生物
RNA剪接
内含子
RNA聚合酶Ⅱ
拼接因子
遗传学
抄写(语言学)
外显子剪接增强剂
SR蛋白
细胞生物学
核糖核酸
基因
基因表达
发起人
语言学
哲学
作者
Vahid Aslanzadeh,Yuanhua Huang,Guido Sanguinetti,Jean D. Beggs
出处
期刊:Genome Research
[Cold Spring Harbor Laboratory Press]
日期:2017-12-18
卷期号:28 (2): 203-213
被引量:116
标识
DOI:10.1101/gr.225615.117
摘要
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.
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