9K9P image
Deposition Date 2024-10-27
Release Date 2026-02-18
Last Version Date 2026-04-15
Entry Detail
PDB ID:
9K9P
Title:
crystal structure of Arabidopsis DCL4 dsRBD2 in complex with DRB4 CTD
Biological Source:
Source Organism(s):
Expression System(s):
Method Details:
Experimental Method:
Resolution:
1.42 Å
R-Value Free:
0.19
R-Value Work:
0.17
R-Value Observed:
0.17
Space Group:
P 21 21 21
Macromolecular Entities
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Dicer-like protein 4
Gene (Uniprot):DCL4
Chain IDs:A
Chain Length:89
Number of Molecules:1
Biological Source:Arabidopsis thaliana
Structures with similar UniProt ID
Protein Blast
Polymer Type:polypeptide(L)
Molecule:Double-stranded RNA-binding p
Gene (Uniprot):DBR4
Chain IDs:B
Chain Length:54
Number of Molecules:1
Biological Source:Arabidopsis thaliana
Primary Citation
Molecular basis of plant DCL4 action that outcompetes DCL2.
Nat.Plants 12 556 570 (2026)
PMID: 41781745 DOI: 10.1038/s41477-026-02243-6

Abstact

Small RNAs regulate eukaryotic development and immunity. In plants, multiple DICER-LIKE (DCL) proteins produce distinct small RNAs that play diverse functions. These DCL proteins act in a hierarchical manner, with DCL4 outcompeting DCL2 being particularly important for optimal gene expression and plant growth. However, the mechanism of this hierarchical action remains unclear. Here we reveal that the second double-stranded-RNA-binding domain (dsRBD2) of DCL4 interacts with DSRNA BINDING PROTEIN 4 (DRB4), a cofactor essential for DCL4's function. DRB4 dictates the relative biogenesis of 21- and 22-nucleotide small interfering RNAs derived from TAS loci and coding transcripts. All DCL2 proteins in seed plants lack dsRBD2; however, fusing dsRBD2 to DCL2 enhances its activity, leading to massive production of coding-transcript-derived small interfering RNAs, as well as growth defects and activated stress responses. These findings demonstrate the central role of the dsRBD2-DRB4 module, which enables DCL4 to outcompete DCL2, thereby preventing detrimental gene silencing.

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Primary Citation of related structures
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