Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1996 Oct 15;24(20):3887–3895. doi: 10.1093/nar/24.20.3887

Chromatin structure and factor site occupancies in an in vivo-assembled transcription elongation complex.

J K Eadara 1, K G Hadlock 1, L C Lutter 1
PMCID: PMC146202  PMID: 8918788

Abstract

The chromatin structure specific to the SV40 late transcription elongation complex as well as the occupancy of several sites that bind transcription factors have been examined. These features have been determined by assessing blockage to restriction enzyme digestion. Cleavage specific to the elongation complex has been quantified using ternary complex analysis. This method involves radioactively labeling the complex by in vitro transcription followed by determining the extent of linearization by electrophoresis in an agarose gel. It was found that not only is the origin region devoid of nucleosomes, but there is also no stable factor occupancy at the BglI, SphI, KpnI and MspI restriction enzyme sites within this region. Thus these sites were cleaved to a high degree, meaning that the binding sites for a number of transcription factors, including OBP/TEF-1, TBP, DAP, as well as a proposed positioned nucleosome, are unoccupied in the native viral transcription elongation complex. The absence of these trans-acting factors from their respective binding sites in the elongation complex indicates that they bind only transiently, possibly cycling on and off during the transcription cycle. This finding implies that various forms of transcription complex are assembled and disassembled during transcription and thus supports a 'hit-and-run' model of factor function.

Full Text

The Full Text of this article is available as a PDF (191.6 KB).

