Understanding the molecular principles governing mRNP architecture

HORIZON.1.1HORIZON-ERCID: 101054447
EC Contribution
€21,713
Consortium Size
1 orgs
Summary

Eukaryotic messenger ribonucleoprotein (mRNP) particles are the functional entities that carry genetic information to the protein synthesizing machinery. These ribonucleoprotein complexes are dynamic and diverse, as highlighted by the copious number of proteins and transcripts identified in global proteomic and transcriptomic studies. However, little is known about the composition and architecture of individual mRNPs, and how changes in mRNP structure relate to their function or to dysfunction. The GOVERNA project will address this gap in knowledge by purifying specific mRNPs and delving into their molecular and structural arrangement. With our preliminary data serving as a springboard, the project combines genomic tagging engineered to maintain the most physiologically relevant conditions, biochemical methods developed to preserve the integrity of transient ribonucleoprotein assemblies, and mass spectrometry and cryo-electron microscopy to identify the composition and architecture of mRNPs. We will zoom-in on a set of paradigms in RNA biology that not only sample the breadth of mRNP diversity, but are also powerful model systems for linking structural information and biological function. We will investigate the molecular features in the three-dimensional organization of nuclear mRNPs from S. cerevisiae and of translationally repressed mRNPs in early developmental stages in D. melanogaster and X. laevis. For mRNPs undergoing active translation, we will investigate the transitions of human beta-globin mRNPs in the course of a surveillance process connected to disease. By studying these examples, we will glean fundamental insights into global principles governing the packaging of mRNPs and the remodeling of their three-dimensional features throughout a transcript’s life-cycle. The cumulative output will illuminate a central node of eukaryotic gene expression that is also particularly timely and relevant given recent developments in mRNA-based therapeutics.

Consortium (1)

Project Results (8)

Source: CORDIS, the EU research results database.

Publications (6)
Molecular basis of human polyA polymerase recruitment by mPSF
RNA: A Publication of the RNA Society· 2024DOI
Todesca, S., Sandmeir, F., Keidel, A., & Conti, E.
Structural basis of mRNA decay by the human exosome-ribosome supercomplex
Nature· 2024DOI
Alexander Kögel, Achim Keidel, Matina-Jasemi Loukeri Christopher C. Kuhn, Lukas M. Langer, Ingmar B. Schäfer and Elena Conti
UPF1 helicase orchestrates mutually exclusive interactions with the SMG6 endonuclease and UPF2
Nucleic Acids Research· 2024DOI
Lukas M. Langer, Katharina Kurscheidt, Jérôme Basquin, Fabien Bonneau, Iuliia Iermak, Claire Basquin, and Elena Conti
Molecular Cell
Molecular Cell· 2023DOI
Achim Keidel, Alexander Kögel, Peter Reichelt, Eva Kowalinski, Ingmar B. Schäfer, Elena Conti
Nuclear mRNPs are compact particles packaged with a network of proteins promoting RNA–RNA interactions
Genes & Development· 2023DOI
Fabien Bonneau; Jérôme Basquin; Barbara Steigenberger; Tillman Schäfer; Ingmar B. Schäfer; Elena Conti
The human CNOT1-CNOT10-CNOT11 complex forms a structural platform for protein-protein interactions
Cell Reports· 2023DOI
Fabienne Mauxion, Jérôme Basquin, Sevim Ozgur, Marion Rame, Jana Albrecht, Ingmar Schäfer, Bertrand Séraphin, Elena Conti
Deliverables (1)
Data Management Plan
Other Results (1)
Periodic Reporting for period 1 - GOVERNA (Understanding the molecular principles governing mRNP architecture)