Abstract
SummaryMammalian sperm-egg adhesion depends on the trans-interaction between the sperm-specific type I glycoprotein IZUMO1 and its oocyte-specific GPI-anchored receptor JUNO. However, the mechanisms and proteins (fusogens) which mediate the following step of gamete fusion remain unknown. Using live imaging and content mixing assays in a heterologous system and structure-guided mutagenesis, we unveil an unexpected function for IZUMO1 in cell-to-cell fusion. We show that IZUMO1 alone is sufficient to induce fusion, and that this ability is retained in a mutant unable to bind JUNO. On the other hand, a triple mutation in exposed aromatic residues prevents this fusogenic activity without impairing JUNO interaction. Our findings suggest a second, crucial function for IZUMO1 as a unilateral mouse gamete fusogen.HighlightsIZUMO1 expression in somatic cells in culture induces cell-to-cell fusionThe fusogenic activity of IZUMO1 is unilateralCell fusion is independent of the binding of IZUMO1 to JUNOIZUMO1-mediated cell merger depends on its transmembrane domain, and three solvent-exposed aromatic residuesGraphical abstract
Publisher
Cold Spring Harbor Laboratory
Cited by
3 articles.
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