nov;4(11):2971–2976. doi: 10.1002/j.1460-2075.1985.tb04031.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Mestril R., Schiller P., Amin J., Klapper H., Ananthan J., Voellmy R. Heat shock and ecdysterone activation of the Drosophila melanogaster hsp23 gene; a sequence element implied in developmental regulation. EMBO J. 1986 Jul;5(7):1667–1673. doi: 10.1002/j.1460-2075.1986.tb04410.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Morganelli C. M., Berger E. M., Pelham H. R. Transcription of Drosophila small hsp-tk hybrid genes is induced by heat shock and by ecdysterone in transfected Drosophila cells. Proc Natl Acad Sci U S A. 1985 Sep;82(17):5865–5869. doi: 10.1073/pnas.82.17.5865. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Morganelli C. M., Berger E. M. Transient expression of homologous genes in Drosophila cells. Science. 1984 Jun 1;224(4652):1004–1006. doi: 10.1126/science.224.4652.1004. [DOI] [PubMed] [Google Scholar]
  31. Nieto-Sotelo J., Wiederrecht G., Okuda A., Parker C. S. The yeast heat shock transcription factor contains a transcriptional activation domain whose activity is repressed under nonshock conditions. Cell. 1990 Aug 24;62(4):807–817. doi: 10.1016/0092-8674(90)90124-w. [DOI] [PubMed] [Google Scholar]
  32. Nordeen S. K. Luciferase reporter gene vectors for analysis of promoters and enhancers. Biotechniques. 1988 May;6(5):454–458. [PubMed] [Google Scholar]
  33. Pauli D., Tonka C. H. A Drosophila heat shock gene from locus 67B is expressed during embryogenesis and pupation. J Mol Biol. 1987 Nov 20;198(2):235–240. doi: 10.1016/0022-2836(87)90309-3. [DOI] [PubMed] [Google Scholar]
  34. Pauli D., Tonka C. H., Ayme-Southgate A. An unusual split Drosophila heat shock gene expressed during embryogenesis, pupation and in testis. J Mol Biol. 1988 Mar 5;200(1):47–53. doi: 10.1016/0022-2836(88)90332-4. [DOI] [PubMed] [Google Scholar]
  35. Pelham H. R. A regulatory upstream promoter element in the Drosophila hsp 70 heat-shock gene. Cell. 1982 Sep;30(2):517–528. doi: 10.1016/0092-8674(82)90249-5. [DOI] [PubMed] [Google Scholar]
  36. Perisic O., Xiao H., Lis J. T. Stable binding of Drosophila heat shock factor to head-to-head and tail-to-tail repeats of a conserved 5 bp recognition unit. Cell. 1989 Dec 1;59(5):797–806. doi: 10.1016/0092-8674(89)90603-x. [DOI] [PubMed] [Google Scholar]
  37. Riddihough G., Pelham H. R. Activation of the Drosophila hsp27 promoter by heat shock and by ecdysone involves independent and remote regulatory sequences. EMBO J. 1986 Jul;5(7):1653–1658. doi: 10.1002/j.1460-2075.1986.tb04408.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Riddihough G., Pelham H. R. An ecdysone response element in the Drosophila hsp27 promoter. EMBO J. 1987 Dec 1;6(12):3729–3734. doi: 10.1002/j.1460-2075.1987.tb02707.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Rusconi S., Yamamoto K. R. Functional dissection of the hormone and DNA binding activities of the glucocorticoid receptor. EMBO J. 1987 May;6(5):1309–1315. doi: 10.1002/j.1460-2075.1987.tb02369.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Schauer M., Chalepakis G., Willmann T., Beato M. Binding of hormone accelerates the kinetics of glucocorticoid and progesterone receptor binding to DNA. Proc Natl Acad Sci U S A. 1989 Feb;86(4):1123–1127. doi: 10.1073/pnas.86.4.1123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Schmid W., Strähle U., Schütz G., Schmitt J., Stunnenberg H. Glucocorticoid receptor binds cooperatively to adjacent recognition sites. EMBO J. 1989 Aug;8(8):2257–2263. doi: 10.1002/j.1460-2075.1989.tb08350.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Shuey D. J., Parker C. S. Binding of Drosophila heat-shock gene transcription factor to the hsp 70 promoter. Evidence for symmetric and dynamic interactions. J Biol Chem. 1986 Jun 15;261(17):7934–7940. [PubMed] [Google Scholar]
