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A Cre Transcription Fidelity Reporter Identifies GreA as a Major RNA Proofreading Factor in Escherichia coli

We made a coupled genetic reporter that detects rare transcription misincorporation errors to measure RNA polymerase transcription fidelity in Escherichia coli. Using this reporter, we demonstrated in vivo that the transcript cleavage factor GreA, but not GreB, is essential for proofreading of a tra...

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Detalles Bibliográficos
Autores principales: Bubunenko, Mikhail G., Court, Carolyn B., Rattray, Alison J., Gotte, Deanna R., Kireeva, Maria L., Irizarry-Caro, Jorge A., Li, Xintian, Jin, Ding J., Court, Donald L., Strathern, Jeffrey N., Kashlev, Mikhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419468/
https://www.ncbi.nlm.nih.gov/pubmed/28341651
http://dx.doi.org/10.1534/genetics.116.198960
Descripción
Sumario:We made a coupled genetic reporter that detects rare transcription misincorporation errors to measure RNA polymerase transcription fidelity in Escherichia coli. Using this reporter, we demonstrated in vivo that the transcript cleavage factor GreA, but not GreB, is essential for proofreading of a transcription error where a riboA has been misincorporated instead of a riboG. A greA mutant strain had more than a 100-fold increase in transcription errors relative to wild-type or a greB mutant. However, overexpression of GreB in ΔgreA cells reduced the misincorporation errors to wild-type levels, demonstrating that GreB at high concentration could substitute for GreA in RNA proofreading activity in vivo.