Fail-Safe Transcriptional Termination for Protein-Coding Genes in S. cerevisiae

Autor: Junya Kawauchi, Nick J. Proudfoot, Hannah E. Mischo, Ana G. Rondón
Rok vydání: 2009
Předmět:
Ribonuclease III
RNA Helicases/genetics
Transcription
Genetic

RNA Stability
RNA-binding protein
RNA polymerase II
Binding Sites/genetics
Terminator Regions
Genetic/physiology

Transcription (biology)
RNA Stability/physiology
DNA/metabolism
Exoribonucleases/genetics
3' Flanking Region
Phosphorylation
Polymerase
Saccharomyces cerevisiae/physiology
Terminator Regions
Genetic

Genetics
Acyltransferases/genetics
Plasmids/genetics
0303 health sciences
Phosphorylation/physiology
030302 biochemistry & molecular biology
Nuclear Proteins
RNA-Binding Proteins
Protein Binding/physiology
Cell biology
Saccharomyces cerevisiae Proteins/genetics
RNA Polymerase II
3' Flanking Region/physiology
RNA Helicases
Plasmids
Protein Binding
Saccharomyces cerevisiae Proteins
Mutation/genetics
PROTEINS
Termination factor
Ribonuclease III/physiology
Saccharomyces cerevisiae
Biology
Article
03 medical and health sciences
RNA
Messenger

Molecular Biology
Gene
030304 developmental biology
Messenger RNA
Binding Sites
DNA Helicases/genetics
DNA Helicases
DNA
Cell Biology
RNA
Messenger/biosynthesis

RNA-Binding Proteins/genetics
Nuclear Proteins/genetics
Antitermination
Exoribonucleases
Mutation
biology.protein
RNA
Transcription
Genetic/physiology

RNA Polymerase II/metabolism
Acyltransferases
Zdroj: Molecular Cell
Rondón, A G, Mischo, H E, Kawauchi, J & Proudfoot, N J 2009, ' Fail-safe transcriptional termination for protein-coding genes in S. cerevisiae ', MOLECULAR CELL, vol. 36, no. 1, pp. 88-98 . https://doi.org/10.1016/j.molcel.2009.07.028
ISSN: 1097-2765
DOI: 10.1016/j.molcel.2009.07.028
Popis: Summary Transcription termination of RNA polymerase II (Pol II) on protein-coding genes in S. cerevisiae relies on pA site recognition by 3′ end processing factors. Here we demonstrate the existence of two alternative termination mechanisms that rescue polymerases failing to disengage from the template at pA sites. One of these fail-safe mechanisms is mediated by the NRD complex, similar to termination of short noncoding genes. The other termination mechanism is mediated by Rnt1 cleavage of the nascent transcript. Both fail-safe termination mechanisms trigger degradation of readthrough transcripts by the exosome. However, Rnt1-mediated termination can also enhance the usage of weak pA signals and thereby generate functional mRNA. We propose that these alternative Pol II termination pathways serve the dual function of avoiding transcription interference and promoting rapid removal of aberrant transcripts.
Databáze: OpenAIRE