All-atom simulations disentangle the functional dynamics underlying gene maturation in the intron lariat spliceosome.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 29891649.
- Also identified by DOI 10.1073/pnas.1802963115 and PMC identifier 6042132.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
The spliceosome (SPL) is a majestic macromolecular machinery composed of five small nuclear RNAs and hundreds of proteins. SPL removes noncoding introns from precursor messenger RNAs (pre-mRNAs) and ligates coding exons, giving rise to functional mRNAs. Building on the first SPL structure solved at near-atomic-level resolution, here we elucidate the functional dynamics of the intron lariat spliceosome (ILS) complex through multi-microsecond-long molecular-dynamics simulations of ∼1,000,000 atoms models. The ILS essential dynamics unveils (<i>i</i>) the leading role of the Spp42 protein, which heads the gene maturation by tuning the motions of distinct SPL components, and (<i>ii</i>) the critical participation of the Cwf19 protein in displacing the intron lariat/U2 branch helix. These findings provide unprecedented details on the SPL functional dynamics, thus contributing to move a step forward toward a thorough understanding of eukaryotic pre-mRNA splicing.
Medical subject headings
- Computer Simulation
- Introns
- Models, Genetic
- Nucleic Acid Conformation
- RNA Precursors
- RNA Splicing
- Repressor Proteins
- Ribonucleoprotein, U5 Small Nuclear
- Schizosaccharomyces pombe Proteins
- Spliceosomes