Literature DB >> 6090561

Multiple control elements involved in the initiation of SV40 late transcription.

D C Rio, R Tjian.   

Abstract

Mutants with deletions in the control region of simian virus 40 (SV40) were tested for their ability to direct late transcription in a nuclear extract derived from HeLa cells. Primer extension analysis revealed that late SV40 transcription initiates predominantly at two sites in vitro, one of which corresponds to the major in vivo start site at nucleotide 325, while the other site is located at nucleotide 170. A series of 5',3', and internal deletions of the putative promoter region were used to define two distinct control elements that appear to function independently of each other and that are located upstream from each of the in vitro initiation sites. In addition, transcription from the initiation site at 325 is also influenced by GC-rich sequences (CCGCCC) found within a regulatory region that consists of two 21 bp perfect repeats and a third degenerate repeat located 250 bp upstream from the major late initiation site. These six upstream GC blocks, which lie directly upstream from the initiation site at 170, also affect transcription from this start site. Although these 21 bp repeats are known to be an important part of the SV40 early promoter, our findings suggest that they are also involved in modulating the levels of late transcription in vitro.

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Year:  1984        PMID: 6090561

Source DB:  PubMed          Journal:  J Mol Appl Genet        ISSN: 0271-6801


  16 in total

1.  Specific stimulation of simian virus 40 late transcription in vitro by a cellular factor binding the simian virus 40 21-base-pair repeat promoter element.

Authors:  C H Kim; C Heath; A Bertuch; U Hansen
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

2.  Inhibition of rRNA synthesis by poliovirus: specific inactivation of transcription factors.

Authors:  S J Rubinstein; A Dasgupta
Journal:  J Virol       Date:  1989-11       Impact factor: 5.103

3.  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

4.  Contribution of different GC-motifs to the control of simian virus 40 late promoter activity.

Authors:  M Ernoult-Lange; F Omilli; E May
Journal:  Nucleic Acids Res       Date:  1987-10-26       Impact factor: 16.971

5.  Activity of simian virus 40 late promoter elements in the absence of large T antigen: evidence for repression of late gene expression.

Authors:  J C Alwine; J Picardi
Journal:  J Virol       Date:  1986-11       Impact factor: 5.103

6.  Sequences involved in initiation of simian virus 40 late transcription in the absence of T antigen.

Authors:  F Omilli; M Ernoult-Lange; J Borde; E May
Journal:  Mol Cell Biol       Date:  1986-06       Impact factor: 4.272

7.  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.

Authors:  M Ernoult-Lange; F Omilli; D R O'Reilly; E May
Journal:  J Virol       Date:  1987-01       Impact factor: 5.103

8.  Analysis of an activatable promoter: sequences in the simian virus 40 late promoter required for T-antigen-mediated trans activation.

Authors:  J M Keller; J C Alwine
Journal:  Mol Cell Biol       Date:  1985-08       Impact factor: 4.272

9.  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

10.  A primer vector system that allows temperature dependent gene amplification and expression in mammalian cells: regulation of the influenza virus NS1 gene expression.

Authors:  A Portela; J A Melero; C Martínez; E Domingo; J Ortín
Journal:  Nucleic Acids Res       Date:  1985-11-25       Impact factor: 16.971

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