Structural and functional insights into IZUMO1 recognition by JUNO in mammalian fertilization

Kazuki Kato(The University of Tokyo), Yuhkoh Satouh(The University of Osaka), Hiroshi Nishimasu(The University of Tokyo), Arisa Kurabayashi(The University of Tokyo), Junko Morita(The University of Tokyo), Yoshitaka Fujihara(The University of Osaka), Asami Oji(The University of Osaka), Ryuichiro Ishitani(The University of Tokyo), Masahito Ikawa(The University of Osaka), Osamu Nureki(The University of Tokyo)
Nature Communications
July 15, 2016
Cited by 94Open Access
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Abstract

Sperm-egg fusion is the critical step in mammalian fertilization, and requires the interaction between IZUMO1 on the sperm surface and JUNO (also known as folate receptor (FR) 4 or IZUMO1R) on the egg surface. Whereas other FRs bind and uptake folates, JUNO binds IZUMO1 and establishes the cell-cell adhesion. However, the mechanism of IZUMO1 recognition by JUNO has remained elusive. Here we report the crystal structure of mouse JUNO, at 2.3 Å resolution. A structural comparison of JUNO with the FRs revealed that JUNO and the FRs have similar overall structures, but JUNO lacks the folate-binding pocket, thereby explaining the inability of JUNO to bind folate. Further complementation of Juno knockout eggs with mutant Juno messenger RNAs revealed that the conserved, surface-exposed tryptophan residue of JUNO is required for sperm binding and fertilization. Our structure-based in vivo functional analyses provide a framework towards a mechanistic understanding of mammalian gamete recognition.


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