  43. Simon J. A., Lis J. T. A germline transformation analysis reveals flexibility in the organization of heat shock consensus elements. Nucleic Acids Res. 1987 Apr 10;15(7):2971–2988. doi: 10.1093/nar/15.7.2971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Sirotkin K., Davidson N. Developmentally regulated transcription from Drosophila melanogaster chromosomal site 67B. Dev Biol. 1982 Jan;89(1):196–210. doi: 10.1016/0012-1606(82)90307-4. [DOI] [PubMed] [Google Scholar]
  45. Sorger P. K., Nelson H. C. Trimerization of a yeast transcriptional activator via a coiled-coil motif. Cell. 1989 Dec 1;59(5):807–813. doi: 10.1016/0092-8674(89)90604-1. [DOI] [PubMed] [Google Scholar]
  46. Sorger P. K. Yeast heat shock factor contains separable transient and sustained response transcriptional activators. Cell. 1990 Aug 24;62(4):793–805. doi: 10.1016/0092-8674(90)90123-v. [DOI] [PubMed] [Google Scholar]
  47. Strähle U., Münsterberg A., Mestril R., Klock G., Ankenbauer W., Schmid W., Schütz G. Cooperative action of the glucocorticoid receptor and transcription factors. Cold Spring Harb Symp Quant Biol. 1988;53(Pt 2):835–841. doi: 10.1101/sqb.1988.053.01.095. [DOI] [PubMed] [Google Scholar]
  48. Tissières A., Mitchell H. K., Tracy U. M. Protein synthesis in salivary glands of Drosophila melanogaster: relation to chromosome puffs. J Mol Biol. 1974 Apr 15;84(3):389–398. doi: 10.1016/0022-2836(74)90447-1. [DOI] [PubMed] [Google Scholar]
  49. Topol J., Ruden D. M., Parker C. S. Sequences required for in vitro transcriptional activation of a Drosophila hsp 70 gene. Cell. 1985 Sep;42(2):527–537. doi: 10.1016/0092-8674(85)90110-2. [DOI] [PubMed] [Google Scholar]
  50. Veal J. M., Rill R. L. Sequence specificity of DNA cleavage by bis(1,10-phenanthroline)copper(I): effects of single base pair transitions on the cleavage of preferred pyrimidine-purine-pyrimidine triplets. Biochemistry. 1989 Apr 18;28(8):3243–3250. doi: 10.1021/bi00434a019. [DOI] [PubMed] [Google Scholar]
  51. Vitek M. P., Berger E. M. Steroid and high-temperature induction of the small heat-shock protein genes in Drosophila. J Mol Biol. 1984 Sep 15;178(2):173–189. doi: 10.1016/0022-2836(84)90138-4. [DOI] [PubMed] [Google Scholar]
  52. Voellmy R., Goldschmidt-Clermont M., Southgate R., Tissières A., Levis R., Gehring W. A DNA segment isolated from chromosomal site 67B in D. melanogaster contains four closely linked heat-shock genes. Cell. 1981 Jan;23(1):261–270. doi: 10.1016/0092-8674(81)90290-7. [DOI] [PubMed] [Google Scholar]
  53. Wiederrecht G., Shuey D. J., Kibbe W. A., Parker C. S. The Saccharomyces and Drosophila heat shock transcription factors are identical in size and DNA binding properties. Cell. 1987 Feb 13;48(3):507–515. doi: 10.1016/0092-8674(87)90201-7. [DOI] [PubMed] [Google Scholar]
  54. Willmann T., Beato M. Steroid-free glucocorticoid receptor binds specifically to mouse mammary tumour virus DNA. Nature. 1986 Dec 18;324(6098):688–691. doi: 10.1038/324688a0. [DOI] [PubMed] [Google Scholar]
  55. Xiao H., Lis J. T. A consensus sequence polymer inhibits in vivo expression of heat shock genes. Mol Cell Biol. 1986 Sep;6(9):3200–3206. doi: 10.1128/mcb.6.9.3200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Xiao H., Lis J. T. Germline transformation used to define key features of heat-shock response elements. Science. 1988 Mar 4;239(4844):1139–1142. doi: 10.1126/science.3125608. [DOI] [PubMed] [Google Scholar]
  57. Yund M. A., King D. S., Fristrom J. W. Ecdysteroid receptors in imaginal discs of Drosophila melanogaster. Proc Natl Acad Sci U S A. 1978 Dec;75(12):6039–6043. doi: 10.1073/pnas.75.12.6039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Zimmerman J. L., Petri W., Meselson M. Accumulation of a specific subset of D. melanogaster heat shock mRNAs in normal development without heat shock. Cell. 1983 Apr;32(4):1161–1170. doi: 10.1016/0092-8674(83)90299-4. [DOI] [PubMed] [Google Scholar]

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