ZAR1 pathogenic variants disrupt maternal mRNA storage and cause oocyte maturation defects in humans

Zygote arrest 1 (Zar1) was one of the earliest identified maternal-effect genes that function during the maternal-to-zygotic transition (MZT) in mice. However, the role of human ZAR1 remains unclear. In this study, we investigated the association of ZAR1 gene variants with infertility in women, focusing on their impact on oocyte maturation and early embryonic development. Using whole-exome sequencing, we identified homozygous and compound heterozygous ZAR1 variants in two independent families with female patients diagnosed with primary infertility owing to oocyte maturation and early embryonic arrest. Functional analysis revealed that the V118A variant disrupted the localization of ZAR1 to the mitochondria-associated ribonucleoprotein domain (MARDO) structure, which is a key mRNA storage site in oocytes. The R397Q and S121* mutations impaired ZAR1’s RNA-binding capability, indirectly affecting its subcellular localization and the integrity of MARDO. These variants disrupted MARDO formation and function, leading to defective oocyte maturation and early embryonic development. This study highlights the critical roles of ZAR1 and MARDO in human reproduction and provides insights into the molecular mechanisms underlying some forms of female infertility.

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Publication Details

Journal
Cellular and Molecular Life Sciences
Published
2025-12-20
DOI
https://doi.org/10.1007/s00018-025-06000-4
Citations
2
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
1.61

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article

ZAR1 pathogenic variants disrupt maternal mRNA storage and cause oocyte maturation defects in humans

Quanlong Lü, Heng‐Yu Fan, Xiu-Quan Liao, Shaoyuan Liu et al.
2 citations
Cellular and Molecular Life Sciences
RNA regulation and disease
1.61
article

ZAR1 pathogenic variants disrupt maternal mRNA storage and cause oocyte maturation defects in humans

Quanlong Lü, Heng‐Yu Fan, Xiu-Quan Liao, Shaoyuan Liu, Changlong Zhang, Qian‐Qian Sha, Shuai Zhao, Jiangtao Zhang, Jun Wen, Han Zhao, Wei Zheng, Wei Su, Yan Zhu, Fei Gong, Ge Lin, Yang Wang
article en
2 citations

Abstract

Zygote arrest 1 (Zar1) was one of the earliest identified maternal-effect genes that function during the maternal-to-zygotic transition (MZT) in mice. However, the role of human ZAR1 remains unclear. In this study, we investigated the association of ZAR1 gene variants with infertility in women, focusing on their impact on oocyte maturation and early embryonic development. Using whole-exome sequencing, we identified homozygous and compound heterozygous ZAR1 variants in two independent families with female patients diagnosed with primary infertility owing to oocyte maturation and early embryonic arrest. Functional analysis revealed that the V118A variant disrupted the localization of ZAR1 to the mitochondria-associated ribonucleoprotein domain (MARDO) structure, which is a key mRNA storage site in oocytes. The R397Q and S121* mutations impaired ZAR1’s RNA-binding capability, indirectly affecting its subcellular localization and the integrity of MARDO. These variants disrupted MARDO formation and function, leading to defective oocyte maturation and early embryonic development. This study highlights the critical roles of ZAR1 and MARDO in human reproduction and provides insights into the molecular mechanisms underlying some forms of female infertility.

Cellular and Molecular Life SciencesVol. 83(1)
Guangdong University of Technology (CN), Central South University (CN), Shandong University (CN), Second Affiliated Hospital of Guangzhou Medical University (CN), Reproductive & Genetic Hospital CITIC-Xiangya (CN), Guangdong Provincial Hospital of Traditional Chinese Medicine (CN), Guangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality (CN), Shandong Provincial Hospital (CN), Institut de Médecine de la Reproduction (FR), Guangdong Provincial People's Hospital (CN), Shandong First Medical University (CN), Southern Medical University (CN), Zhejiang University (CN), Guangzhou Medical University (CN)
National Natural Science Foundation of China, Nanjing Medical University
Openalex Percentile: Top 14%
RNA regulation and disease
1.61
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