Literature DB >> 23891561

Competition between pre-mRNAs for the splicing machinery drives global regulation of splicing.

Elizabeth M Munding1, Lily Shiue, Sol Katzman, John Paul Donohue, Manuel Ares.   

Abstract

During meiosis in yeast, global splicing efficiency increases and then decreases. Here we provide evidence that splicing improves due to reduced competition for the splicing machinery. The timing of this regulation corresponds to repression and reactivation of ribosomal protein genes (RPGs) during meiosis. In vegetative cells, RPG repression by rapamycin treatment also increases splicing efficiency. Downregulation of the RPG-dedicated transcription factor gene IFH1 genetically suppresses two spliceosome mutations, prp11-1 and prp4-1, and globally restores splicing efficiency in prp4-1 cells. We conclude that the splicing apparatus is limiting and that pre-messenger RNAs compete. Splicing efficiency of a pre-mRNA therefore depends not just on its own concentration and affinity for limiting splicing factor(s), but also on those of competing pre-mRNAs. Competition between RNAs for limiting processing factors appears to be a general condition in eukaryotes for a variety of posttranscriptional control mechanisms including microRNA (miRNA) repression, polyadenylation, and splicing.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23891561      PMCID: PMC3771316          DOI: 10.1016/j.molcel.2013.06.012

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  92 in total

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Journal:  Cell       Date:  2011-09-15       Impact factor: 41.582

5.  The TOR signaling cascade regulates gene expression in response to nutrients.

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  59 in total

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Review 6.  Therapeutic approaches to treat human spliceosomal diseases.

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Review 7.  Context-dependent control of alternative splicing by RNA-binding proteins.

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8.  The Fission Yeast Pre-mRNA-processing Factor 18 (prp18+) Has Intron-specific Splicing Functions with Links to G1-S Cell Cycle Progression.

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Review 9.  Modulating splicing with small molecular inhibitors of the spliceosome.

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