Literature DB >> 27923713

When transcription goes on Holliday: Double Holliday junctions block RNA polymerase II transcription in vitro.

Anne Pipathsouk1, Boris P Belotserkovskii1, Philip C Hanawalt2.   

Abstract

Non-canonical DNA structures can obstruct transcription. This transcription blockage could have various biological consequences, including genomic instability and gratuitous transcription-coupled repair. Among potential structures causing transcription blockage are Holliday junctions (HJs), which can be generated as intermediates in homologous recombination or during processing of stalled replication forks. Of particular interest is the double Holliday junction (DHJ), which contains two HJs. Topological considerations impose the constraint that the total number of helical turns in the DNA duplexes between the junctions cannot be altered as long as the flanking DNA duplexes are intact. Thus, the DHJ structure should strongly resist transient unwinding during transcription; consequently, it is predicted to cause significantly stronger blockage than single HJ structures. The patterns of transcription blockage obtained for RNA polymerase II transcription in HeLa cell nuclear extracts were in accordance with this prediction. However, we did not detect transcription blockage with purified T7 phage RNA polymerase; we discuss a possible explanation for this difference. In general, our findings implicate naturally occurring Holliday junctions in transcription arrest.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Genomic instability; Holliday junctions; Repair; Transcription; Unusual DNA structures

Mesh:

Substances:

Year:  2016        PMID: 27923713      PMCID: PMC5315695          DOI: 10.1016/j.bbagrm.2016.12.002

Source DB:  PubMed          Journal:  Biochim Biophys Acta Gene Regul Mech        ISSN: 1874-9399            Impact factor:   4.490


  26 in total

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9.  DNA slip-outs cause RNA polymerase II arrest in vitro: potential implications for genetic instability.

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10.  Transcription blockage by stable H-DNA analogs in vitro.

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  2 in total

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Review 2.  RNA polymerase pausing, stalling and bypass during transcription of damaged DNA: from molecular basis to functional consequences.

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