6ASO

Structure of yeast U6 snRNP with 3'-phosphate terminated U6 RNA

Summary for 6ASO

• Entry DOI: 10.2210/pdb6aso/pdb
• Related: 5VSU
• Descriptor: U4/U6 snRNA-associated-splicing factor PRP24, POTASSIUM ION, MANGANESE (II) ION, ... (13 entities in total)
• Functional Keywords: lsm2-8 spliceosome u6 prp24, splicing
• Biological source: Saccharomyces cerevisiae (Baker's yeast); More
• Total number of polymer chains: 9
• Total formula weight: 155378.61

Authors

Montemayor, E.J.,Brow, D.A.,Butcher, S.E. (deposition date: 2017-08-25, release date: 2018-05-09, Last modification date: 2023-10-04)

Primary citation

Montemayor, E.J.,Didychuk, A.L.,Yake, A.D.,Sidhu, G.K.,Brow, D.A.,Butcher, S.E.
Architecture of the U6 snRNP reveals specific recognition of 3'-end processed U6 snRNA.
Nat Commun, 9:1749-1749, 2018

PubMed Abstract: The spliceosome removes introns from precursor messenger RNA (pre-mRNA) to produce mature mRNA. Prior to catalysis, spliceosomes are assembled de novo onto pre-mRNA substrates. During this assembly process, U6 small nuclear RNA (snRNA) undergoes extensive structural remodeling. The early stages of this remodeling process are chaperoned by U6 snRNP proteins Prp24 and the Lsm2-8 heteroheptameric ring. We now report a structure of the U6 snRNP from Saccharomyces cerevisiae. The structure reveals protein-protein contacts that position Lsm2-8 in close proximity to the chaperone "active site" of Prp24. The structure also shows how the Lsm2-8 ring specifically recognizes U6 snRNA that has been post-transcriptionally modified at its 3' end, thereby elucidating the mechanism by which U6 snRNPs selectively recruit 3' end-processed U6 snRNA into spliceosomes. Additionally, the structure reveals unanticipated homology between the C-terminal regions of Lsm8 and the cytoplasmic Lsm1 protein involved in mRNA decay.

PubMed: 29717126
DOI: 10.1038/s41467-018-04145-4

Experimental method

X-RAY DIFFRACTION (2.71 Å)