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Volume 47 Issue 11
Nov.  2020
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Novel compound heterozygous variants in dynein axonemal heavy chain 17 cause asthenoteratospermia with sperm flagellar defects

doi: 10.1016/j.jgg.2020.07.004
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  • These authors contributed equally to this work.
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  • [1]
    Baker, M.A., Naumovski, N., Hetherington, L., Weinberg, A., Velkov, T., Aitken, R.J., 2013. Head and flagella subcompartmental proteomic analysis of human spermatozoa. Proteomics 13, 61-74.
    [2]
    Coutton, C., Escoffier, J., Martinez, G., Arnoult, C., Ray, P.F., 2015. Teratozoospermia: spotlight on the main genetic actors in the human. Hum. Reprod. Update 21, 455-485.
    [3]
    Hetz, C., Chevet, E., Harding, H. P., 2013. Targeting the unfolded protein response in disease. Nat. Rev. Drug Discov. 12, 703-719.
    [4]
    Houseley, J., Tollervey, D. 2009. The many pathways of RNA degradation. Cell 136, 763-776.
    [5]
    Ishikawa, T., 2017. Axoneme structure from motile cilia. Cold Spring Harbor Perspect. Biol. 9.
    [6]
    Liu, C., Lv, M., He, X., Zhu, Y., Amiri-Yekta, A., Li, W., Wu, H., Kherraf, Z.E., Liu, W., Zhang, J., Tan, Q., Tang, S., Zhu, Y.J., Zhong, Y., Li, C., Tian, S., Zhang, Z., Jin, L., Ray, P., Zhang, F., Cao, Y., 2020. Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility. J. Med. Genet. 57, 31-37.
    [7]
    Loges, N.T., Olbrich, H., Fenske, L., Mussaffi, H., Horvath, J., Fliegauf, M., Kuhl, H., Baktai, G., Peterffy, E., Chodhari, R., Chung, E.M., Rutman, A., O'Callaghan, C., Blau, H., Tiszlavicz, L., Voelkel, K., Witt, M., Zietkiewicz, E., Neesen, J., Reinhardt, R., Mitchison, H.M., Omran, H., 2008. DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm. Am. J. Hum. Genet. 83, 547-558.
    [8]
    Nasr-Esfahani, M.H., Razavi, S., Javdan, Z., Tavalaee, M., 2008. Artificial oocyte activation in severe teratozoospermia undergoing intracytoplasmic sperm injection. Fertil. Steril. 90, 2231-2237.
    [9]
    Nicastro, D., Schwartz, C., Pierson, J., Gaudette, R., Porter, M.E., McIntosh, J.R., 2006. The molecular architecture of axonemes revealed by cryoelectron tomography. Science 313, 944-948.
    [10]
    Rutkowski, D.T., Hegde, R.S., 2010. Regulation of basal cellular physiology by the homeostatic unfolded protein response. J. Cell Biol. 189, 783-794.
    [11]
    Sha, Y.W., Xu, X., Mei, L.B., Li, P., Su, Z.Y., He, X.Q., Li, L., 2017. A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF). Gene 633, 48-53.
    [12]
    Sha, Y.W., Wang, X., Xu, X., Su, Z.Y., Cui, Y., Mei, L.B., Huang, X.J., Chen, J., He, X.M., Ji, Z.Y., Bao, H., Yang, X., Li, P., Li, L., 2019. Novel mutations in CFAP44 and CFAP43 cause multiple morphological abnormalities of the sperm flagella (MMAF). Reprod. Sci. 26, 26-34.
    [13]
    Stoecklin, G., Muhlemann, O. 2013. RNA decay mechanisms: specificity through diversity. Biochim. Biophys. Acta 1829, 487-490.
    [14]
    Walter, P., & Ron, D. 2011. The unfolded protein response: from stress pathway to homeostatic regulation. Science (New York, N.Y.) 334, 1081-1086.
    [15]
    Wambergue, C., Zouari, R., Fourati Ben Mustapha, S., Martinez, G., Devillard, F., Hennebicq, S., Satre, V., Brouillet, S., Halouani, L., Marrakchi, O., Makni, M., Latrous, H., Kharouf, M., Amblard, F., Arnoult, C., Ray, P.F., Coutton, C., 2016. Patients with multiple morphological abnormalities of the sperm flagella due to DNAH1 mutations have a good prognosis following intracytoplasmic sperm injection. Hum. Reprod. 31, 1164-1172.
    [16]
    Wang, S., Kaufman, R.J., 2012. The impact of the unfolded protein response on human disease. J. Cell Biol. 197, 857-867.
    [17]
    Wang, W.L., Tu, C.F., Tan, Y.Q., 2020. Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new? Asian J. Androl. 22, 236-245.
    [18]
    Whitfield, M., Thomas, L., Bequignon, E., Schmitt, A., Stouvenel, L., Montantin, G., Tissier, S., Duquesnoy, P., Copin, B., Chantot, S., Dastot, F., Faucon, C., Barbotin, A.L., Loyens, A., Siffroi, J.P., Papon, J.F., Escudier, E., Amselem, S., Mitchell, V., Toure, A., Legendre, M., 2019. Mutations in DNAH17, encoding a sperm-specific axonemal outer dynein arm heavy chain, cause isolated male infertility due to asthenozoospermia. American J. Hum. Genet.105, 198-212.
    [19]
    Yang, S.M., Li, H.B., Wang, J.X., Shi, Y.C., Cheng, H.B., Wang, W., Li, H., Hou, J.Q., Wen, D.G., 2015. Morphological characteristics and initial genetic study of multiple morphological anomalies of the flagella in China. Asian J. Androl. 17, 513-515.
    [20]
    Zhang, B., Ma, H., Khan, T., Ma, A., Li, T., Zhang, H., Gao, J., Zhou, J., Li, Y., Yu, C., Bao, J., Ali, A., Murtaza, G., Yin, H., Gao, Q., Jiang, X., Zhang, F., Liu, C., Khan, I., Zubair, M., Hussain, H.M.J., Khan, R., Yousaf, A., Yuan, L., Lu, Y., Xu, X., Wang, Y., Tao, Q., Hao, Q., Fang, H., Cheng, H., Zhang, Y., Shi, Q., 2020. A DNAH17 missense variant causes flagella destabilization and asthenozoospermia. J. Exp. Med. 217, e20182365.
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