| Literature DB >> 32285620 |
Richard Rigo1, Jérémie Bazin1, Natali Romero-Barrios1, Michaël Moison1,2, Leandro Lucero2, Aurélie Christ1, Moussa Benhamed1, Thomas Blein1, Stéphanie Huguet1, Céline Charon1, Martin Crespi1, Federico Ariel2.
Abstract
Alternative splicing (AS) is a major source of transcriptome diversity. Long noncoding RNAs (lncRNAs) have emerged as regulators of AS through different molecular mechanisms. In Arabidopsis thaliana, the AS regulators NSRs interact with the ALTERNATIVE SPLICING COMPETITOR (ASCO) lncRNA. Here, we analyze the effect of the knock-down and overexpression of ASCO at the genome-wide level and find a large number of deregulated and differentially spliced genes related to flagellin responses and biotic stress. In agreement, ASCO-silenced plants are more sensitive to flagellin. However, only a minor subset of deregulated genes overlaps with the AS defects of the nsra/b double mutant, suggesting an alternative way of action for ASCO. Using biotin-labeled oligonucleotides for RNA-mediated ribonucleoprotein purification, we show that ASCO binds to the highly conserved spliceosome component PRP8a. ASCO overaccumulation impairs the recognition of specific flagellin-related transcripts by PRP8a. We further show that ASCO also binds to another spliceosome component, SmD1b, indicating that it interacts with multiple splicing factors. Hence, lncRNAs may integrate a dynamic network including spliceosome core proteins, to modulate transcriptome reprogramming in eukaryotes.Entities:
Keywords: PRP8a; SmD1b; core splicing factors; flagellin; long noncoding RNA
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Year: 2020 PMID: 32285620 PMCID: PMC7202219 DOI: 10.15252/embr.201948977
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807