Selected References

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

  1. Ambrose C., Blasquez V., Bina M. A block in initiation of simian virus 40 assembly results in the accumulation of minichromosomes containing an exposed regulatory region. Proc Natl Acad Sci U S A. 1986 May;83(10):3287–3291. doi: 10.1073/pnas.83.10.3287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Ayer D. E., Dynan W. S. A downstream-element-binding factor facilitates assembly of a functional preinitiation complex at the simian virus 40 major late promoter. Mol Cell Biol. 1990 Jul;10(7):3635–3645. doi: 10.1128/mcb.10.7.3635. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Ayer D. E., Dynan W. S. Simian virus 40 major late promoter: a novel tripartite structure that includes intragenic sequences. Mol Cell Biol. 1988 May;8(5):2021–2033. doi: 10.1128/mcb.8.5.2021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Batson S. C., Rimsky S., Sundseth R., Hansen U. Association of nucleosome-free regions and basal transcription factors with in vivo-assembled chromatin templates active in vitro. Nucleic Acids Res. 1993 Jul 25;21(15):3459–3468. doi: 10.1093/nar/21.15.3459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Beard P., Bruggmann H. A transcription factor from simian virus 40 chromosomes which activates the viral late promoter in vitro. J Virol. 1988 Nov;62(11):4296–4302. doi: 10.1128/jvi.62.11.4296-4302.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Beard P. Mobility of histones on the chromosome of simian virus 40. Cell. 1978 Nov;15(3):955–967. doi: 10.1016/0092-8674(78)90279-9. [DOI] [PubMed] [Google Scholar]
  7. Buchanan R. L., Gralla J. D. Programmed factor binding to simian virus 40 GC-box replication and transcription control sequences. J Virol. 1990 Jan;64(1):347–353. doi: 10.1128/jvi.64.1.347-353.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Casaz P., Sundseth R., Hansen U. trans activation of the simian virus 40 late promoter by large T antigen requires binding sites for the cellular transcription factor TEF-1. J Virol. 1991 Dec;65(12):6535–6543. doi: 10.1128/jvi.65.12.6535-6543.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cereghini S., Yaniv M. Assembly of transfected DNA into chromatin: structural changes in the origin-promoter-enhancer region upon replication. EMBO J. 1984 Jun;3(6):1243–1253. doi: 10.1002/j.1460-2075.1984.tb01959.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Choder M., Bratosin S., Aloni Y. A direct analysis of transcribed minichromosomes: all transcribed SV40 minichromosomes have a nuclease-hypersensitive region within a nucleosome-free domain. EMBO J. 1984 Dec 1;3(12):2929–2936. doi: 10.1002/j.1460-2075.1984.tb02234.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Davidson I., Xiao J. H., Rosales R., Staub A., Chambon P. The HeLa cell protein TEF-1 binds specifically and cooperatively to two SV40 enhancer motifs of unrelated sequence. Cell. 1988 Sep 23;54(7):931–942. doi: 10.1016/0092-8674(88)90108-0. [DOI] [PubMed] [Google Scholar]
  12. Eadara J. K., Lutter L. C. Determination of occupancies of the SPH and GT-IIC transcription factor binding motifs in SV40: evidence for two forms of transcription elongation complex. Virology. 1996 Sep 1;223(1):120–131. doi: 10.1006/viro.1996.0461. [DOI] [PubMed] [Google Scholar]
  13. Eadara J. K., Lutter L. C. RNA polymerase locations in the simian virus 40 transcription complex. J Biol Chem. 1993 Oct 15;268(29):22020–22027. [PubMed] [Google Scholar]
  14. Ernoult-Lange M., Omilli F., O'Reilly D. R., May E. Characterization of the simian virus 40 late promoter: relative importance of sequences within the 72-base-pair repeats differs before and after viral DNA replication. J Virol. 1987 Jan;61(1):167–176. doi: 10.1128/jvi.61.1.167-176.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Felsenfeld G. Chromatin as an essential part of the transcriptional mechanism. Nature. 1992 Jan 16;355(6357):219–224. doi: 10.1038/355219a0. [DOI] [PubMed] [Google Scholar]
