| Literature DB >> 28739803 |
Agape M Awad1,2, Srivats Venkataramanan2,3, Anish Nag1,2, Anoop Raj Galivanche3, Michelle C Bradley1,2, Lauren T Neves2,3, Stephen Douglass3, Catherine F Clarke4,2, Tracy L Johnson5,3.
Abstract
Despite its relatively streamlined genome, there are many important examples of regulated RNA splicing in Saccharomyces cerevisiae Here, we report a role for the chromatin remodeler SWI/SNF in respiration, partially via the regulation of splicing. We find that a nutrient-dependent decrease in Snf2 leads to an increase in splicing of the PTC7 transcript. The spliced PTC7 transcript encodes a mitochondrial phosphatase regulator of biosynthesis of coenzyme Q6 (ubiquinone or CoQ6) and a mitochondrial redox-active lipid essential for electron and proton transport in respiration. Increased splicing of PTC7 increases CoQ6 levels. The increase in PTC7 splicing occurs at least in part due to down-regulation of ribosomal protein gene expression, leading to the redistribution of spliceosomes from this abundant class of intron-containing RNAs to otherwise poorly spliced transcripts. In contrast, a protein encoded by the nonspliced isoform of PTC7 represses CoQ6 biosynthesis. Taken together, these findings uncover a link between Snf2 expression and the splicing of PTC7 and establish a previously unknown role for the SWI/SNF complex in the transition of yeast cells from fermentative to respiratory modes of metabolism.Entities:
Keywords: Saccharomyces cerevisiae; alternative splicing; chromatin remodeling; coenzyme Q; gene expression; lipid metabolism; metabolic regulation; mitochondrial metabolism; phosphorylation
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Year: 2017 PMID: 28739803 PMCID: PMC5592666 DOI: 10.1074/jbc.M117.798397
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157