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The influence of an alternate template conformation on elongating phage T7 RNA polymerase
Author(s) -
Peter Dröge,
Fritz M. Pohl
Publication year - 1991
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/19.19.5301
Subject(s) - biology , polymerase , transcription bubble , rna polymerase , transcription (linguistics) , microbiology and biotechnology , dna clamp , dna supercoil , dna polymerase , t7 rna polymerase , rna polymerase ii , dna , dna polymerase ii , rna dependent rna polymerase , rna polymerase i , transcription factor ii d , rna , termination factor , bacteriophage , dna replication , promoter , genetics , reverse transcriptase , gene , gene expression , escherichia coli , linguistics , philosophy
We investigated the effect of left-handed Z-DNA on transcription by bacteriophage T7 RNA polymerase in vitro and, surprisingly, found that the enzyme can efficiently utilize a template containing a stretch of left-handed DNA close to the promoter. Analysis of transcription products revealed that only a small fraction of elongating polymerases abort transcription either at the promoter proximal or at the distal B-to-Z junction and, even less frequently, within the stretch of left-handed DNA. Our results indicate that, unlike E. coli RNA polymerase, T7 RNA polymerase can utilize a template with a CG stretch in an alternate conformation. In contrast, polymerases are completely blocked at the promoter proximal junction by a monoclonal antibody directed against Z-DNA. This blockage remains stable over a remarkable time, even when negative supercoiling is released by linearization of the template. Together with our recent finding of transcription-induced formation of Z-DNA (3), our data provide an example for a possible auto-regulatory mechanism that employs a change in DNA conformation.

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