Alternative splicing and evolution: diversification, exon definition and function
By Hadas Keren, Galit Lev-Maor, Gil Ast. 2010
1,057 citations recorded by the source corpus.
Subfields: Molecular Biology
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In Molecular Biology
- Christophe Dessimoz
- Natasha M. Glover
- David Moi
- Adrian M. Altenhoff
- T. Cooper
- Benjamin J. Blencowe
- Alex Warwick Vesztrocy
- Andrea Barta
Citations in the corpus
- OMA orthology in 2021: website overhaul, conserved isoforms, ancestral gene order and more (2020, background): “Eukaryotic species, especially vertebrates, use alternative splicing, by which a diversity of protein sequences can originate from a single gene by varying combinations of its exons (9).”
- Pol III binding in six mammalian genomes shows high conservation among amino acid isotypes, despite divergence in tRNA gene usage (2011, neutral): “RNA polymerase II (pol II), which is responsible for protein-coding mRNA synthesis, has been well-characterized to bind in vivo to many regions not actively transcribed due to stalled polymerase activity 19,20 , alternate transcription start sites 21 , and regulated alternative splicing 22 .”
- rMATS: Robust and flexible detection of differential alternative splicing from replicate RNA-Seq data (2014, background): “RNA sequencing | alternative splicing | exon | isoform | transcriptome A lternative splicing generates tremendous transcriptomic and proteomic complexity in higher eukaryotes (1 – 4).”
- A census of human RNA-binding proteins (2014, positive): “alternative splicing and polyadenylation) (Chen and Manley, 2009; Keren et al., 2010).”
- Divergence of duplicate genes in exon–intron structure (2012, background): “Second, alternative splicing does not necessarily need the mutation or modification of the genomic sequences, whereas exonization/pseudoexonization requires the creation and/or fixation of a novel start/stop codon (of a gene) or donor/acceptor site (of an intron) (13, 22, 23).”
- Alternative Splicing Regulatory Networks: Functions, Mechanisms, and Evolution. (2019, background): “Intronic sequences derived from transposable elements (TEs) are also a particularly common source of cis-acting elements that vary across evolution and can regulate splicing (Gal-Mark et al., 2009; Keren et al., 2010) (Figure 5a).”
- Mechanisms and Functions of Long Non-Coding RNAs at Multiple Regulatory Levels (2019, background): “Most of the genes (~95%) in human cells are selectively spliced [54].”
- Complexity of the Alternative Splicing Landscape in Plants[C][W][OPEN] (2013, background): “Analysis of the large pool of newly discovered U12-type introns might change this number (Zhu and Brendel, 2003; Basu et al., 2008).”
- MATS: a Bayesian framework for flexible detection of differential alternative splicing from RNA-Seq data (2012, background): “Alternative splicing plays critical roles in regulating gene function and activity in higher eukaryotes (1).”
- Functional consequences of developmentally regulated alternative splicing (2011, background): “It is likely that a large fraction of mRNA diversity has no detectable function within an organism, although some of it provides fodder for the derivation of functional splice variants on an evolutionary timescal”