Home LiteratureArticle Details
PMID: 2974921 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Concentration dependence of transcriptional transactivation in inducible E1A-containing human cells.

Molecular and cellular biology ·Vol. 8 ·No. 11 ·1988-11-00 ·Pages 4799-807

Brunet LJ, Berk AJ

Abstract

The adenovirus E1A proteins are essential for the normal temporal activation of transcription from every other adenoviral early promoter. High-level E1A expression in the absence of viral infection would facilitate biochemical studies of E1A-mediated transactivation. Toward this end, we introduced the adenovirus type 2 E1A gene under the control of the murine mammary tumor virus promoter into HeLa cells. Uninduced cells expressed little or no detectable E1A mRNA. Upon induction, mRNA levels accumulated to about 50% of the level observed in 293 cells. The level of E1A expression in these cells could be controlled by varying the concentration of the inducing glucocorticoid. Under these conditions of varying E1A concentrations, it was observed that activation of the E2, E3, and E4 promoters of H5dl312 initiated at the same E1A concentration and that transcription from each promoter increased as the E1A concentration increased. These results indicate that E1A-mediated transactivation is proportional to the concentration of E1A protein. E1A-dependent transcriptional stimulation of the E4 promoter was reproduced in an in vitro transcription system, demonstrating that expression of only the E1A proteins was sufficient to increase the transcriptional activity of nuclear extracts.

