| Literature DB >> 34105434 |
William Martelly1,2, Bernice Fellows1, Paul Kang3, Ajay Vashisht4, James A Wohlschlegel4, Shalini Sharma1.
Abstract
During spliceosome assembly, interactions that bring the 5' and 3' ends of an intron in proximity are critical for the production of mature mRNA. Here, we report synergistic roles for the stem-loops 3 (SL3) and 4 (SL4) of the human U1 small nuclear RNA (snRNA) in maintaining the optimal U1 snRNP function, and formation of cross-intron contact with the U2 snRNP. We find that SL3 and SL4 bind distinct spliceosomal proteins and combining a U1 snRNA activity assay with siRNA-mediated knockdown, we demonstrate that SL3 and SL4 act through the RNA helicase UAP56 and the U2 protein SF3A1, respectively. In vitro analysis using UV crosslinking and splicing assays indicated that SL3 likely promotes the SL4-SF3A1 interaction leading to enhancement of A complex formation and pre-mRNA splicing. Overall, these results highlight the vital role of the distinct contacts of SL3 and SL4 in bridging the pre-mRNA bound U1 and U2 snRNPs during the early steps of human spliceosome assembly.Entities:
Keywords: A complex; DDX39A; DDX39B; E complex; SF3A1; Spliceosome; Stem-loop; U1 snRNA; U1 snRNP; U2 snRNP; UAP56; URH49
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Year: 2021 PMID: 34105434 PMCID: PMC8632089 DOI: 10.1080/15476286.2021.1932360
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.766