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Status |
Public on Jun 01, 2024 |
Title |
Structure of an aberrant spliceosome intermediate on its way to disassembly |
Organism |
Schizosaccharomyces pombe |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Intron removal during pre-mRNA splicing is of extraordinary complexity and its disruption causes a vast number of genetic diseases in humans. While key steps of the canonical spliceosome cycle have been revealed by combined structure-function analyses, structural information on an aberrant spliceosome committed to discard is not available. Here, we report the cryo-EM structure of a B state spliceosome intermediate primed for disassembly. We identify the DEAH-box helicase – G patch protein pair (Gih35-Gpl1) to maintain catalytic dormancy with Gpl1 recognizing a remodeled active site of the spliceosome due to a single-nucleotide insertion at the 3’ end of the 5’ exon. Remodeling is communicated to the spliceosome surface and the Ntr1 complex is recruited. Our data pave the way for a targeted analysis of spliceosome-associated quality control.
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Overall design |
Detailed analysis of Ctr1-deficient and WT strains using high throughput poly(A)+ RNA sequencing.
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Contributor(s) |
Horvath A, Fischer T, Soni K |
Citation missing |
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Submission date |
Jun 22, 2023 |
Last update date |
Jun 01, 2024 |
Contact name |
Attila Horvath |
E-mail(s) |
attila.horvath@anu.edu.au
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Organization name |
The Australian National University
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Street address |
Garran Road 131
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City |
Canberra |
State/province |
ACT |
ZIP/Postal code |
2601 |
Country |
Australia |
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Platforms (1) |
GPL28961 |
Illumina NovaSeq 6000 (Schizosaccharomyces pombe) |
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Samples (3) |
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Relations |
BioProject |
PRJNA986513 |