MeSH Terms
Adenovirus Early Proteins Cell Nucleus/metabolism Gene Expression Regulation HeLa Cells/metabolism Humans Oncogene Proteins, Viral/genetics,metabolism Promoter Regions, Genetic RNA, Messenger/genetics,metabolism Transcription, Genetic
Chemicals
Adenovirus Early Proteins Oncogene Proteins, Viral RNA, Messenger
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Brunet L J
Department of Microbiology, University of California, Los Angeles 90024.
Berk A J
References (47)
47 references, click to expand
  1. Quantitative film detection of 3H and 14C in polyacrylamide gels by fluorography.
    Eur J Biochem. 1975 Aug 15;56(2):335-41 PMID: 1175627
  2. Mapping of a gene coding for a major late structural polypeptide on the vaccinia virus genome.
    J Virol. 1984 Feb;49(2):371-8 PMID: 6319738
  3. Transformation of mammalian cells with genes from procaryotes and eucaryotes.
    Cell. 1979 Apr;16(4):777-85 PMID: 222468
  4. Isolation of adenovirus type 5 host range deletion mutants defective for transformation of rat embryo cells.
    Cell. 1979 Jul;17(3):683-9 PMID: 476833
  5. Pre-early adenovirus 5 gene product regulates synthesis of early viral messenger RNAs.
    Cell. 1979 Aug;17(4):935-44 PMID: 487437
  6. Plasmid cloning vehicles derived from plasmids ColE1, F, R6K, and RK2.
    Methods Enzymol. 1979;68:268-80 PMID: 232215
  7. SV40-transformed simian cells support the replication of early SV40 mutants.
    Cell. 1981 Jan;23(1):175-82 PMID: 6260373
  8. Mapping a eukaryotic promoter: a DNA sequence required for in vivo expression of adenovirus pre-early functions.
    Proc Natl Acad Sci U S A. 1981 Mar;78(3):1381-5 PMID: 6262792
  9. Adenovirus type 5 early region 1b gene product is required for efficient shutoff of host protein synthesis.
    J Virol. 1984 Apr;50(1):202-12 PMID: 6142122
  10. Complete transformation by adenovirus 2 requires both E1A proteins.
    Cell. 1984 Apr;36(4):951-61 PMID: 6705049
  11. Individual products of the adenovirus 12S and 13S EIa mRNAs stimulate viral EIIa and EIII expression at the transcriptional level.
    Proc Natl Acad Sci U S A. 1984 Jul;81(14):4381-5 PMID: 6336330
  12. Dissection of overlapping functions within the adenovirus type 5 E1A gene.
    EMBO J. 1984 Aug;3(8):1907-12 PMID: 6479152
  13. Transcription control region within the protein-coding portion of adenovirus E1A genes.
    Mol Cell Biol. 1984 Jul;4(7):1293-305 PMID: 6334230
  14. Introduction, stable integration, and controlled expression of a chimeric adenovirus gene whose product is toxic to the recipient human cell.
    Mol Cell Biol. 1984 Jul;4(7):1354-62 PMID: 6542172
  15. Transcription control by oncogenes.
    Cell. 1985 May;41(1):3-5 PMID: 2986847
  16. Enhancement of RNA polymerase III transcription by the E1A gene product of adenovirus.
    Cell. 1985 Jul;41(3):955-63 PMID: 4005953
  17. Two distinct transcription factors bind to the HSV thymidine kinase promoter in vitro.
    Cell. 1985 Sep;42(2):559-72 PMID: 2992804
  18. Identification of a cellular transcription factor involved in E1A trans-activation.
    Cell. 1986 Apr 25;45(2):219-28 PMID: 2938741
  19. Adenovirus stimulation of transcription by RNA polymerase III: evidence for an E1A-dependent increase in transcription factor IIIC concentration.
    EMBO J. 1986 Feb;5(2):343-54 PMID: 2940084
  20. E1A 13S and 12S mRNA products made in Escherichia coli both function as nucleus-localized transcription activators but do not directly bind DNA.
    Mol Cell Biol. 1985 Oct;5(10):2653-61 PMID: 2942760
  21. Activation of the human beta-interferon gene requires an interferon-inducible factor.
    Mol Cell Biol. 1986 Mar;6(3):801-10 PMID: 3773893
  22. Progressive reorganization of the host cell cytoskeleton during adenovirus infection.
    J Virol. 1986 Dec;60(3):1186-91 PMID: 3023671
  23. The adenovirus E1B-55K transforming polypeptide modulates transport or cytoplasmic stabilization of viral and host cell mRNAs.
    Mol Cell Biol. 1986 Feb;6(2):470-6 PMID: 2946932
  24. Stimulation of the adenovirus E2 promoter by simian virus 40 T antigen or E1A occurs by different mechanisms.
    Mol Cell Biol. 1986 Jun;6(6):2020-6 PMID: 3023915
  25. Adenovirus promoters and E1A transactivation.
    Annu Rev Genet. 1986;20:45-79 PMID: 3028247
  26. Alterations in nuclear matrix structure after adenovirus infection.
    J Virol. 1987 Apr;61(4):1007-18 PMID: 3820360
  27. Glucocorticoids enhance stability of human growth hormone mRNA.
    Mol Cell Biol. 1987 Apr;7(4):1496-507 PMID: 3037323
  28. Selective induction of human heat shock gene transcription by the adenovirus E1A gene products, including the 12S E1A product.
    Mol Cell Biol. 1987 Aug;7(8):2884-90 PMID: 2959854
  29. Oestrogen and glucocorticoid responsive elements are closely related but distinct.
    Nature. 1987 Oct 22-28;329(6141):734-6 PMID: 3670376
  30. Upstream regulatory regions required to stabilize binding to the TATA sequence in an adenovirus early promoter.
    Nucleic Acids Res. 1987 Oct 26;15(20):8367-85 PMID: 2959908
  31. Activation of adenovirus 5 E1A transcription by region E1B in transformed primary rat cells.
    EMBO J. 1987 Nov;6(11):3399-405 PMID: 2962857
  32. Adenovirus transforming 19-kD T antigen has an enhancer-dependent trans-activation function and relieves enhancer repression mediated by viral and cellular genes.
    Genes Dev. 1987 Sep;1(7):645-58 PMID: 2962899
  33. Expression of transfected vimentin genes in differentiating murine erythroleukemia cells reveals divergent cis-acting regulation of avian and mammalian vimentin sequences.
    Mol Cell Biol. 1987 Nov;7(11):3955-70 PMID: 3481037
  34. Identification of an E1A-inducible cellular factor that interacts with regulatory sequences within the adenovirus E4 promoter.
    EMBO J. 1987 Dec 20;6(13):4073-81 PMID: 2965007
  35. Factors responsible for the higher transcriptional activity of extracts of adenovirus-infected cells fractionate with the TATA box transcription factor.
    Mol Cell Biol. 1988 Apr;8(4):1765-74 PMID: 2967913
  36. A small-scale procedure for preparation of nuclear extracts that support efficient transcription and pre-mRNA splicing.
    Gene Anal Tech. 1988 Mar-Apr;5(2):22-31 PMID: 3192155
  37. Glucocorticoids regulate expression of dihydrofolate reductase cDNA in mouse mammary tumour virus chimaeric plasmids.
    Nature. 1981 Nov 19;294(5838):228-32 PMID: 6272123
  38. Resolving the functions of overlapping viral genes by site-specific mutagenesis at a mRNA splice site.
    Nature. 1982 Feb 4;295(5848):380-4 PMID: 7057903
  39. Mechanism of activation of early viral transcription by the adenovirus E1A gene product.
    Cell. 1981 Oct;26(2 Pt 2):213-20 PMID: 7332929
  40. Transformation of mammalian cells to antibiotic resistance with a bacterial gene under control of the SV40 early region promoter.
    J Mol Appl Genet. 1982;1(4):327-41 PMID: 6286831
  41. Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei.
    Nucleic Acids Res. 1983 Mar 11;11(5):1475-89 PMID: 6828386
  42. Expression of adenovirus type 12 early region 1 in KB cells transformed by recombinants containing the gene.
    J Virol. 1983 Mar;45(3):1074-82 PMID: 6834475
  43. Expression of adenovirus E1a and E1b gene products and the Escherichia coli XGPRT gene in KB cells.
    J Virol. 1983 May;46(2):454-65 PMID: 6341621
  44. Cis-acting induction of adenovirus transcription.
    Cell. 1983 Jul;33(3):683-93 PMID: 6871990
  45. A cell line that supports the growth of a defective early region 4 deletion mutant of human adenovirus type 2.
    Proc Natl Acad Sci U S A. 1983 Sep;80(17):5383-6 PMID: 6310575
  46. Analysis of adenovirus transforming proteins from early regions 1A and 1B with antisera to inducible fusion antigens produced in Escherichia coli.
    J Virol. 1984 Jan;49(1):132-41 PMID: 6361277
  47. Characteristics of a human cell line transformed by DNA from human adenovirus type 5.
    J Gen Virol. 1977 Jul;36(1):59-74 PMID: 886304
Article Info
Journal
Molecular and cellular biology
Abbr.
Mol Cell Biol
ISSN
0270-7306
Published
1988-11-00
Pages
4799-807
Language
English
Region
United States
NLM ID
8109087
PMCID
PMC365573
Subset
IM
Grants
NCI NIH HHS · CA41062 · United States
NIGMS NIH HHS · GM10699 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]