C11orf94/Frey is a key regulator for male fertility by controlling Izumo1 complex assembly

Author:

Contreras Whendy1ORCID,Wiesehöfer Caroline2ORCID,Schreier Dora3,Leinung Nadja1,Peche Petra1ORCID,Wennemuth Gunther2ORCID,Gentzel Marc4ORCID,Schröder Bernd1ORCID,Mentrup Torben1ORCID

Affiliation:

1. Institute of Physiological Chemistry, Technische Universität Dresden, Dresden, Germany.

2. Department of Anatomy, University Hospital, University of Duisburg-Essen, Essen, Germany.

3. CRISPR-Cas9 Facility, Experimental Center of the Medical Faculty Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

4. Core Facility Molecular Analysis–Mass Spectrometry, Center for Molecular and Cellular Bioengineering (CMCB), Technische Universität Dresden, Dresden, Germany.

Abstract

Although gamete fusion represents the central event in sexual reproduction, the required protein machinery is poorly defined. In sperm cells, Izumo1 and several Izumo1-associated proteins play an essential role for this process. However, so far, the mechanisms underlying transport and maturation of Izumo1 and its incorporation into high molecular weight complexes are incompletely defined. Here, we provide a detailed characterization of the C11orf94 protein, which we rename Frey, which provides a platform for the assembly of Izumo1 complexes. By retaining Izumo1 in the endoplasmic reticulum, Frey facilitates its incorporation into high molecular weight complexes. To fulfill its function, the unstable Frey protein is stabilized within the catalytic center of an intramembrane protease. Loss of Frey results in reduced assembly of Izumo1 complexes and male infertility due to impaired gamete fusion. Collectively, these findings provide mechanistic insights into the early biogenesis and functional relevance of Izumo1 complexes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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