Lariat sequencing in a unicellular yeast identifies regulated alternative splicing of exons that are evolutionarily conserved with humans

Alternative splicing is a potent regulator of gene expression that vastly increases proteomic diversity in multicellular eukaryotes and is associated with organismal complexity. Although alternative splicing is widespread in vertebrates, little is known about the evolutionary origins of this process...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 110; no. 31; pp. 12762 - 12767
Main Authors Awan, Ali R., Manfredo, Amanda, Pleiss, Jeffrey A.
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 30.07.2013
National Acad Sciences
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Summary:Alternative splicing is a potent regulator of gene expression that vastly increases proteomic diversity in multicellular eukaryotes and is associated with organismal complexity. Although alternative splicing is widespread in vertebrates, little is known about the evolutionary origins of this process, in part because of the absence of phylogenetically conserved events that cross major eukaryotic clades. Here we describe a lariat-sequencing approach, which offers high sensitivity for detecting splicing events, and its application to the unicellular fungus, Schizosaccharomyces pombe , an organism that shares many of the hallmarks of alternative splicing in mammalian systems but for which no previous examples of exon-skipping had been demonstrated. Over 200 previously unannotated splicing events were identified, including examples of regulated alternative splicing. Remarkably, an evolutionary analysis of four of the exons identified here as subject to skipping in S. pombe reveals high sequence conservation and perfect length conservation with their homologs in scores of plants, animals, and fungi. Moreover, alternative splicing of two of these exons have been documented in multiple vertebrate organisms, making these the first demonstrations of identical alternative-splicing patterns in species that are separated by over 1 billion y of evolution.
Bibliography:http://dx.doi.org/10.1073/pnas.1218353110
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Edited by Michael Rosbash, Howard Hughes Medical Institute, Brandeis University, Waltham, MA, and approved June 26, 2013 (received for review October 24, 2012)
Author contributions: A.R.A., A.M., and J.A.P. designed research; A.R.A. and A.M. performed research; A.R.A. contributed new reagents/analytic tools; A.R.A., A.M., and J.A.P. analyzed data; and A.R.A. and J.A.P. wrote the paper.
ISSN:0027-8424
1091-6490
1091-6490
DOI:10.1073/pnas.1218353110