Literature DB >> 9237994

Preferential interaction of the his pause RNA hairpin with RNA polymerase beta subunit residues 904-950 correlates with strong transcriptional pausing.

D Wang1, K Severinov, R Landick.   

Abstract

RNA secondary structures (hairpins) that form as the nascent RNA emerges from RNA polymerase are important components of many signals that regulate transcription, including some pause sites, all rho-independent terminators, and some antiterminators. At the his leader pause site, a 5-bp-stem, 8-nt-loop pause RNA hairpin forms 11 nt from the RNA 3' end and stabilizes a transcription complex conformation slow to react with NTP substrate. This stabilization appears to depend at least in part on an interaction with RNA polymerase. We tested for RNA hairpin interaction with the paused polymerase by crosslinking 5-iodoUMP positioned specifically in the hairpin loop. In the paused conformation, strong and unusual crosslinking of the pause hairpin to beta904-950 replaced crosslinking to beta' and to other parts of beta that occurred in nonpaused complexes prior to hairpin formation. These changes in nascent RNA interactions may inhibit reactive alignment of the RNA 3' end in the paused complex and be related to events at rho-independent terminators.

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Year:  1997        PMID: 9237994      PMCID: PMC22946          DOI: 10.1073/pnas.94.16.8433

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  43 in total

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Authors:  S W Cheng; E C Lynch; K R Leason; D L Court; B A Shapiro; D I Friedman
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Authors:  J P Richardson
Journal:  Crit Rev Biochem Mol Biol       Date:  1993       Impact factor: 8.250

6.  Prediction of rho-independent Escherichia coli transcription terminators. A statistical analysis of their RNA stem-loop structures.

Authors:  Y d'Aubenton Carafa; E Brody; C Thermes
Journal:  J Mol Biol       Date:  1990-12-20       Impact factor: 5.469

7.  Structure of RNA and DNA chains in paused transcription complexes containing Escherichia coli RNA polymerase.

Authors:  D N Lee; R Landick
Journal:  J Mol Biol       Date:  1992-12-05       Impact factor: 5.469

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Journal:  J Mol Biol       Date:  1992-03-05       Impact factor: 5.469

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  15 in total

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6.  The bacteriophage lambda Q antiterminator protein contacts the beta-flap domain of RNA polymerase.

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8.  Escherichia coli rho factor induces release of yeast RNA polymerase II but not polymerase I or III.

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Review 9.  Control of transcriptional elongation.

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10.  Folding of a large ribozyme during transcription and the effect of the elongation factor NusA.

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