6SNJ
Solution structure of the FUS/TLS RNA recognition motif in complex with U1 snRNA stem loop III
Summary for 6SNJ
Entry DOI | 10.2210/pdb6snj/pdb |
NMR Information | BMRB: 34427 |
Descriptor | RNA-binding protein FUS, U1 snRNA stem loop III, RNA (28-MER) (2 entities in total) |
Functional Keywords | splicing regulation, fus-u1snrnp, spliceosome, splicing |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 2 |
Total formula weight | 23091.82 |
Authors | Campagne, S.,Allain, F.H. (deposition date: 2019-08-26, release date: 2020-10-28, Last modification date: 2024-06-19) |
Primary citation | Jutzi, D.,Campagne, S.,Schmidt, R.,Reber, S.,Mechtersheimer, J.,Gypas, F.,Schweingruber, C.,Colombo, M.,von Schroetter, C.,Loughlin, F.E.,Devoy, A.,Hedlund, E.,Zavolan, M.,Allain, F.H.,Ruepp, M.D. Aberrant interaction of FUS with the U1 snRNA provides a molecular mechanism of FUS induced amyotrophic lateral sclerosis. Nat Commun, 11:6341-6341, 2020 Cited by PubMed Abstract: Mutations in the RNA-binding protein Fused in Sarcoma (FUS) cause early-onset amyotrophic lateral sclerosis (ALS). However, a detailed understanding of central RNA targets of FUS and their implications for disease remain elusive. Here, we use a unique blend of crosslinking and immunoprecipitation (CLIP) and NMR spectroscopy to identify and characterise physiological and pathological RNA targets of FUS. We find that U1 snRNA is the primary RNA target of FUS via its interaction with stem-loop 3 and provide atomic details of this RNA-mediated mode of interaction with the U1 snRNP. Furthermore, we show that ALS-associated FUS aberrantly contacts U1 snRNA at the Sm site with its zinc finger and traps snRNP biogenesis intermediates in human and murine motor neurons. Altogether, we present molecular insights into a FUS toxic gain-of-function involving direct and aberrant RNA-binding and strengthen the link between two motor neuron diseases, ALS and spinal muscular atrophy (SMA). PubMed: 33311468DOI: 10.1038/s41467-020-20191-3 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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