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9KBZ

Cryo-EM structure of DCL4-DRB4CTD-dsRNA complex

Summary for 9KBZ
Entry DOI10.2210/pdb9kbz/pdb
EMDB information62235
DescriptorDicer-like protein 4, Double-stranded RNA-binding protein 4, RNA (57-MER), ... (5 entities in total)
Functional Keywordsdcl4, drb4, sirna, dicer, rna binding protein/rna, rna binding protein-rna complex
Biological sourceArabidopsis thaliana (thale cress)
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Total number of polymer chains4
Total formula weight243426.64
Authors
Wang, C.,Du, J. (deposition date: 2024-10-31, release date: 2026-02-18, Last modification date: 2026-04-15)
Primary citationWang, C.,Chi, C.,Liu, Y.,Zhao, J.,Wang, Q.,Wang, N.,Zhang, Z.,Jiang, K.,Xue, Y.,Li, Y.,Wang, P.,Zhai, J.,Guo, H.,Du, J.
Molecular basis of DRB4-assisted long RNA processing and 21-nucleotide siRNA biogenesis by DCL4 in plants.
Nat.Plants, 12:512-519, 2026
Cited by
PubMed Abstract: Small RNAs, including microRNA, small interfering RNA (siRNA) and PIWI-interacting RNA, are regulatory RNAs that play critical roles in gene regulation, development, viral defence and environmental response. The biogenesis of microRNA and siRNA relies on the Dicer family ribonucleases to capture, measure and cleave their double-stranded RNA substrates. In Arabidopsis, DICER-LIKE 4 (DCL4) produces 21-nucleotide siRNA in association with Double-Stranded RNA-Binding Protein 4 (DRB4) for post-transcriptional gene silencing. Here we determined the structures of the DCL4-RNA complex in a dicing-competent conformation and the DCL4-DRB4-RNA complex in a pre-dicing conformation. DCL4 measures 21 nucleotides along RNA between its PAZ and RNase III domains to determine the product siRNA length. A DCL4-specific loop locates the second double-stranded RNA binding domain of DCL4 and DRB4 to a distal position of the substrate RNA, yielding a preference for long RNA substrates. Our studies demonstrate the molecular basis of substrate recognition, length measurement and long RNA preference by the DCL4-DRB4 complex for 21-nucleotide siRNA biogenesis in plants.
PubMed: 41781744
DOI: 10.1038/s41477-026-02236-5
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.18 Å)
Structure validation

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