» Articles » PMID: 36797247

Mechanisms of the RNA Helicases DDX42 and DDX46 in Human U2 SnRNP Assembly

Overview
Journal Nat Commun
Specialty Biology
Date 2023 Feb 16
PMID 36797247
Authors
Affiliations
Soon will be listed here.
Abstract

Three RNA helicases - DDX42, DDX46 and DHX15 - are found to be associated with human U2 snRNP, but their roles and mechanisms in U2 snRNP and spliceosome assembly are insufficiently understood. Here we report the cryo-electron microscopy (cryo-EM) structures of the DDX42-SF3b complex and a putative assembly precursor of 17S U2 snRNP that contains DDX42 (DDX42-U2 complex). DDX42 is anchored on SF3B1 through N-terminal sequences, with its N-plug occupying the RNA path of SF3B1. The binding mode of DDX42 to SF3B1 is in striking analogy to that of DDX46. In the DDX42-U2 complex, the N-terminus of DDX42 remains anchored on SF3B1, but the helicase domain has been displaced by U2 snRNA and TAT-SF1. Through in vitro assays, we show DDX42 and DDX46 are mutually exclusive in terms of binding to SF3b. Cancer-driving mutations of SF3B1 target the residues in the RNA path that directly interact with DDX42 and DDX46. These findings reveal the distinct roles of DDX42 and DDX46 in assembly of 17S U2 snRNP and provide insights into the mechanisms of SF3B1 cancer mutations.

Citing Articles

SUGP1 loss is the sole driver of SF3B1 hotspot mutant missplicing in cancer.

Xing P, Bak-Gordon P, Xie J, Zhang J, Liu Z, Manley J bioRxiv. 2025; .

PMID: 40027711 PMC: 11870612. DOI: 10.1101/2025.02.17.638713.


m6A eraser ALKBH5/treRNA1/DDX46 axis regulates BCR expression.

Kapadia B, Roychowdhury A, Kayastha F, Lee W, Nanaji N, Windle J Neoplasia. 2025; 62:101144.

PMID: 39987653 PMC: 11905846. DOI: 10.1016/j.neo.2025.101144.


DHX9 helicase impacts on splicing decisions by modulating U2 snRNP recruitment in Ewing sarcoma cells.

Frezza V, Chellini L, Riccioni V, Bonvissuto D, Palombo R, Paronetto M Nucleic Acids Res. 2025; 53(4).

PMID: 39950342 PMC: 11826090. DOI: 10.1093/nar/gkaf068.


SF3B1: from core splicing factor to oncogenic driver.

Bak-Gordon P, Manley J RNA. 2025; 31(3):314-332.

PMID: 39773890 PMC: 11874996. DOI: 10.1261/rna.080368.124.


SF3B1 thermostability as an assay for splicing inhibitor interactions.

Amorello A, Chandrashekar Reddy G, Melillo B, Cravatt B, Ghosh A, Jurica M J Biol Chem. 2024; 301(2):108135.

PMID: 39725033 PMC: 11791315. DOI: 10.1016/j.jbc.2024.108135.


References
1.
Plaschka C, Newman A, Nagai K . Structural Basis of Nuclear pre-mRNA Splicing: Lessons from Yeast. Cold Spring Harb Perspect Biol. 2019; 11(5). PMC: 6496352. DOI: 10.1101/cshperspect.a032391. View

2.
Kastner B, Fischer N, Golas M, Sander B, Dube P, Boehringer D . GraFix: sample preparation for single-particle electron cryomicroscopy. Nat Methods. 2007; 5(1):53-5. DOI: 10.1038/nmeth1139. View

3.
Zhao B, Li Z, Qian R, Liu G, Fan M, Liang Z . Cancer-associated mutations in SF3B1 disrupt the interaction between SF3B1 and DDX42. J Biochem. 2022; 172(2):117-126. DOI: 10.1093/jb/mvac049. View

4.
Davis I, Leaver-Fay A, Chen V, Block J, Kapral G, Wang X . MolProbity: all-atom contacts and structure validation for proteins and nucleic acids. Nucleic Acids Res. 2007; 35(Web Server issue):W375-83. PMC: 1933162. DOI: 10.1093/nar/gkm216. View

5.
Zhang X, Yan C, Zhan X, Li L, Lei J, Shi Y . Structure of the human activated spliceosome in three conformational states. Cell Res. 2018; 28(3):307-322. PMC: 5835773. DOI: 10.1038/cr.2018.14. View