Literature DB >> 2833024

The enhancer elements and GGGCGG boxes of SV40 provide similar functions in bidirectionally promoting transcription.

G Z Hertz1, J E Mertz.   

Abstract

The early and the late genes of simian virus 40 (SV40) are transcribed in opposite directions from a shared promoter region. The 72- and the 21-bp repeat regions of the SV40 genome contain the transcriptional enhancer and six copies of the Sp 1-binding GGGCGG box, respectively. SV40 mutants lacking various parts of these regions were examined in COS cells to determine the importance of these sequences for transcription in each direction. We made the following observations. (i) The 72-bp repeat region was required for efficient transcription of both the early and the late genes. (ii) The 21-bp repeat region was required for efficient early-gene transcription, but not for efficient late-gene transcription; however, it was able to supply some late-promoter activity when the 72-bp repeat region was missing. (iii) The ability of either of these regions to promote transcription was gradually reduced as the number of promoter elements within each was decreased. (iv) Mutations in these regions always decreased early-gene transcription more than late-gene transcription. These results indicate that both regions are made up of multiple bidirectional promoter elements, but that the 72-bp repeat region is more effective at inducing transcription than the 21-bp repeat region. Since each region can also (i) satisfy a need for promoter elements in the replication of viral DNA and (ii) induce a region of open chromatin, we conclude that the promoter elements within the enhancer and the GGGCGG boxes probably provide similar functions.

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Year:  1988        PMID: 2833024     DOI: 10.1016/0042-6822(88)90299-1

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  9 in total

1.  Simian virus 40 late transcripts lacking excisable intervening sequences are defective in both stability in the nucleus and transport to the cytoplasm.

Authors:  W S Ryu; J E Mertz
Journal:  J Virol       Date:  1989-10       Impact factor: 5.103

2.  Stable growth of simian virus 40 recombinants containing multimerized enhancers.

Authors:  B Ondek; W Herr
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

3.  Programmed factor binding to simian virus 40 GC-box replication and transcription control sequences.

Authors:  R L Buchanan; J D Gralla
Journal:  J Virol       Date:  1990-01       Impact factor: 5.103

4.  Characterization of a minimal simian virus 40 late promoter: enhancer elements in the 72-base-pair repeat not required.

Authors:  W S Dynan; S A Chervitz
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

5.  Direct modulation of simian virus 40 late gene expression by thyroid hormone and its receptor.

Authors:  F Zuo; R J Kraus; T Gulick; D D Moore; J E Mertz
Journal:  J Virol       Date:  1997-01       Impact factor: 5.103

6.  In situ nucleoprotein structure involving origin-proximal SV40 DNA control elements.

Authors:  L Zhang; J D Gralla
Journal:  Nucleic Acids Res       Date:  1990-04-11       Impact factor: 16.971

7.  Two synthetic Sp1-binding sites functionally substitute for the 21-base-pair repeat region to activate simian virus 40 growth in CV-1 cells.

Authors:  J Lednicky; W R Folk
Journal:  J Virol       Date:  1992-11       Impact factor: 5.103

8.  Simian virus 40 late gene expression is regulated by members of the steroid/thyroid hormone receptor superfamily.

Authors:  F Zuo; J E Mertz
Journal:  Proc Natl Acad Sci U S A       Date:  1995-09-12       Impact factor: 11.205

9.  CGGBP1-dependent CTCF-binding sites restrict ectopic transcription.

Authors:  Divyesh Patel; Manthan Patel; Subhamoy Datta; Umashankar Singh
Journal:  Cell Cycle       Date:  2021-09-29       Impact factor: 5.173

  9 in total

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