ARMH2 is a cytosolic component of CatSper crucial for sperm function

Sperm capacitation and fertilization are highly regulated by Ca<sup>2+</sup> signaling. CatSper, a sperm-specific calcium channel, plays a crucial role in sperm hyperactivated motility and fertility by mediating Ca<sup>2+</sup> influx into sperm. CatSper is the most complicated ion channel known, comprising the pore-forming CATSPER1-4 and multiple auxiliary subunits. However, our previous structural study of mouse CatSper suggests the presence of potential component(s) that remain to be identified. The identity and functional significance of the missing piece(s) of CatSper remain elusive. Here, by combining cryo-EM, mass spectrometry, AlphaFold structure prediction, and coevolutionary analysis, we identify armadillo-like helical domain containing 2 (ARMH2) as a cytosolic component of CatSper. ARMH2 forms a cytosolic ternary subcomplex with EFCAB9 and CATSPERζ, which contributes to the stable assembly of the linear arrangement of CatSper nanodomains along the sperm tail and regulates the pH and Ca<sup>2+</sup> sensitivity of the channel. Loss of ARMH2 leads to compromised physiological activation of CatSper, thereby resulting in asthenozoospermia and severe subfertility. These findings show that ARMH2 is crucial for sperm function and provide fresh insights into the composition and functional regulation of CatSper. The integrated methodology employed in identifying ARMH2 also provides valuable approaches for discovering uncharacterized components in other protein complexes.

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Publication Details

Journal
Nature Communications
Published
2025-11-21
DOI
https://doi.org/10.1038/s41467-025-65952-0
Citations
1
Primary Topic
Sperm and Testicular Function
Type
article
Field-Weighted Citation Impact
1.70

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article

ARMH2 is a cytosolic component of CatSper crucial for sperm function

Yongdeng Zhang, Yanfei Ru, Yi Zhu, Mingxi Liu et al.
1 citations
Nature Communications
Sperm and Testicular Function
1.70
article

ARMH2 is a cytosolic component of CatSper crucial for sperm function

Yongdeng Zhang, Yanfei Ru, Yi Zhu, Mingxi Liu, Xuhui Zeng, Carlo De Rito, Qingqing Zhao, Honghan Cheng, Zijing Yu, Yan Zhen, Shiyi Lin, Jean‐Ju Chung, Jianping Wu, Qikui Xu, Riccardo Percudani, Min Jiang, Shaojie Wang, Hang Won Kang, Shuya Sun, Rui Sun, Xiaofang Huang, Giulia Sassi
article en
1 citations

Abstract

Sperm capacitation and fertilization are highly regulated by Ca<sup>2+</sup> signaling. CatSper, a sperm-specific calcium channel, plays a crucial role in sperm hyperactivated motility and fertility by mediating Ca<sup>2+</sup> influx into sperm. CatSper is the most complicated ion channel known, comprising the pore-forming CATSPER1-4 and multiple auxiliary subunits. However, our previous structural study of mouse CatSper suggests the presence of potential component(s) that remain to be identified. The identity and functional significance of the missing piece(s) of CatSper remain elusive. Here, by combining cryo-EM, mass spectrometry, AlphaFold structure prediction, and coevolutionary analysis, we identify armadillo-like helical domain containing 2 (ARMH2) as a cytosolic component of CatSper. ARMH2 forms a cytosolic ternary subcomplex with EFCAB9 and CATSPERζ, which contributes to the stable assembly of the linear arrangement of CatSper nanodomains along the sperm tail and regulates the pH and Ca<sup>2+</sup> sensitivity of the channel. Loss of ARMH2 leads to compromised physiological activation of CatSper, thereby resulting in asthenozoospermia and severe subfertility. These findings show that ARMH2 is crucial for sperm function and provide fresh insights into the composition and functional regulation of CatSper. The integrated methodology employed in identifying ARMH2 also provides valuable approaches for discovering uncharacterized components in other protein complexes.

Nature CommunicationsVol. 16(1)
University of Parma (IT), Nantong University (CN), Fudan University (CN), Westlake University (CN), Yale University (US), Nanjing Medical University (CN)
Westlake University, National Natural Science Foundation of China, Natural Science Foundation of Zhejiang Province
Openalex Percentile: Top 11%
Sperm and Testicular Function
1.70
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