Sep 14, 2015

RNA polymerase errors cause splicing defects and can be regulated by differential expression of RNA polymerase subunits

BioRxiv : the Preprint Server for Biology
Lucas B Carey


Errors during transcription may play an important role in determining cellular phenotypes: the RNA polymerase error rate is >4 orders of magnitude higher than that of DNA polymerase and errors are amplified >1000-fold due to translation. However, current methods to measure RNA polymerase fidelity are low-throughout, technically challenging, and organism specific. Here we show that changes in RNA polymerase fidelity can be measured using standard RNA sequencing protocols. We find that RNA polymerase is error-prone, and these errors can result in splicing defects. Furthermore, we find that differential expression of RNA polymerase subunits causes changes in RNA polymerase fidelity, and that coding sequences may have evolved to minimize the effect of these errors. These results suggest that errors cause by RNA polymerase may be a major source of stochastic variability at the level of single cells.

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Mentioned in this Paper

DNA-Directed RNA Polymerase
Sequence Determinations, RNA
RNA Polymerase Assembly Pathway
Transcription, Genetic
Protein Biosynthesis
Nuclear mRNA Cis Splicing, via Spliceosome
RNA polymerase alpha subunit
RNA Splicing
DNA-Directed DNA Polymerase

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