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• W2895243510 startingPage "10598" @default.
• W2895243510 abstract "The spliceosome catalyzes the removal of introns from pre-messenger RNA (mRNA) and subsequent pairing of exons with remarkable fidelity. Some exons are known to be skipped or included in the mature mRNA in a cell type- or context-dependent manner (cassette exons), thereby contributing to the diversification of the human proteome. Interestingly, splicing is initiated (and sometimes completed) co-transcriptionally. Here, we develop a kinetic mathematical modeling framework to investigate alternative co-transcriptional splicing (CTS) and, specifically, the control of cassette exons’ inclusion. We show that when splicing is co-transcriptional, default splice patterns of exon inclusion are more likely than when splicing is post-transcriptional, and that certain exons are more likely to be regulatable (i.e. cassette exons) than others, based on the exon–intron structure context. For such regulatable exons, transcriptional elongation rates may affect splicing outcomes. Within the CTS paradigm, we examine previously described hypotheses of co-operativity between splice sites of short introns (i.e. ‘intron definition’) or across short exons (i.e. ‘exon definition’), and find that models encoding these faithfully recapitulate observations in the fly and human genomes, respectively." @default.
• W2895243510 created "2018-10-12" @default.
• W2895243510 creator A5028031580 @default.
• W2895243510 creator A5047177237 @default.
• W2895243510 creator A5076969415 @default.
• W2895243510 date "2018-10-01" @default.
• W2895243510 modified "2023-10-14" @default.
• W2895243510 title "Mathematical modeling identifies potential gene structure determinants of co-transcriptional control of alternative pre-mRNA splicing" @default.
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• W2895243510 doi "https://doi.org/10.1093/nar/gky870" @default.
• W2895243510 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6379712" @default.
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• W2895243510 hasPublicationYear "2018" @default.
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