Literature DB >> 8074291

Activation of pausing RNA polymerases by nuclear run-on experiments.

D Eick1, F Kohlhuber, D A Wolf, L J Strobl.   

Abstract

The nuclear run-on transcription assay is the only approach to measure the transcriptional activity of a given gene in its genuine structural and regulatory cellular context. However, serious problems in the interpretation of results can arise from the artificial activation of paused RNA polymerases during the transcription reaction, leading to false results with regard to the level and mode of gene regulation in vivo. We have used the example of the human proto-oncogene c-myc, which has previously been reported to be regulated by premature termination of transcription, to describe the problems and pitfalls in the interpretation of nuclear run-on experiments. We show here that activation of paused, elongation-incompetent polymerases in nuclear run-on experiments produces a strong transcription signal on c-myc exon 1 in cells which do not express c-myc steady-state RNA.

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Year:  1994        PMID: 8074291     DOI: 10.1006/abio.1994.1190

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  16 in total

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4.  In vivo interpretation of in vitro effect studies with a detailed analysis of the method of in vitro transcription in isolated cell nuclei.

Authors:  R Strand; R Fjelland; T Flatmark
Journal:  Acta Biotheor       Date:  1996-03       Impact factor: 1.774

5.  DNA methylation inhibits elongation but not initiation of transcription in Neurospora crassa.

Authors:  M R Rountree; E U Selker
Journal:  Genes Dev       Date:  1997-09-15       Impact factor: 11.361

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Authors:  Daniel P Morris; Gregory A Michelotti; Debra A Schwinn
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7.  Variable pause positions of RNA polymerase II lie proximal to the c-myc promoter irrespective of transcriptional activity.

Authors:  D A Wolf; L J Strobl; A Pullner; D Eick
Journal:  Nucleic Acids Res       Date:  1995-09-11       Impact factor: 16.971

8.  RNAPol-ChIP: a novel application of chromatin immunoprecipitation to the analysis of real-time gene transcription.

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9.  An exceptionally conserved transcriptional repressor, CTCF, employs different combinations of zinc fingers to bind diverged promoter sequences of avian and mammalian c-myc oncogenes.

Authors:  G N Filippova; S Fagerlie; E M Klenova; C Myers; Y Dehner; G Goodwin; P E Neiman; S J Collins; V V Lobanenkov
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10.  The two steps of poly(A)-dependent termination, pausing and release, can be uncoupled by truncation of the RNA polymerase II carboxyl-terminal repeat domain.

Authors:  Noh Jin Park; David C Tsao; Harold G Martinson
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

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