Transcription rate strongly affects splicing fidelity and cotranscriptionality in budding yeast

• Published in: Genome research Vol. 28; no. 2; pp. 203 - 213
• Main Authors: Aslanzadeh, Vahid, Huang, Yuanhua, Sanguinetti, Guido, Beggs, Jean D.
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 01.02.2018
• Subjects: Alternative Splicing; DNA-directed RNA polymerase; Efficiency; Elongation; Exons - genetics; Fidelity; Gene expression; Introns - genetics; Mammalian cells; Protein structure; Proteins; RNA polymerase; RNA Polymerase II - genetics; RNA Splice Sites - genetics; RNA Splicing - genetics; Saccharomycetales - genetics; Secondary structure; Transcription; Transcription Elongation, Genetic; Transcription, Genetic; Yeast
• ISSN: 1088-9051; 1549-5469; 1549-5469
• DOI: 10.1101/gr.225615.117

The functional consequences of alternative splicing on altering the transcription rate have been the subject of intensive study in mammalian cells but less is known about effects of splicing on changing the transcription rate in yeast. We present several lines of evidence showing that slow RNA polymerase II elongation increases both cotranscriptional splicing and splicing efficiency and that faster elongation reduces cotranscriptional splicing and splicing efficiency in budding yeast, suggesting that splicing is more efficient when cotranscriptional. Moreover, we demonstrate that altering the RNA polymerase II elongation rate in either direction compromises splicing fidelity, and we reveal that splicing fidelity depends largely on intron length together with secondary structure and splice site score. These effects are notably stronger for the highly expressed ribosomal protein coding transcripts. We propose that transcription by RNA polymerase II is tuned to optimize the efficiency and accuracy of ribosomal protein gene expression, while allowing flexibility in splice site choice with the nonribosomal protein transcripts.