Literature DB >> 2581137

Expression of enhanced levels of small RNA polymerase III transcripts encoded by the B2 repeats in simian virus 40-transformed mouse cells.

K Singh, M Carey, S Saragosti, M Botchan.   

Abstract

Although specific viral genes are known which are sufficient to transform certain types of cells, viral transformation has been shown to be accompanied by a change in the level of expression of cellular genes. Assuming that this latter class of genes is involved in some way in the establishment of the transformed state, we and others have sought to characterize them. To this end, we constructed a complementary DNA library from a simian virus 40 (SV40)-transformed mouse cell line and screened this library for induced genes. Here we focus on the characterization of a specific cDNA clone called 10 lambda 5. We show that the clone 10 lambda 5 contains a B2 repeat, and that the levels of the small heterogeneously sized B2 cytoplasmic RNAs homologous to 10 lambda 5 are enhanced in transformed cells. Our studies show that these RNAs are a specific class of polymerase III transcripts containing a highly conserved 5' end. SV40 transformation results, therefore, in the activation of specific polymerase III transcripts as well as specific polymerase II transcripts.

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Year:  1985        PMID: 2581137     DOI: 10.1038/314553a0

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


  55 in total

1.  K562 cells implicate increased chromatin accessibility in Alu transcriptional activation.

Authors:  T H Li; C Kim; C M Rubin; C W Schmid
Journal:  Nucleic Acids Res       Date:  2000-08-15       Impact factor: 16.971

2.  Stress induction of Bm1 RNA in silkworm larvae: SINEs, an unusual class of stress genes.

Authors:  R H Kimura; P V Choudary; K K Stone; C W Schmid
Journal:  Cell Stress Chaperones       Date:  2001-07       Impact factor: 3.667

Review 3.  RNA polymerase III transcription: its control by tumor suppressors and its deregulation by transforming agents.

Authors:  T R Brown; P H Scott; T Stein; A G Winter; R J White
Journal:  Gene Expr       Date:  2000

4.  A role for the TATA-box-binding protein component of the transcription factor IID complex as a general RNA polymerase III transcription factor.

Authors:  R J White; S P Jackson; P W Rigby
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-01       Impact factor: 11.205

5.  In vitro and in vivo analysis of the c-myc RNA polymerase III promoter.

Authors:  D J Sussman; J Chung; P Leder
Journal:  Nucleic Acids Res       Date:  1991-09-25       Impact factor: 16.971

6.  Transcripts synthesized by RNA polymerase III can be polyadenylated in an AAUAAA-dependent manner.

Authors:  Olga R Borodulina; Dmitri A Kramerov
Journal:  RNA       Date:  2008-07-24       Impact factor: 4.942

7.  Expression of small cytoplasmic transcripts of the rat identifier element in vivo and in cultured cells.

Authors:  R D McKinnon; P Danielson; M A Brow; F E Bloom; J G Sutcliffe
Journal:  Mol Cell Biol       Date:  1987-06       Impact factor: 4.272

8.  Induction of B2 RNA polymerase III transcription by heat shock: enrichment for heat shock induced sequences in rodent cells by hybridization subtraction.

Authors:  A J Fornace; J B Mitchell
Journal:  Nucleic Acids Res       Date:  1986-07-25       Impact factor: 16.971

9.  Activation of RNA polymerase III transcription of human Alu repetitive elements by adenovirus type 5: requirement for the E1b 58-kilodalton protein and the products of E4 open reading frames 3 and 6.

Authors:  B Panning; J R Smiley
Journal:  Mol Cell Biol       Date:  1993-06       Impact factor: 4.272

Review 10.  RNA polymerase III repression by the retinoblastoma tumor suppressor protein.

Authors:  Alison Gjidoda; R William Henry
Journal:  Biochim Biophys Acta       Date:  2012-10-12
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