Volume 43 Issue 2
Mar.  2022
Turn off MathJax
Article Contents
Wei Liu, Yue-Wen Wang, Huan Zhang, Xue-Feng Xie, Ao Ma, Qumar Zaman, Abdul Rafay Javed, Tanveer Abbas, Wasim Shah, Riaz Ahmad, Da-Ren Zhao, Hui Ma, Muhammad Zubair, Ranjha Khan, Qing-Hua Shi. Computationally predicted pathogenic USP9X mutation identified in infertile men does not affect spermatogenesis in mice. Zoological Research, 2022, 43(2): 225-228. doi: 10.24272/j.issn.2095-8137.2021.409
Citation: Wei Liu, Yue-Wen Wang, Huan Zhang, Xue-Feng Xie, Ao Ma, Qumar Zaman, Abdul Rafay Javed, Tanveer Abbas, Wasim Shah, Riaz Ahmad, Da-Ren Zhao, Hui Ma, Muhammad Zubair, Ranjha Khan, Qing-Hua Shi. Computationally predicted pathogenic USP9X mutation identified in infertile men does not affect spermatogenesis in mice. Zoological Research, 2022, 43(2): 225-228. doi: 10.24272/j.issn.2095-8137.2021.409

Computationally predicted pathogenic USP9X mutation identified in infertile men does not affect spermatogenesis in mice

doi: 10.24272/j.issn.2095-8137.2021.409
Funds:  This study was supported by the Fundamental Research Funds for the Central Universities (WK2070080005)
More Information
  • Corresponding author: E-mail: ranjha@ustc.edu.cnqshi@ustc.edu.cn
  • Received Date: 2021-12-25
  • Accepted Date: 2022-01-25
  • Published Online: 2022-01-25
  • Publish Date: 2022-03-18
  • loading
  • [1]
    Djureinovic D, Fagerberg L, Hallström B, Danielsson A, Lindskog C, Uhlén M, et al. 2014. The human testis-specific proteome defined by transcriptomics and antibody-based profiling. Molecular Human Reproduction, 20(6): 476−488. doi: 10.1093/molehr/gau018
    [2]
    Ernst C, Eling N, Martinez-Jimenez CP, Marioni JC, Odom DT. 2019. Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis. Nature Communications, 10(1): 1251. doi: 10.1038/s41467-019-09182-1
    [3]
    Farhi J, Ben-Haroush A. 2011. Distribution of causes of infertility in patients attending primary fertility clinics in Israel. Israel Medical Association Journal, 13(1): 51−54.
    [4]
    Gershoni M, Hauser R, Barda S, Lehavi O, Arama E, Pietrokovski S, et al. 2019. A new MEIOB mutation is a recurrent cause for azoospermia and testicular meiotic arrest. Human Reproduction, 34(4): 666−671. doi: 10.1093/humrep/dez016
    [5]
    Guerri G, Maniscalchi T, Barati S, Busetto GM, Del Giudice F, De Berardinis E, et al. 2019. Non-syndromic monogenic male infertility. Acta Biomedica, 90(10-S): 62−67.
    [6]
    Guo JT, Grow EJ, Mlcochova H, Maher GJ, Lindskog C, Nie XC, et al. 2018. The adult human testis transcriptional cell atlas. Cell Research, 28(12): 1141−1157. doi: 10.1038/s41422-018-0099-2
    [7]
    Kishi K, Uchida A, Takase HM, Suzuki H, Kurohmaru M, Tsunekawa N, et al. 2017. Spermatogonial deubiquitinase USP9X is essential for proper spermatogenesis in mice. Reproduction, 154(2): 135−143. doi: 10.1530/REP-17-0184
    [8]
    Okutman O, Rhouma MB, Benkhalifa M, Muller J, Viville S. 2018. Genetic evaluation of patients with non-syndromic male infertility. Journal of Assisted Reproduction and Genetics, 35(11): 1939−1951. doi: 10.1007/s10815-018-1301-7
    [9]
    Rimoin DL, Connor JM, Pyeritz RE, Korf BR. 2007. Emery and Rimoin's Principles and Practice of Medical Genetics. 5th ed. Philadelphia: Churchill Livingstone Elsevier.
    [10]
    Singh P, Schimenti JC. 2015. The genetics of human infertility by functional interrogation of SNPs in mice. Proceedings of the National Academy of Sciences of the United States of America, 112(33): 10431−10436. doi: 10.1073/pnas.1506974112
    [11]
    Sironen A, Shoemark A, Patel M, Loebinger MR, Mitchison HM. 2020. Sperm defects in primary ciliary dyskinesia and related causes of male infertility. Cellular and Molecular Life Sciences, 77(11): 2029−2048. doi: 10.1007/s00018-019-03389-7
    [12]
    Stegeman S, Jolly LA, Premarathne S, Gecz J, Richards LJ, Mackay-Sim A, et al. 2013. Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis. PLoS One, 8(7): e68287. doi: 10.1371/journal.pone.0068287
    [13]
    Wang K, Li MY, Hakonarson H. 2010. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Research, 38(16): e164. doi: 10.1093/nar/gkq603
    [14]
    Zhang YW, Zhong LW, Xu B, Yang YF, Ban RJ, Zhu J, et al. 2013. SpermatogenesisOnline 1.0: a resource for spermatogenesis based on manual literature curation and genome-wide data mining. Nucleic Acids Research, 41(D1): D1055−D1062. doi: 10.1093/nar/gks1186
  • ZR-2021-409 Supplementary Materials.pdf
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(1)

    Article Metrics

    Article views (699) PDF downloads(145) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return