کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1997181 | 1065546 | 2010 | 12 صفحه PDF | دانلود رایگان |

SummaryU2 snRNA-intron branchpoint pairing is a critical step in pre-mRNA recognition by the splicing apparatus, but the mechanism by which these two RNAs engage each other is unknown. Here, we identify a U2 snRNA structure, the branchpoint-interacting stem loop (BSL), which presents the U2 nucleotides that will contact the intron. We provide evidence that the BSL forms prior to interaction with the intron and is disrupted by the DExD/H protein Prp5p during engagement of the snRNA with the intron. In vitro splicing complex assembly in a BSL-destabilized mutant extract suggests that the BSL is required at a previously unrecognized step between commitment complex and prespliceosome formation. The extreme evolutionary conservation of the BSL suggests that it represents an ancient structural solution to the problem of intron branchpoint recognition by dynamic RNA elements that must serve multiple functions at other times during splicing.
► Mutation of invariant U2 residues suppresses a lethal truncation of Prp5p
► The mutations identify a stem loop (BSL) that interacts with the intron branchpoint
► A disrupted BSL perturbs spliceosome assembly in vitro during intron recognition
► A hyperstabilized BSL improves recognition of mutant introns with weak branchpoints
Journal: - Volume 38, Issue 3, 14 May 2010, Pages 416–427