Loss of Cep72 affects the morphology of spermatozoa in mice

The centrosome regulates mammalian meiosis by affecting recombination, synapsis, chromosome segregation, and spermiogenesis. Cep72 is one of the critical components of the centrosome. However, the physiological role of Cep72 in spermatogenesis and fertility remains unclear. In this study, we identif...

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Main Authors: Zhen Chen, Yating Xu, Dupeng Ma, Changrong Li, Ziqi Yu, Cong Liu, Tingyu Jin, Ziye Du, Zejia Li, Qi Sun, Yumin Xu, Rong Liu, Yuerong Wu, Mengcheng Luo
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-10-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphys.2022.948965/full
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author Zhen Chen
Yating Xu
Dupeng Ma
Changrong Li
Ziqi Yu
Cong Liu
Tingyu Jin
Ziye Du
Zejia Li
Qi Sun
Yumin Xu
Rong Liu
Yuerong Wu
Mengcheng Luo
author_facet Zhen Chen
Yating Xu
Dupeng Ma
Changrong Li
Ziqi Yu
Cong Liu
Tingyu Jin
Ziye Du
Zejia Li
Qi Sun
Yumin Xu
Rong Liu
Yuerong Wu
Mengcheng Luo
author_sort Zhen Chen
collection DOAJ
description The centrosome regulates mammalian meiosis by affecting recombination, synapsis, chromosome segregation, and spermiogenesis. Cep72 is one of the critical components of the centrosome. However, the physiological role of Cep72 in spermatogenesis and fertility remains unclear. In this study, we identify Cep72 as a testis-specific expression protein. Although Cep72 knockout mice were viable and fertile, their sperms were morphologically abnormal with incomplete flagellum structures. Transcriptome analysis reveals significant differences in six genes (Gm49527, Hbb-bt, Hba-a2, Rps27a-ps2, Gm29647, and Gm8430), which were not previously associated with spermatogenesis. Overall, these results indicate that Cep72 participates in regulating sperm morphology and yet is dispensable for fertility in mice.
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spelling doaj.art-4d2b1cd1ebd64348bdbd599f51e3a3482022-12-22T03:38:09ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2022-10-011310.3389/fphys.2022.948965948965Loss of Cep72 affects the morphology of spermatozoa in miceZhen Chen0Yating Xu1Dupeng Ma2Changrong Li3Ziqi Yu4Cong Liu5Tingyu Jin6Ziye Du7Zejia Li8Qi Sun9Yumin Xu10Rong Liu11Yuerong Wu12Mengcheng Luo13Hubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaCenter for Animal Experiment, Wuhan University, Wuhan, ChinaHubei Provincial Key Laboratory of Developmentally Originated Disease, TaiKang Medical School (School of Basic Medical Sciences), Wuhan University, Wuhan, ChinaThe centrosome regulates mammalian meiosis by affecting recombination, synapsis, chromosome segregation, and spermiogenesis. Cep72 is one of the critical components of the centrosome. However, the physiological role of Cep72 in spermatogenesis and fertility remains unclear. In this study, we identify Cep72 as a testis-specific expression protein. Although Cep72 knockout mice were viable and fertile, their sperms were morphologically abnormal with incomplete flagellum structures. Transcriptome analysis reveals significant differences in six genes (Gm49527, Hbb-bt, Hba-a2, Rps27a-ps2, Gm29647, and Gm8430), which were not previously associated with spermatogenesis. Overall, these results indicate that Cep72 participates in regulating sperm morphology and yet is dispensable for fertility in mice.https://www.frontiersin.org/articles/10.3389/fphys.2022.948965/fullCep72centrosomespermiogenesisfertilitysperm flagellum
spellingShingle Zhen Chen
Yating Xu
Dupeng Ma
Changrong Li
Ziqi Yu
Cong Liu
Tingyu Jin
Ziye Du
Zejia Li
Qi Sun
Yumin Xu
Rong Liu
Yuerong Wu
Mengcheng Luo
Loss of Cep72 affects the morphology of spermatozoa in mice
Frontiers in Physiology
Cep72
centrosome
spermiogenesis
fertility
sperm flagellum
title Loss of Cep72 affects the morphology of spermatozoa in mice
title_full Loss of Cep72 affects the morphology of spermatozoa in mice
title_fullStr Loss of Cep72 affects the morphology of spermatozoa in mice
title_full_unstemmed Loss of Cep72 affects the morphology of spermatozoa in mice
title_short Loss of Cep72 affects the morphology of spermatozoa in mice
title_sort loss of cep72 affects the morphology of spermatozoa in mice
topic Cep72
centrosome
spermiogenesis
fertility
sperm flagellum
url https://www.frontiersin.org/articles/10.3389/fphys.2022.948965/full
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