Gatm ablation disrupts spermatogenesis by impairing ribosome biogenesis and coupling defective steroid biosynthesis to immunoglobulin silencing

Background Glycine amidinotransferase (GATM) catalyzes the rate-limiting step in creatine biosynthesis, a pathway essential for cellular energy buffering in tissues with high metabolic demands. While its roles in muscle and brain are well established, the function of GATM in testicular development and spermatogenesis remains largely unexplored. Methods We generated a constitutive Gatm knockout mouse model using CRISPR/Cas9 technology. Comprehensive phenotypic characterization was performed through histological analysis, transmission electron microscopy (TEM), and transcriptomic profiling of whole testes and purified spermatozoa from Gatm , heterozygous ( Gatm ), and wild-type (WT) mice. Results Gatm deficiency resulted in severe testicular atrophy, disorganized seminiferous tubules with epithelial thinning (reduced to 2–3 layers), and interstitial edema. Spermatogenesis was arrested, leading to dramatically reduced sperm density. Ultrastructural analysis revealed hallmark features of cacospermia, including mitochondrial depletion in the midpiece and nuclear vacuolization. Transcriptomic profiling demonstrated widespread dysregulation: testicular tissues showed downregulation of ribosome biogenesis and mitochondrial complex assembly pathways, whereas mature spermatozoa exhibited impaired steroid biosynthesis and ion transport. Notably, multiple immunoglobulin variable region genes (e.g., Ighv14-1 , Igkv19-93 ) were completely transcriptionally silenced specifically in Gatm -deficient testes. Conclusion Our findings establish GATM as a multifunctional regulator of spermatogenesis, integrating creatine-dependent energy metabolism with translational capacity, organelle architecture, and immune-related gene regulation. The coordinated disruption of mitochondrial and ribosomal pathways provides a novel mechanistic framework for understanding the metabolic origins of male infertility.

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Publication Details

Journal
Frontiers in Cell and Developmental Biology
Published
2026-03-12
DOI
https://doi.org/10.3389/fcell.2026.1786659
Primary Topic
Muscle metabolism and nutrition
Type
article
Field-Weighted Citation Impact
0.00

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article

Gatm ablation disrupts spermatogenesis by impairing ribosome biogenesis and coupling defective steroid biosynthesis to immunoglobulin silencing

Lin Yang, Lixiang Chen, Mengmin Zhu, Xiaohui Zhou et al.
Frontiers in Cell and Developmental Biology
Muscle metabolism and nutrition
article

Gatm ablation disrupts spermatogenesis by impairing ribosome biogenesis and coupling defective steroid biosynthesis to immunoglobulin silencing

Lin Yang, Lixiang Chen, Mengmin Zhu, Xiaohui Zhou, Shun Li, Hanqing Wu
article en

Abstract

Background Glycine amidinotransferase (GATM) catalyzes the rate-limiting step in creatine biosynthesis, a pathway essential for cellular energy buffering in tissues with high metabolic demands. While its roles in muscle and brain are well established, the function of GATM in testicular development and spermatogenesis remains largely unexplored. Methods We generated a constitutive Gatm knockout mouse model using CRISPR/Cas9 technology. Comprehensive phenotypic characterization was performed through histological analysis, transmission electron microscopy (TEM), and transcriptomic profiling of whole testes and purified spermatozoa from Gatm , heterozygous ( Gatm ), and wild-type (WT) mice. Results Gatm deficiency resulted in severe testicular atrophy, disorganized seminiferous tubules with epithelial thinning (reduced to 2–3 layers), and interstitial edema. Spermatogenesis was arrested, leading to dramatically reduced sperm density. Ultrastructural analysis revealed hallmark features of cacospermia, including mitochondrial depletion in the midpiece and nuclear vacuolization. Transcriptomic profiling demonstrated widespread dysregulation: testicular tissues showed downregulation of ribosome biogenesis and mitochondrial complex assembly pathways, whereas mature spermatozoa exhibited impaired steroid biosynthesis and ion transport. Notably, multiple immunoglobulin variable region genes (e.g., Ighv14-1 , Igkv19-93 ) were completely transcriptionally silenced specifically in Gatm -deficient testes. Conclusion Our findings establish GATM as a multifunctional regulator of spermatogenesis, integrating creatine-dependent energy metabolism with translational capacity, organelle architecture, and immune-related gene regulation. The coordinated disruption of mitochondrial and ribosomal pathways provides a novel mechanistic framework for understanding the metabolic origins of male infertility.

Frontiers in Cell and Developmental BiologyVol. 14
Shanghai Normal University (CN), Shanghai Public Health Clinical Center (CN)
Shanghai Municipal Health Commission
Affordable and clean energy
Openalex Percentile: Top 25%
Muscle metabolism and nutrition
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