  16. Gallo G. J., Gilinger G., Alwine J. C. Simian virus 40 T antigen alters the binding characteristics of specific simian DNA-binding factors. Mol Cell Biol. 1988 Apr;8(4):1648–1656. doi: 10.1128/mcb.8.4.1648. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Gallo G. J., Gruda M. C., Manuppello J. R., Alwine J. C. Activity of simian DNA-binding factors is altered in the presence of simian virus 40 (SV40) early proteins: characterization of factors binding to elements involved in activation of the SV40 late promoter. J Virol. 1990 Jan;64(1):173–184. doi: 10.1128/jvi.64.1.173-184.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Gruda M. C., Zabolotny J. M., Xiao J. H., Davidson I., Alwine J. C. Transcriptional activation by simian virus 40 large T antigen: interactions with multiple components of the transcription complex. Mol Cell Biol. 1993 Feb;13(2):961–969. doi: 10.1128/mcb.13.2.961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Hadlock K. G., Lutter L. C. T-antigen is not bound to the replication origin of the simian virus 40 late transcription complex. J Mol Biol. 1990 Sep 5;215(1):53–65. doi: 10.1016/S0022-2836(05)80094-4. [DOI] [PubMed] [Google Scholar]
  20. Hadlock K. G., Quasney M. W., Lutter L. C. Immunoprecipitation of the simian virus 40 late transcription complex with antibody against T-antigen. J Biol Chem. 1987 Nov 15;262(32):15527–15537. [PubMed] [Google Scholar]
  21. Hartzell S. W., Byrne B. J., Subramanian K. N. Mapping of the late promoter of simian virus 40. Proc Natl Acad Sci U S A. 1984 Jan;81(1):23–27. doi: 10.1073/pnas.81.1.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Hay N., Aloni Y. Attenuation in SV40 as a mechanism of transcription-termination by RNA polymerase B. Nucleic Acids Res. 1984 Feb 10;12(3):1401–1414. doi: 10.1093/nar/12.3.1401. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Herr W., Gluzman Y. Duplications of a mutated simian virus 40 enhancer restore its activity. Nature. 1985 Feb 21;313(6004):711–714. doi: 10.1038/313711a0. [DOI] [PubMed] [Google Scholar]
  24. Hsieh C. H., Griffith J. D. The terminus of SV40 DNA replication and transcription contains a sharp sequence-directed curve. Cell. 1988 Feb 26;52(4):535–544. doi: 10.1016/0092-8674(88)90466-7. [DOI] [PubMed] [Google Scholar]
  25. Huang H. C., Sundseth R., Hansen U. Transcription factor LSF binds two variant bipartite sites within the SV40 late promoter. Genes Dev. 1990 Feb;4(2):287–298. doi: 10.1101/gad.4.2.287. [DOI] [PubMed] [Google Scholar]
  26. Jakobovits E. B., Bratosin S., Aloni Y. A nucleosome-free region in SV40 minichromosomes. Nature. 1980 May 22;285(5762):263–265. doi: 10.1038/285263a0. [DOI] [PubMed] [Google Scholar]
  27. Jones N. C., Rigby P. W., Ziff E. B. Trans-acting protein factors and the regulation of eukaryotic transcription: lessons from studies on DNA tumor viruses. Genes Dev. 1988 Mar;2(3):267–281. doi: 10.1101/gad.2.3.267. [DOI] [PubMed] [Google Scholar]
  28. Keller J. M., Alwine J. C. Analysis of an activatable promoter: sequences in the simian virus 40 late promoter required for T-antigen-mediated trans activation. Mol Cell Biol. 1985 Aug;5(8):1859–1869. doi: 10.1128/mcb.5.8.1859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Llopis R., Perrin F., Bellard F., Gariglio P. Quantitation of transcribing native simian virus 40 minichromosomes extracted from CV1 cells late in infection. J Virol. 1981 Apr;38(1):82–90. doi: 10.1128/jvi.38.1.82-90.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Lutter L. C. DNase II digestion of the nucleosome core: precise locations and relative exposures of sites. Nucleic Acids Res. 1981 Sep 11;9(17):4251–4265. doi: 10.1093/nar/9.17.4251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Lutter L. C., Halvorson H. R., Calladine C. R. Topological measurement of protein-induced DNA bend angles. J Mol Biol. 1996 Sep 6;261(5):620–633. doi: 10.1006/jmbi.1996.0488. [DOI] [PubMed] [Google Scholar]
  32. Lutter L. C. Thermal unwinding of simian virus 40 transcription complex DNA. Proc Natl Acad Sci U S A. 1989 Nov;86(22):8712–8716. doi: 10.1073/pnas.86.22.8712. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. May E., Omilli F., Ernoult-Lange M., Zenke M., Chambon P. The sequence motifs that are involved in SV40 enhancer function also control SV40 late promoter activity. Nucleic Acids Res. 1987 Mar 25;15(6):2445–2461. doi: 10.1093/nar/15.6.2445. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. McKnight S., Tjian R. Transcriptional selectivity of viral genes in mammalian cells. Cell. 1986 Sep 12;46(6):795–805. doi: 10.1016/0092-8674(86)90061-9. [DOI] [PubMed] [Google Scholar]
  35. Mitchell P. J., Tjian R. Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins. Science. 1989 Jul 28;245(4916):371–378. doi: 10.1126/science.2667136. [DOI] [PubMed] [Google Scholar]
  36. Petryniak B., Lutter L. C. Topological characterization of the simian virus 40 transcription complex. Cell. 1987 Jan 30;48(2):289–295. doi: 10.1016/0092-8674(87)90432-6. [DOI] [PubMed] [Google Scholar]
  37. Poljak L. G., Gralla J. D. Competition for formation of nucleosomes on fragmented SV40 DNA: a hyperstable nucleosome forms on the termination region. Biochemistry. 1987 Jan 13;26(1):295–303. doi: 10.1021/bi00375a041. [DOI] [PubMed] [Google Scholar]
