Literature DB >> 3037380

A factor discriminating between the wild-type and a mutant polyomavirus enhancer.

I Kovesdi, M Satake, K Furukawa, R Reichel, Y Ito, J R Nevins.   

Abstract

Enhancers increase the frequency of transcription initiation from linked promoter elements, most probably as a result of the binding of specific proteins to the enhancer. The polyomavirus early region is expressed in differentiated mouse cells but not in undifferentiated embryonal carcinoma (EC) cells. This host range is a function of the enhancer because polyomavirus mutants selected for growth in EC cells have mutations in the enhancer and the host range is reproduced in transfection assays using the mutant enhancers. To understand the basis for this alteration in enhancer function, we have assayed extracts of EC cells for proteins that can interact with this sequence. We have detected a protein, present in a variety of cells, that can bind to the F441 mutant sequence, but binds only very poorly to the wild-type sequence. We conclude that this sequence alteration has probably generated a binding site for a positive-acting factor that allows the enhancer to function.

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Year:  1987        PMID: 3037380     DOI: 10.1038/328087a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  23 in total

1.  Biological activities of oligonucleotides spanning the F9 point mutation within the enhancer region of polyomavirus DNA.

Authors:  M Satake; K Furukawa; Y Ito
Journal:  J Virol       Date:  1988-03       Impact factor: 5.103

2.  Host range specificity of polyomavirus EC mutants in mouse embryonal carcinoma and embryonal stem cells and preimplantation embryos.

Authors:  F Mélin; R Kemler; C Kress; H Pinon; D Blangy
Journal:  J Virol       Date:  1991-06       Impact factor: 5.103

3.  Deletion analysis of the polyomavirus late promoter: evidence for both positive and negative elements in the absence of early proteins.

Authors:  K B Cahill; G G Carmichael
Journal:  J Virol       Date:  1989-09       Impact factor: 5.103

4.  Two overlapping sequence motifs within the polyomavirus enhancer are independently the targets of stimulation by both the tumor promoter 12-O-tetradecanoylphorbol-13-acetate and the Ha-ras oncogene.

Authors:  Y Yamaguchi; M Satake; Y Ito
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

5.  Numerous nuclear proteins bind the long control region of human papillomavirus type 16: a subset of 6 of 23 DNase I-protected segments coincides with the location of the cell-type-specific enhancer.

Authors:  B Gloss; T Chong; H U Bernard
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

6.  Asp-286----Asn-286 in polyomavirus large T antigen relaxes the specificity of binding to the polyomavirus origin.

Authors:  W J Tang; W R Folk
Journal:  J Virol       Date:  1989-01       Impact factor: 5.103

7.  Stimulation of transcription in vitro by binding sites for nuclear factor I.

Authors:  R M Gronostajski; J Knox; D Berry; N G Miyamoto
Journal:  Nucleic Acids Res       Date:  1988-03-25       Impact factor: 16.971

8.  Promoter upstream elements of the chicken cardiac myosin light-chain 2-A gene interact with trans-acting regulatory factors for muscle-specific transcription.

Authors:  T Braun; E Tannich; G Buschhausen-Denker; H H Arnold
Journal:  Mol Cell Biol       Date:  1989-06       Impact factor: 4.272

9.  Point mutation in the polyomavirus enhancer alters local DNA conformation.

Authors:  F K Fujimura
Journal:  Nucleic Acids Res       Date:  1988-03-25       Impact factor: 16.971

10.  Multiple domains in the polyomavirus B enhancer are required for productive infection of F9 embryonal carcinoma cells.

Authors:  R W Tseng; F K Fujimura
Journal:  J Virol       Date:  1988-08       Impact factor: 5.103

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