E3 ligase FBXO22 is not significant for spermatogenesis and male fertility in mice

被引:5
作者
Wu, Tiantian [1 ]
Jin, Xin [2 ]
Huang, Chao [3 ]
Yu, Xiangling [4 ]
Xu, Bingya [4 ]
Gao, Wenxin [1 ]
Qiu, Xiya [3 ]
Bao, Mingyuan [1 ]
Zhao, Dan [5 ]
Feng, Guannan [2 ]
Zheng, Bo [3 ,6 ]
Huang, Xiaoyan [1 ,7 ]
机构
[1] Nanjing Med Univ, Sch Basic Med Sci, Dept Histol & Embryol, State Key Lab Reprod Med & Offspring Hlth, Nanjing 211166, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Suzhou Municipal Hosp, Affiliated Suzhou Hosp, Dept Obstet & Gynecol,Gusu Sch, Suzhou 215002, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Suzhou Hosp, Suzhou Municipal Hosp, Ctr Reprod & Genet,State Key Lab Reprod Med & Offs, Suzhou 215002, Jiangsu, Peoples R China
[4] Jiangnan Univ, Human Reprod & Genet Ctr, Affiliated Hosp, Wuxi 214122, Jiangsu, Peoples R China
[5] Jiangsu Univ, Affiliated Hosp 4, Zhenjiang 212008, Jiangsu, Peoples R China
[6] Nanjing Med Univ, Affiliated Suzhou Hosp, Suzhou Municipal Hosp, Ctr Reprod & Genet,State Key Lab Reprod Med,Gusu S, Suzhou 215002, Jiangsu, Peoples R China
[7] Nanjing Med Univ, Sch Basic Med Sci, Dept Histol & Embryol, State Key Lab Reprod Med, Nanjing 211166, Jiangsu, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2024年 / 16卷 / 05期
基金
中国国家自然科学基金;
关键词
Fbxo22; spermatogenesis; knockout; male fertility; UBIQUITIN; PROTEIN;
D O I
10.62347/STDA4237
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: F -box -only protein 22 (FBXO22), an important substrate receptor of the SKP1-Cullin-F-box (SCF) ubiquitin ligases, has been reported to be involved in many biological processes, including tumorigenesis, neurological disorders, cellular senescence, and DNA damage. However, the specific role of FBXO22 during spermatogenesis is poorly understood. Methods: We produced Fbxo22 conditional knockout (cKO) and global knockout (KO) mice and assessed their sperm masurements using a computer -assisted sperm analysis (CASA) system. Additionally, we conducted histologic staining and immunostaining to examine the impact of Fbxo22 loss on spermatogenesis. Results: Our results revealed that there were no notable differences in semen quality, fertility test results, or histologic findings in Fbxo22 -KO and Fbxo22 -cKO mice compared to the control group. Conclusions: Our study demonstrated that Fbxo22 is not significant for spermatogenesis or male fertility in mice. These findings will help researchers avoid redundant efforts and serve as a foundational resource for genetic studies on human fertility.
引用
收藏
页数:12
相关论文
共 28 条
[1]  
Arama E, 2007, PLOS BIOL, V5, P2745, DOI 10.1371/journal.pbio.0050251
[2]   A Conserved F Box Regulatory Complex Controls Proteasome Activity in Drosophila [J].
Bader, Maya ;
Benjamin, Sigi ;
Wapinski, Orly L. ;
Smith, David M. ;
Goldberg, Alfred L. ;
Steller, Hermann .
CELL, 2011, 145 (03) :371-382
[3]   A novel F-box protein is required for caspase activation during cellular remodeling in Drosophila [J].
Bader, Maya ;
Arama, Eli ;
Steller, Hermann .
DEVELOPMENT, 2010, 137 (10) :1679-1688
[4]   Ubiquitin-Proteasome System in Spermatogenesis [J].
Bose, Rohini ;
Manku, Gurpreet ;
Culty, Martine ;
Wing, Simon S. .
POSTTRANSLATIONAL PROTEIN MODIFICATIONS IN THE REPRODUCTIVE SYSTEM, 2014, 759 :181-213
[5]   Fbxw17 is dispensable for viability and fertility in mice [J].
Chen, Zhen ;
Ma, Dupeng ;
Jin, Tingyu ;
Yu, Ziqi ;
Li, Jiong ;
Sun, Qi ;
Li, Zejia ;
Du, Ziye ;
Liu, Rong ;
Li, Yi ;
Luo, Mengcheng .
MOLECULAR BIOLOGY REPORTS, 2022, 49 (08) :7287-7295
[6]   Emerging role of FBXO22 in carcinogenesis [J].
Cheng, Jiangting ;
Lin, Min ;
Chu, Man ;
Gong, Longyuan ;
Bi, Yanli ;
Zhao, Yongchao .
CELL DEATH DISCOVERY, 2020, 6 (01)
[7]   FBXO47 regulates telomere-inner nuclear envelope integration by stabilizing TRF2 during meiosis [J].
Hua, Rong ;
Wei, Huafang ;
Liu, Chao ;
Zhang, Yue ;
Liu, Siyu ;
Guo, Yueshuai ;
Cui, Yiqiang ;
Zhang, Xin ;
Guo, Xuejiang ;
Li, Wei ;
Liu, Mingxi .
NUCLEIC ACIDS RESEARCH, 2019, 47 (22) :11755-11770
[8]   FBXO22, an epigenetic multiplayer coordinating senescence, hormone signaling, and metastasis [J].
Johmura, Yoshikazu ;
Harris, Alexsander ;
Ohta, Tomohiko ;
Nakanishi, Makoto .
CANCER SCIENCE, 2020, 111 (08) :2718-2725
[9]   FBXO22 inhibits proliferation and metastasis of cervical cancer cells by mediating ubiquitination-dependent degradation of GAK [J].
Li, Shanfeng ;
Shi, Lei ;
Wang, You ;
Zhang, Lanxia ;
Chu, Sufang ;
Li, Minle ;
Bai, Jin ;
Zhu, Weipei .
EXPERIMENTAL CELL RESEARCH, 2023, 430 (01)
[10]   Fbxo22 inhibits metastasis in triple-negative breast cancer through ubiquitin modification of KDM5A and regulation of H3K4me3 demethylation [J].
Li, Siqiaozhi ;
He, Jinsong ;
Liao, Xin ;
He, Yixuan ;
Chen, Rui ;
Chen, Junhui ;
Hu, Sean ;
Sun, Jia .
CELL BIOLOGY AND TOXICOLOGY, 2023, 39 (04) :1641-1655