9SHP

Cryo-EM structure of the endogeneous MIWI in complex with pachytene piRNA at 3.3A

Summary for 9SHP

• Entry DOI: 10.2210/pdb9shp/pdb
• EMDB information: 54907
• Descriptor: Piwi-like protein 1, RNA (5'-R(P*UP*UP*AP*CP*CP*A)-3'), MAGNESIUM ION (3 entities in total)
• Functional Keywords: miwi, piwil1, pirna, slicer, pachytene pirna, rna binding protein
• Biological source: Mus musculus (house mouse); More
• Total number of polymer chains: 2
• Total formula weight: 101611.64

Authors

Raad, N.G.,Fernandez-Rodriguez, C.,Pandey, R.R.,Mohammed, I.,Uchikawa, E.,Burger, F.,Homolka, D.,Pillai, R.S. (deposition date: 2025-08-27, release date: 2026-01-21)

Primary citation

Raad, N.,Fernandez-Rodriguez, C.,Pandey, R.R.,Mohammed, I.,Uchikawa, E.,Burger, F.,Homolka, D.,Pillai, R.S.
Structure of the MIWI endoribonuclease bound to pachytene piRNAs from mouse testes.
Cell Rep, 45:116804-116804, 2026

PubMed Abstract: PIWI-interacting RNAs (piRNAs) guide PIWI endoribonucleases to destroy transposon transcripts, ensuring animal fertility. Here, we report the cryo-electron microscopy structure of the MIWI-pachytene piRNA complex isolated from mouse testes. The piRNA is held via non-specific charge-based interactions with the RNA backbone and by specific recognition of the first nucleotide uridine by residues within the MID and PIWI domains. The first six nucleotides of the guide RNA take up the A-form conformation to facilitate pairing with the target. The RNA channel is wider than that observed in insect PIWI proteins, explaining the tolerance for piRNA seed:target mismatches. The PIWI endonuclease domain is in an inactive "un-plugged" state, with the loop containing a catalytic residue (E671) requiring structural re-orientation for activity. Furthermore, the PIWI domain reveals a conserved pre-formed pocket that may serve to accommodate a conserved tryptophan from the interacting factor GTSF1 to promote small RNA-guided endoribonuclease activity.

PubMed: 41528842
DOI: 10.1016/j.celrep.2025.116804

Experimental method

ELECTRON MICROSCOPY (3.7 Å)