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8DGJ

Structural Basis of MicroRNA Biogenesis by Dicer-1 and Its Partner Protein Loqs-PB - complex Ib

Summary for 8DGJ
Entry DOI10.2210/pdb8dgj/pdb
EMDB information27427
DescriptorEndoribonuclease Dcr-1, Loquacious, isoform B (2 entities in total)
Functional Keywordsdicer, dcr-1, loquacious, loqs-pb, mirna, rna binding protein-rna complex, rna binding protein/rna
Biological sourceDrosophila melanogaster (fruit fly)
More
Total number of polymer chains2
Total formula weight305883.66
Authors
Jouravleva, K.,Golovenko, D.,Demo, G.,Dutcher, R.C.,Tanaka Hall, T.M.,Zamore, P.D.,Korostelev, A.A. (deposition date: 2022-06-23, release date: 2022-11-16, Last modification date: 2024-06-12)
Primary citationJouravleva, K.,Golovenko, D.,Demo, G.,Dutcher, R.C.,Hall, T.M.T.,Zamore, P.D.,Korostelev, A.A.
Structural basis of microRNA biogenesis by Dicer-1 and its partner protein Loqs-PB.
Mol.Cell, 82:4049-4063.e6, 2022
Cited by
PubMed Abstract: In animals and plants, Dicer enzymes collaborate with double-stranded RNA-binding domain (dsRBD) proteins to convert precursor-microRNAs (pre-miRNAs) into miRNA duplexes. We report six cryo-EM structures of Drosophila Dicer-1 that show how Dicer-1 and its partner Loqs‑PB cooperate (1) before binding pre-miRNA, (2) after binding and in a catalytically competent state, (3) after nicking one arm of the pre-miRNA, and (4) following complete dicing and initial product release. Our reconstructions suggest that pre-miRNA binds a rare, open conformation of the Dicer‑1⋅Loqs‑PB heterodimer. The Dicer-1 dsRBD and three Loqs‑PB dsRBDs form a tight belt around the pre-miRNA, distorting the RNA helix to place the scissile phosphodiester bonds in the RNase III active sites. Pre-miRNA cleavage shifts the dsRBDs and partially closes Dicer-1, which may promote product release. Our data suggest a model for how the Dicer‑1⋅Loqs‑PB complex affects a complete cycle of pre-miRNA recognition, stepwise endonuclease cleavage, and product release.
PubMed: 36182693
DOI: 10.1016/j.molcel.2022.09.002
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (4.02 Å)
Structure validation

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