TEX38 localizes ZDHHC19 to the plasma membrane and regulates sperm head morphogenesis in mice

Y Yuki Kaneda (Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka) Y Yonggang Lu (Premium Research Institute for Human Metaverse Medicine, Osaka University) J Jiang Sun (Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University) K Keisuke Shimada (Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University) C Chihiro Emori (Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka) T Taichi Noda (Department of Experimental Genome Research, Research Institute for Microbial Diseases, Osaka University) T Takayuki Koyano (Division of Molecular Genetics, Shigei Medical Research Institute) M Makoto Matsuyama (Division of Molecular Genetics, Shigei Medical Research Institute) H Haruhiko Miyata (Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka) M Masahito Ikawa (Department of Experimental Genome Research, Research Institute for Microbial Diseases, The University of Osaka)

Abstract

Sperm morphogenesis is a tightly regulated differentiation process, disruption of which leads to sperm malfunction and male infertility. Here, we show that Tex38 knockout (KO) male mice are infertile. Tex38 KO spermatids exhibit excess retention of residual cytoplasm around the head, resulting in abnormal sperm morphology with backward head bending. TEX38 interacts and colocalizes with ZDHHC19, a testis-enriched acyltransferase catalyzing protein S-palmitoylation, at the plasma membrane of spermatids. ZDHHC19 and TEX38 are each downregulated in mouse testes lacking the other protein. TEX38 stabilizes and localizes ZDHHC19 to the plasma membrane of cultured cells and vice versa, consolidating their interdependence. Mice deficient in ZDHHC19 or harboring a C142S mutation that disables the palmitoyltransferase activity of ZDHHC19 display phenotypes resembling those of Tex38 KO mice. Strikingly, ZDHHC19 palmitoylates ARRDC5, an arrestin family protein regulating sperm differentiation. Overall, our findings indicate that TEX38 forms a stable complex with ZDHHC19 at the plasma membrane of spermatids, which governs downstream S-palmitoylation of proteins essential for morphological transformation of spermatids.

Article Details

Volume / Issue Vol. 122, Issue 10
Published March 11, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (10)

Y

Yuki Kaneda

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

Y

Yonggang Lu

Premium Research Institute for Human Metaverse Medicine, Osaka University

J

Jiang Sun

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

K

Keisuke Shimada

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

C

Chihiro Emori

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

T

Taichi Noda

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

T

Takayuki Koyano

Division of Molecular Genetics, Shigei Medical Research Institute

M

Makoto Matsuyama

Division of Molecular Genetics, Shigei Medical Research Institute

H

Haruhiko Miyata

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

M

Masahito Ikawa

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