
Mutations that disrupt cotranslational membrane integration (V276T) or tertiary structure (W107A) of the gonadotropin-releasing hormone receptor (GnRHR) form distinct epistatic interactions that depend on the mechanism and severity of destabilization.


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Many membrane proteins are prone to misfolding, which compromises their functional expression at the plasma membrane. This is particularly true for the mammalian gonadotropin-releasing hormone receptor GPCRs (GnRHR). We recently demonstrated that evolutionary GnRHR modifications appear to have coincided with adaptive changes in cotranslational folding efficiency. Though protein stability is known to shape evolution, it is unclear how cotranslational folding constraints modulate the synergistic, epistatic interactions between mutations. We therefore compared the pairwise interactions formed by mutations that disrupt the membrane topology (V276T) or tertiary structure (W107A) of GnRHR. Using deep mutational scanning, we evaluated how the plasma membrane expression of these variants is modified by hundreds of secondary mutations. An analysis of 251 mutants in three genetic backgrounds reveals that V276T and W107A form distinct epistatic interactions that depend on both the severity and the mechanism of destabilization. V276T forms predominantly negative epistatic interactions with destabilizing mutations in soluble loops. In contrast, W107A forms positive interactions with mutations in both loops and transmembrane domains that reflect the diminishing impacts of the destabilizing mutations in variants that are already unstable. These findings reveal how epistasis is remodeled by conformational defects in membrane proteins and in unstable proteins more generally.

Impact Statement Many of the synergistic interactions between mutations within a gene are modified in the context of unstable proteins in a manner that depends on how the variants promote misfolding in the cell.

### Competing Interest Statement

The authors have declared no competing interest.

Divergent Folding-Mediated Epistasis Among Unstable Membrane Protein Variants

divergent-epistatic-interactions-arise-from-distinct-folding-defects-in-an-unstable-membrane-protein


Divergent Epistatic Interactions Arise from Distinct Folding Defects in an Unstable Membrane Protein
