PaperPlayer biorxiv biophysics

Structural basis for conformational equilibrium of the catalytic spliceosome


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Link to bioRxiv paper:
http://biorxiv.org/cgi/content/short/2020.09.22.306647v1?rss=1
Authors: Wilkinson, M. E., Fica, S. M., Galej, W. P., Nagai, K.
Abstract:
The catalytic spliceosome exists in equilibrium between the branching (B*/C) and exon ligation (C*/P) conformations. Here we present the electron cryo-microscopy reconstruction of the Saccharomyces cerevisiae C-complex spliceosome at 2.8 [A] resolution and identify a novel C-complex intermediate (Ci) that elucidates the molecular basis for this equilibrium. In the Ci conformation, the exon-ligation factors Prp18 and Slu7 are already bound before ATP hydrolysis by Prp16, which destabilises the branching conformation. Biochemical assays suggest these pre-bound factors prime C complex for conversion to C* by Prp16. A complete model of the Prp19-complex (NTC) shows how branching factors Yju2 and Isy1 bind the NTC before branching. Prp16 remodels Yju2 binding after branching, allowing Yju2 to remain associated with the C* complex to promote exon ligation. Our results explain how Prp16 action modulates dynamic binding of step-specific factors to alternatively stabilise the C or C* conformation and establish equilibrium of the catalytic spliceosome.
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