GALNTL5 binds GalNAc and is required for migration through the uterotubal junction and sperm-zona pellucida binding

T Taichi Noda (Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University) R Reika Uriu D Daisuke Mashiko (Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka) H Hina Shinohara Y Yongcun Qu A Ayumu Taira R Ryan M. Matzuk D Duri Tahala M Motochika Nakano K Kimi Araki (Division of Developmental Genetics, Institute of Resource Development and Analysis, Kumamoto University) Z Zhifeng Yu Y Ying Zhang M Martin M. Matzuk (Center for Drug Discovery, Department of Pathology & Immunology, Baylor College of Medicine) M Masahito Ikawa (Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka)

Abstract

Abstract More than 20 genes expressed in the male reproductive tract have been identified as essential factors for sperm migration to and through the utero-tubal junction (UTJ), and they are divided into ADAM3-dependent and ADAM3-independent pathways. In parallel, sperm having UTJ migration defects also show impaired binding to the zona pellucida (ZP). Herein, we demonstrate that knockout of Galntl5, encoding a sperm surface protein, causes impaired sperm binding with the UTJ and ZP, and null males have severe infertility. GALNTL5 appreciably disappears in sperm lacking Adam3 or Lypd4, required for ADAM3-dependent and ADAM3-independent pathways, and GALNTL5 binds to N-acetylgalactosamine (GalNAc) distributed on the UTJ and ZP. Blockage of GalNAc decreases the number of sperm binding to the UTJ and ZP. Thus, we unveil that GALNTL5 is a responsible factor for UTJ migration and sperm-ZP binding, and that sperm bind to the UTJ and ZP through interaction of GALNTL5 and GalNAc.

Article Details

Volume / Issue Vol. 16, Issue 1
Published September 17, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (14)

T

Taichi Noda

Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University

R

Reika Uriu

D

Daisuke Mashiko

Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka

H

Hina Shinohara

Y

Yongcun Qu

A

Ayumu Taira

R

Ryan M. Matzuk

D

Duri Tahala

M

Motochika Nakano

K

Kimi Araki

Division of Developmental Genetics, Institute of Resource Development and Analysis, Kumamoto University

Z

Zhifeng Yu

Y

Ying Zhang

M

Martin M. Matzuk

Center for Drug Discovery, Department of Pathology & Immunology, Baylor College of Medicine

M

Masahito Ikawa

Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka