| Literature DB >> 22000012 |
Julie Parenteau1, Mathieu Durand, Geneviève Morin, Jules Gagnon, Jean-François Lucier, Raymund J Wellinger, Benoit Chabot, Sherif Abou Elela.
Abstract
In budding yeast, the most abundantly spliced pre-mRNAs encode ribosomal proteins (RPs). To investigate the contribution of splicing to ribosome production and function, we systematically eliminated introns from all RP genes to evaluate their impact on RNA expression, pre-rRNA processing, cell growth, and response to stress. The majority of introns were required for optimal cell fitness or growth under stress. Most introns are found in duplicated RP genes, and surprisingly, in the majority of cases, deleting the intron from one gene copy affected the expression of the other in a nonreciprocal manner. Consistently, 70% of all duplicated genes were asymmetrically expressed, and both introns and gene deletions displayed copy-specific phenotypic effects. Together, our results indicate that splicing in yeast RP genes mediates intergene regulation and implicate the expression ratio of duplicated RP genes in modulating ribosome function.Entities:
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Year: 2011 PMID: 22000012 DOI: 10.1016/j.cell.2011.08.044
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582