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Composite SMG5-1 SMG6 PIN domain formation is essential for NMD

ABSTRACT: Nonsense-mediated mRNA decay (NMD) relies on the coordinated assembly and action of multiple protein factors. Degradation of target mRNAs begins with endonucleolytic cleavage near premature stop codons, but the mechanisms of endonuclease activation and regulation remain unclear. Using structural predictions, biochemical in vitro assays, and cell-based NMD analysis, we show that SMG5 and SMG6 interact via their PIN domains to form a composite interface (cPIN) with full endonuclease activity. In vitro reconstituted SMG5-SMG6 cPIN heterodimers show high activity, as SMG5 completes the SMG6 active site and substrate binding site. Mutations in residues at their predicted interaction surfaces, RNA-binding sites, or active-site attenuate or abolish cPIN activity in vitro and impair cellular NMD. Our findings demonstrate how paralogous PIN domains complement each other to assemble a highly active endonuclease in NMD, providing a structural and mechanistic explanation for efficient NMD substrate degradation.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

SUBMITTER: Barbara Steigenberger

LAB HEAD: Elena Conti

PROVIDER: PXD072588 | Pride | 2026-01-30

REPOSITORIES: Pride

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			Action	DRS
	20251201_ECL1_ENO9_68min_BaSt_SA_F-50-60_Orbi5988_Sample01.raw	Raw
	20251201_ECL1_ENO9_68min_BaSt_SA_F-50-60_Orbi5988_Sample01_Crosslinks.txt	Txt
	20251202_ECL1_ENO9_68min_BaSt_SA_F-45-55_Orbi5988_SDC_Sample01.raw	Raw
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