Summary information and primary citation
- PDB-id
-
8d6j;
DSSR-derived features in text and
JSON formats; DNAproDB
- Class
- RNA binding protein-RNA
- Method
- X-ray (2.5 Å)
- Summary
- Human ago2 bound to mir122(21nt) with piwi loop swapped
to atago10 sequence
- Reference
-
Xiao Y, Liu TM, MacRae IJ (2023): "A tiny
loop in the Argonaute PIWI domain tunes small RNA seed
strength." Embo Rep., 24,
e55806. doi: 10.15252/embr.202255806.
- Abstract
- Argonaute (AGO) proteins use microRNAs (miRNAs) and
small interfering RNAs (siRNAs) as guides to regulate gene
expression in plants and animals. AGOs that use miRNAs in
bilaterian animals recognize short (6-8 nt.) elements
complementary to the miRNA seed region, enabling each miRNA
to interact with hundreds of otherwise unrelated targets.
By contrast, AGOs that use miRNAs in plants employ longer
(> 13 nt.) recognition elements such that each miRNA
silences a small number of physiologically related targets.
Here, we show that this major functional distinction
depends on a minor structural difference between plant and
animal AGO proteins: a 9-amino acid loop in the PIWI
domain. Swapping the PIWI loop from human Argonaute2
(HsAGO2) into Arabidopsis Argonaute10 (AtAGO10) increases
seed strength, resulting in animal-like miRNA targeting.
Conversely, swapping the plant PIWI loop into HsAGO2
reduces seed strength and accelerates the turnover of
cleaved targets. The loop-swapped HsAGO2 silences targets
more potently, with reduced miRNA-like targeting, than
wild-type HsAGO2 in mammalian cells. Thus, tiny structural
differences can tune the targeting properties of AGO
proteins for distinct biological roles.