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- W4210548135 abstract "RNA primers for DNA replication are usually synthesized by specialized enzymes, the primases. However, some replication systems have evolved to use cellular DNA-dependent RNA polymerase for primer synthesis. The main requirement for the replication primer, an exposed RNA 3' end annealed to the DNA template, is not compatible with known conformations of the transcription elongation complex, raising a question of how the priming is achieved. Here we show that a previously unrecognized kind of transcription complex is formed during RNA polymerase-catalysed synthesis of the M13 bacteriophage replication primer. The complex contains an overextended RNA-DNA hybrid bound in the RNA-polymerase trough that is normally occupied by downstream double-stranded DNA, thus leaving the 3' end of the RNA available for interaction with DNA polymerase. Transcription complexes with similar topology may prime the replication of other bacterial mobile elements and may regulate transcription elongation under conditions that favour the formation of an extended RNA-DNA hybrid. PMID: 16452982" @default.
- W4210548135 created "2022-02-08" @default.
- W4210548135 creator A5024724276 @default.
- W4210548135 date "2006-03-16" @default.
- W4210548135 modified "2023-09-23" @default.
- W4210548135 title "Faculty Opinions recommendation of The mechanism of DNA replication primer synthesis by RNA polymerase." @default.
- W4210548135 doi "https://doi.org/10.3410/f.1031606.367758" @default.
- W4210548135 hasPublicationYear "2006" @default.
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