The New Nexin‐Dynein Regulatory Complex Component <scp>CCDC153</scp> Is Dispensable for Ciliary Motility and Fertility in Mice

The nexin-dynein regulatory complex (N-DRC) is an essential axonemal structure for ciliary and flagellar motility. Coiled-coil domain containing 153 (CCDC153) has recently been identified as a new N-DRC component in Tetrahymena thermophila. However, the physiological function of its mammalian homolog remains unknown. Here, we generated a Ccdc153 knockout mouse model and explored its functional association with motile cilia. We found that CCDC153 was highly expressed in the motile cilia-abundant tissues and localized to the axonemal lumen in motile cilia. However, Ccdc153 knockout mice were viable and exhibited normal brain ventricles and fertility. Overall, our results suggest that CCDC153 is dispensable for ciliary motility in brain ventricles and sperm movement, indicating that CCDC153 is not a potential causative gene in human ciliopathies.

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Journal
Cytoskeleton
Published
2025-10-08
DOI
https://doi.org/10.1002/cm.70053
Primary Topic
Genetic and Kidney Cyst Diseases
Type
article
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article

The New Nexin‐Dynein Regulatory Complex Component CCDC153 Is Dispensable for Ciliary Motility and Fertility in Mice

Huijie Zhao, Xunshuo Liu, Shanshan Nai, Yanjie Zheng
Cytoskeleton
Genetic and Kidney Cyst Diseases
article

The New Nexin‐Dynein Regulatory Complex Component CCDC153 Is Dispensable for Ciliary Motility and Fertility in Mice

Huijie Zhao, Xunshuo Liu, Shanshan Nai, Yanjie Zheng
article en

Abstract

The nexin-dynein regulatory complex (N-DRC) is an essential axonemal structure for ciliary and flagellar motility. Coiled-coil domain containing 153 (CCDC153) has recently been identified as a new N-DRC component in Tetrahymena thermophila. However, the physiological function of its mammalian homolog remains unknown. Here, we generated a Ccdc153 knockout mouse model and explored its functional association with motile cilia. We found that CCDC153 was highly expressed in the motile cilia-abundant tissues and localized to the axonemal lumen in motile cilia. However, Ccdc153 knockout mice were viable and exhibited normal brain ventricles and fertility. Overall, our results suggest that CCDC153 is dispensable for ciliary motility in brain ventricles and sperm movement, indicating that CCDC153 is not a potential causative gene in human ciliopathies.

Cytoskeleton
Shandong Normal University (CN)
Openalex Percentile: Top 70%
Genetic and Kidney Cyst Diseases
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The New Nexin‐Dynein Regulatory Complex Component <scp>CCDC153</scp> Is Dispensable for Ciliary Motility and Fertility in Mice — Huijie Zhao, Xunshuo Liu, et al. · Cytoskeleton (2025) | TGRS Research Map | TGRS