Publications by authors named "Taiyun Wang"

Article Synopsis
  • Lariat RNAs are generated during the splicing of pre-mRNA in eukaryotes, formed from excised introns when specific splice sites join.
  • Typically, lariat RNAs are linearized and degraded by the RNA debranching enzyme 1 (DBR1), but recent advancements in RNA sequencing have shown that many can accumulate stably in both animals and plants.
  • This study focuses on a large-scale analysis to identify lariat RNAs, also known as intronic circular RNAs, in Arabidopsis using RNA-sequencing data.
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Translational repression is a conserved mechanism in microRNA (miRNA)-guided gene silencing. In Arabidopsis, ARGONAUTE1 (AGO1), the major miRNA effector, localizes in the cytoplasm for mRNA cleavage and at the endoplasmic reticulum (ER) for translational repression of target genes. However, the mechanism underlying miRNA-mediated translational repression is poorly understood.

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Lariats are formed by excised introns, when the 5' splice site joins with the branchpoint (BP) during splicing. Although lariat RNAs are usually degraded by RNA debranching enzyme 1, recent findings in animals detected many lariat RNAs under physiological conditions. By contrast, the features of BPs and to what extent lariat RNAs accumulate naturally are largely unexplored in plants.

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Lariat RNA is produced during pre-mRNA splicing, and it is traditionally thought as by-products, due to the quick turnover by debranching followed by degradation. However, recent findings identified many lariat RNAs accumulate with a circular form in higher eukaryotes. Although the remarkable accumulation, biological consequence of lariat-derived circular RNAs (here we name laciRNAs) remains largely unknown.

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