Literature DB >> 27240813

Lessons from non-canonical splicing.

Christopher R Sibley1,2, Lorea Blazquez1, Jernej Ule1.   

Abstract

Recent improvements in experimental and computational techniques that are used to study the transcriptome have enabled an unprecedented view of RNA processing, revealing many previously unknown non-canonical splicing events. This includes cryptic events located far from the currently annotated exons and unconventional splicing mechanisms that have important roles in regulating gene expression. These non-canonical splicing events are a major source of newly emerging transcripts during evolution, especially when they involve sequences derived from transposable elements. They are therefore under precise regulation and quality control, which minimizes their potential to disrupt gene expression. We explain how non-canonical splicing can lead to aberrant transcripts that cause many diseases, and also how it can be exploited for new therapeutic strategies.

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Year:  2016        PMID: 27240813      PMCID: PMC5154377          DOI: 10.1038/nrg.2016.46

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  192 in total

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Journal:  Genome Res       Date:  2015-04-16       Impact factor: 9.043

6.  A comprehensive survey of non-canonical splice sites in the human transcriptome.

Authors:  Guillermo E Parada; Roberto Munita; Cledi A Cerda; Katia Gysling
Journal:  Nucleic Acids Res       Date:  2014-08-14       Impact factor: 16.971

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  85 in total

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Review 4.  Deep intronic mutations and human disease.

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Review 5.  Normal and altered pre-mRNA processing in the DMD gene.

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Review 6.  Influence of transcriptional variants on metastasis.

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7.  Alternative RNA Splicing as a Potential Major Source of Untapped Molecular Targets in Precision Oncology and Cancer Disparities.

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8.  Zmat3 Is a Key Splicing Regulator in the p53 Tumor Suppression Program.

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