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7YZ4

Mouse endoribonuclease Dicer (composite structure)

Summary for 7YZ4
Entry DOI10.2210/pdb7yz4/pdb
Related7YYM 7YYN
EMDB information14383 14384 14387 15297 15298 15299
DescriptorEndoribonuclease Dicer (1 entity in total)
Functional Keywordsendoribonuclease, gene silencing, post-transcriptional, catalytic enzyme, cytoplasm, rna binding protein
Biological sourceMus musculus (house mouse)
Total number of polymer chains1
Total formula weight226809.59
Authors
Zanova, M.,Zapletal, D.,Kubicek, K.,Stefl, R.,Pinkas, M.,Novacek, J. (deposition date: 2022-02-18, release date: 2022-11-16, Last modification date: 2024-07-17)
Primary citationZapletal, D.,Taborska, E.,Pasulka, J.,Malik, R.,Kubicek, K.,Zanova, M.,Much, C.,Sebesta, M.,Buccheri, V.,Horvat, F.,Jenickova, I.,Prochazkova, M.,Prochazka, J.,Pinkas, M.,Novacek, J.,Joseph, D.F.,Sedlacek, R.,Bernecky, C.,O'Carroll, D.,Stefl, R.,Svoboda, P.
Structural and functional basis of mammalian microRNA biogenesis by Dicer.
Mol.Cell, 82:4064-4079.e13, 2022
Cited by
PubMed Abstract: MicroRNA (miRNA) and RNA interference (RNAi) pathways rely on small RNAs produced by Dicer endonucleases. Mammalian Dicer primarily supports the essential gene-regulating miRNA pathway, but how it is specifically adapted to miRNA biogenesis is unknown. We show that the adaptation entails a unique structural role of Dicer's DExD/H helicase domain. Although mice tolerate loss of its putative ATPase function, the complete absence of the domain is lethal because it assures high-fidelity miRNA biogenesis. Structures of murine Dicer•-miRNA precursor complexes revealed that the DExD/H domain has a helicase-unrelated structural function. It locks Dicer in a closed state, which facilitates miRNA precursor selection. Transition to a cleavage-competent open state is stimulated by Dicer-binding protein TARBP2. Absence of the DExD/H domain or its mutations unlocks the closed state, reduces substrate selectivity, and activates RNAi. Thus, the DExD/H domain structurally contributes to mammalian miRNA biogenesis and underlies mechanistical partitioning of miRNA and RNAi pathways.
PubMed: 36332606
DOI: 10.1016/j.molcel.2022.10.010
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.84 Å)
Structure validation

226707

數據於2024-10-30公開中

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