  38. Powers J. H., Bina M. In vitro assembly of a positioned nucleosome near the hypersensitive region in simian virus 40 chromatin. J Mol Biol. 1991 Oct 5;221(3):795–803. doi: 10.1016/0022-2836(91)80176-u. [DOI] [PubMed] [Google Scholar]
  39. Rigaud G., Roux J., Pictet R., Grange T. In vivo footprinting of rat TAT gene: dynamic interplay between the glucocorticoid receptor and a liver-specific factor. Cell. 1991 Nov 29;67(5):977–986. doi: 10.1016/0092-8674(91)90370-e. [DOI] [PubMed] [Google Scholar]
  40. Ryder K., Silver S., DeLucia A. L., Fanning E., Tegtmeyer P. An altered DNA conformation in origin region I is a determinant for the binding of SV40 large T antigen. Cell. 1986 Mar 14;44(5):719–725. doi: 10.1016/0092-8674(86)90838-x. [DOI] [PubMed] [Google Scholar]
  41. Saragosti S., Cereghini S., Yaniv M. Fine structure of the regulatory region of simian virus 40 minichromosomes revealed by DNAase I digestion. J Mol Biol. 1982 Sep 15;160(2):133–146. doi: 10.1016/0022-2836(82)90171-1. [DOI] [PubMed] [Google Scholar]
  42. Saragosti S., Moyne G., Yaniv M. Absence of nucleosomes in a fraction of SV40 chromatin between the origin of replication and the region coding for the late leader RNA. Cell. 1980 May;20(1):65–73. doi: 10.1016/0092-8674(80)90235-4. [DOI] [PubMed] [Google Scholar]
  43. Scott W. A., Walter C. F., Cryer B. L. Barriers to nuclease Bal31 digestion across specific sites in simian virus 40 chromatin. Mol Cell Biol. 1984 Apr;4(4):604–610. doi: 10.1128/mcb.4.4.604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Scott W. A., Wigmore D. J. Sites in simian virus 40 chromatin which are preferentially cleaved by endonucleases. Cell. 1978 Dec;15(4):1511–1518. doi: 10.1016/0092-8674(78)90073-9. [DOI] [PubMed] [Google Scholar]
  45. Spadafora C., Oudet P., Chambon P. Rearrangement of chromatin structure induced by increasing ionic strength and temperature. Eur J Biochem. 1979 Oct;100(1):225–235. doi: 10.1111/j.1432-1033.1979.tb02053.x. [DOI] [PubMed] [Google Scholar]
  46. Sturm R., Baumruker T., Franza B. R., Jr, Herr W. A 100-kD HeLa cell octamer binding protein (OBP100) interacts differently with two separate octamer-related sequences within the SV40 enhancer. Genes Dev. 1987 Dec;1(10):1147–1160. doi: 10.1101/gad.1.10.1147. [DOI] [PubMed] [Google Scholar]
  47. Tack L. C., Wassarman P. M., DePamphilis M. L. Chromatin assembly. Relationship of chromatin structure to DNA sequence during simian virus 40 replication. J Biol Chem. 1981 Aug 25;256(16):8821–8828. [PubMed] [Google Scholar]
  48. Tjian R., Maniatis T. Transcriptional activation: a complex puzzle with few easy pieces. Cell. 1994 Apr 8;77(1):5–8. doi: 10.1016/0092-8674(94)90227-5. [DOI] [PubMed] [Google Scholar]
  49. Varshavsky A. J., Sundin O., Bohn M. A stretch of "late" SV40 viral DNA about 400 bp long which includes the origin of replication is specifically exposed in SV40 minichromosomes. Cell. 1979 Feb;16(2):453–466. doi: 10.1016/0092-8674(79)90021-7. [DOI] [PubMed] [Google Scholar]
  50. Wiley S. R., Kraus R. J., Mertz J. E. Functional binding of the "TATA" box binding component of transcription factor TFIID to the -30 region of TATA-less promoters. Proc Natl Acad Sci U S A. 1992 Jul 1;89(13):5814–5818. doi: 10.1073/pnas.89.13.5814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Wiley S. R., Kraus R. J., Zuo F., Murray E. E., Loritz K., Mertz J. E. SV40 early-to-late switch involves titration of cellular transcriptional repressors. Genes Dev. 1993 Nov;7(11):2206–2219. doi: 10.1101/gad.7.11.2206. [DOI] [PubMed] [Google Scholar]
  52. Wolffe A. P., Brown D. D. Developmental regulation of two 5S ribosomal RNA genes. Science. 1988 Sep 23;241(4873):1626–1632. doi: 10.1126/science.241.4873.1626. [DOI] [PubMed] [Google Scholar]
  53. Xiao J. H., Davidson I., Matthes H., Garnier J. M., Chambon P. Cloning, expression, and transcriptional properties of the human enhancer factor TEF-1. Cell. 1991 May 17;65(4):551–568. doi: 10.1016/0092-8674(91)90088-g. [DOI] [PubMed] [Google Scholar]
  54. Zawel L., Reinberg D. Common themes in assembly and function of eukaryotic transcription complexes. Annu Rev Biochem. 1995;64:533–561. doi: 10.1146/annurev.bi.64.070195.002533. [DOI] [PubMed] [Google Scholar]
  55. Zhang L., Gralla J. D. In situ nucleoprotein structure at the SV40 major late promoter: melted and wrapped DNA flank the start site. Genes Dev. 1989 Nov;3(11):1814–1822. doi: 10.1101/gad.3.11.1814. [DOI] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES