2019
DOI: 10.1016/j.tplants.2019.02.006
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Perspective on Alternative Splicing and Proteome Complexity in Plants

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Cited by 109 publications
(98 citation statements)
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“…This shift involves translational control (Juntawong et al , ) and the sequestration and/or degradation of many mRNA species via cytoplasmic organelles (Chantarachot and Bailey‐Serres, ) (P‐bodies and stress bodies, for example). The combination of post‐transcriptional and translation controls serves to effectively and rapidly reprogramme protein biosynthesis in response to stress (Chaudhary et al , ).…”
Section: Discussionmentioning
confidence: 99%
“…This shift involves translational control (Juntawong et al , ) and the sequestration and/or degradation of many mRNA species via cytoplasmic organelles (Chantarachot and Bailey‐Serres, ) (P‐bodies and stress bodies, for example). The combination of post‐transcriptional and translation controls serves to effectively and rapidly reprogramme protein biosynthesis in response to stress (Chaudhary et al , ).…”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, some proteomic studies suggest that AS may not significantly contribute to protein diversity and only single dominant isoforms are represented at the protein level for most of the protein-coding genes (Ezkurdia et al, 2015; Tress et al, 2017a). Apparently, these contradictions stem from the lower depth and limitations of mass spectrometry (MS) techniques to detect changes in protein domains as a result of AS (Wang et al, 2018; Chaudhary et al, 2019). In this review, basic differences in the mechanism of AS and its contribution toward protein diversity in plants and humans are discussed.…”
Section: Introductionmentioning
confidence: 99%
“…The choice of splice sites mainly depends on the recruitment of splicing factors and heterogeneous nuclear ribonucleoproteins (hnRNPs), but other splicing regulators such as SR proteins and KH-domain RBPs are also involved in this process (8,9). In addition to transcripts encoding proteins with different properties, AS leads to the production of transcripts with a premature termination codon (PTC) that marks them for degradation by the nonsense-medicated decay (NMD) mechanism (10)(11)(12). In Arabidopsis, 61% of genes including the components of the circadian oscillator such as morning-phased CIRCADIAN CLOCK ASSOCIATED 1 (CCA1), LATE ELONGATED HYPOCOTYL (LHY), day-phased PSEUDO-RESPONSE REGULATORs (PRRs) and REVEILLE 8 (RVE8), evening-phased TIMING OF CAB EXPRESSION 1 (TOC1), GIGANTEA (GI), EARLY FLOWERING 3 (ELF3) have been shown to be alternatively spliced (13)(14)(15)(16).…”
Section: Introductionmentioning
confidence: 99%