| Literature DB >> 23223234 |
Jeffrey Strathern1, Francisco Malagon, Jordan Irvin, Deanna Gotte, Brenda Shafer, Maria Kireeva, Lucyna Lubkowska, Ding Jun Jin, Mikhail Kashlev.
Abstract
The fidelity of RNA synthesis depends on both accurate template-mediated nucleotide selection and proper maintenance of register between template and RNA. Loss of register, or transcriptional slippage, is particularly likely on homopolymeric runs in the template. Transcriptional slippage can alter the coding capacity of mRNAs and is used as a regulatory mechanism. Here we describe mutations in the largest subunit of Saccharomyces cerevisiae RNA polymerase II that substantially increase the level of transcriptional slippage. Alleles of RPB1 (RPO21) with elevated slippage rates were identified among 6-azauracil-sensitive mutants and were also isolated using a slippage-dependent reporter gene. Biochemical characterization of polymerase II isolated from these mutants confirms elevated levels of transcriptional slippage.Entities:
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Year: 2012 PMID: 23223234 PMCID: PMC3554935 DOI: 10.1074/jbc.M112.429506
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157