Literature DB >> 2828692

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

M Satake1, K Furukawa, Y Ito.   

Abstract

A mutant of polyomavirus, F441, selected to grow in undifferentiated mouse F9 embryonal carcinoma cells, carries a single-base change in the enhancer region at nucleotide (nt) 5233 of the viral genome. Enhancers of most of the F9 mutants have a duplicated segment of viral DNA encompassing nt 5233. The minimum duplicated segment of all the known F9 mutants is from nt 5218 to nt 5239. We prepared oligonucleotides spanning the sequence from nt 5218 through nt 5239 of the genome of the wild type and F441 and examined the biological activities of the oligonucleotides by a transient assay of chloramphenicol acetyltransferase (CAT) gene expression in F9 cells. The oligonucleotide harboring the F441 mutation was shown to increase cat gene expression in F9 cells when linked at an upstream position in both orientations. When dimerized at an upstream position, the F441 oligonucleotide showed even higher cat gene expression enhancing activity. In contrast, no such effects were observed with the oligonucleotide of the wild-type sequence. In addition, the F441 oligonucleotide, but not the wild-type sequence, could inhibit the activity of whole enhancer fragment of F441 when cotransfected into F9 cells in excess amounts. On the basis of the results obtained, we suggest that the segment of F441 enhancer encompassing the point mutation contains a target for a cellular factor(s) which acts in a positive manner to increase the transcription of a gene in undifferentiated mouse F9 cells.

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Year:  1988        PMID: 2828692      PMCID: PMC253656          DOI: 10.1128/JVI.62.3.970-977.1988

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  46 in total

1.  Expression of polyoma virus in heterokaryons between embryonal carcinoma cells and differentiated cells.

Authors:  M Boccara; F Kelly
Journal:  Virology       Date:  1978-10-01       Impact factor: 3.616

2.  Neoplastic differentiation: interaction of simian virus 40 and polyoma virus with murine teratocarcinoma cells in vitro.

Authors:  D E Swartzendruber; J M Lehman
Journal:  J Cell Physiol       Date:  1975-04       Impact factor: 6.384

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

Authors:  I Kovesdi; M Satake; K Furukawa; R Reichel; Y Ito; J R Nevins
Journal:  Nature       Date:  1987 Jul 2-8       Impact factor: 49.962

4.  Biochemical transfer of single-copy eucaryotic genes using total cellular DNA as donor.

Authors:  M Wigler; A Pellicer; S Silverstein; R Axel
Journal:  Cell       Date:  1978-07       Impact factor: 41.582

5.  The induction of differentiation in teratocarcinoma stem cells by retinoic acid.

Authors:  S Strickland; V Mahdavi
Journal:  Cell       Date:  1978-10       Impact factor: 41.582

Review 6.  Mouse teratocarcinoma and embryonic antigens.

Authors:  F Jacob
Journal:  Immunol Rev       Date:  1977-01       Impact factor: 12.988

7.  Coding potential and regulatory signals of the polyoma virus genome.

Authors:  E Soeda; J R Arrand; N Smolar; J E Walsh; B E Griffin
Journal:  Nature       Date:  1980-01-31       Impact factor: 49.962

8.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

9.  Selection of mouse neuroblastoma cell-specific polyoma virus mutants with stage differentiative advantages of replication.

Authors:  R Maione; C Passananti; V De Simone; P Delli-Bovi; G Augusti-Tocco; P Amati
Journal:  EMBO J       Date:  1985-12-01       Impact factor: 11.598

10.  Multiple sequence motifs are involved in SV40 enhancer function.

Authors:  M Zenke; T Grundström; H Matthes; M Wintzerith; C Schatz; A Wildeman; P Chambon
Journal:  EMBO J       Date:  1986-02       Impact factor: 11.598

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  6 in total

1.  Loss of responsiveness of an AP1-related factor, PEBP1, to 12-O-tetradecanoylphorbol-13-acetate after transformation of NIH 3T3 cells by the Ha-ras oncogene.

Authors:  M Satake; T Ibaraki; Y Yamaguchi; Y Ito
Journal:  J Virol       Date:  1989-09       Impact factor: 5.103

2.  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

3.  Transacting activities of the E7 genes of several types of human papillomavirus.

Authors:  T Ibaraki; M Satake; N Kurai; M Ichijo; Y Ito
Journal:  Virus Genes       Date:  1993-06       Impact factor: 2.332

4.  The nuclear protooncogenes c-jun and c-fos as regulators of DNA replication.

Authors:  Y Murakami; M Satake; Y Yamaguchi-Iwai; M Sakai; M Muramatsu; Y Ito
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

5.  Specific transcription factors stimulate simian virus 40 and polyomavirus origins of DNA replication.

Authors:  Z S Guo; M L DePamphilis
Journal:  Mol Cell Biol       Date:  1992-06       Impact factor: 4.272

Review 6.  RNA processing in the polyoma virus life cycle.

Authors:  Yingqun Huang; Gordon G Carmichael
Journal:  Front Biosci (Landmark Ed)       Date:  2009-06-01
  6 in total

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