Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

Mechanistic investigation of the cross-talk between spliceosomal complexes and polyadenylation factors

In plain English

AI plain-English summary

Every time a cell reads a gene, it must cut and stitch the genetic message before it can be used — and two massive protein machines, the spliceosome and the polyadenylation apparatus, physically lock together to coordinate this editing. Despite decades of study, no one has seen exactly how these two machines interact. The spliceosome contains over 70 proteins, the polyadenylation apparatus more than 20, and their combined assembly is so large, complex, and fleeting that conventional methods cannot capture it. This leaves a fundamental gap in understanding how cells regulate which parts of a gene become part of the final message — and which are discarded. The researchers will use cryo-electron microscopy to freeze these assemblies mid-action and determine their three-dimensional structures. If successful, this will reveal the mechanical handshake between splicing and polyadenylation, showing how the cell prevents errors like premature gene truncation. This is fundamental science. There is no immediate practical application. But the machinery of gene expression underpins every living cell, and past structural discoveries — from the ribosome to CRISPR enzymes — have repeatedly opened doors to new medicines and biotechnologies. A mechanistic map of this cross-talk could, in time, inform therapies for genetic disorders where splicing or polyadenylation goes wrong.

View original technical description
Splicing and polyadenylation are two essential steps of gene expression that account, to a great extent, for the complexity of eukaryotes. The two processes are catalysed by the spliceosome and the polyadenylation apparatus – two macromolecular machines of megadalton-size which contain more than 70 and 20 proteins, respectively. The two machines associate physically to form composite assemblies, where cross-talk events support emerging layers of regulation of splicing and polyadenylation. These assemblies are primarily unexplored from a mechanistic perspective, due to their excessive size, complexity and dynamics. By employing state of the art technologies and our long-standing expertise in the structural biology of splicing, the time is now ripe for a thoroughgoing investigation of these assemblies. Thus, we aim to stall and isolate composite assemblies relevant for: (i) the coupling between splicing and polyadenylation, (ii) the definition of exons during constitutive and alternative splicing and (iii) protection of genes from premature polyadenylation. Afterwards, we will characterise their 3D structures and functions by electron cryo-microscopy and complementary biochemical methods. The proposed research is expected to be eye-opening and bring a substantive contribution to our understanding of how fundamental processes of gene expression integrate mechanistically.

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Researchers

Vlad Pena (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Unravelling key cellular machinery for spliceosome regulation
CryoEM studies of the spliceosome
The polyA machinery: Elucidating the molecular mechanisms of mRNA polyadenylation, deadenylation and RNA recognition
Biochemical and CryoEM studies of spliceosome activation.
Structural investigation of Sam68-driven transcription/splicing coupling

Original classification

Investigator Award in Science

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