留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos

Yubing Liu Xinmei Lu Min Ye Ling Wang Rongxin Tang Zhiyong Yang Bongkoch Turathum Chenchen Liu Yujing Xue Menghua Wu Yannan Yang Ermeng Gao Di Zhang Feng Yang Keh-Kooi Kee Xingxu Huang Guanglei Li Ri-Cheng Chian

Yubing Liu, Xinmei Lu, Min Ye, Ling Wang, Rongxin Tang, Zhiyong Yang, Bongkoch Turathum, Chenchen Liu, Yujing Xue, Menghua Wu, Yannan Yang, Ermeng Gao, Di Zhang, Feng Yang, Keh-Kooi Kee, Xingxu Huang, Guanglei Li, Ri-Cheng Chian. Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos[J]. 遗传学报, 2022, 49(10): 982-985. doi: 10.1016/j.jgg.2022.02.010
引用本文: Yubing Liu, Xinmei Lu, Min Ye, Ling Wang, Rongxin Tang, Zhiyong Yang, Bongkoch Turathum, Chenchen Liu, Yujing Xue, Menghua Wu, Yannan Yang, Ermeng Gao, Di Zhang, Feng Yang, Keh-Kooi Kee, Xingxu Huang, Guanglei Li, Ri-Cheng Chian. Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos[J]. 遗传学报, 2022, 49(10): 982-985. doi: 10.1016/j.jgg.2022.02.010
Yubing Liu, Xinmei Lu, Min Ye, Ling Wang, Rongxin Tang, Zhiyong Yang, Bongkoch Turathum, Chenchen Liu, Yujing Xue, Menghua Wu, Yannan Yang, Ermeng Gao, Di Zhang, Feng Yang, Keh-Kooi Kee, Xingxu Huang, Guanglei Li, Ri-Cheng Chian. Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos[J]. Journal of Genetics and Genomics, 2022, 49(10): 982-985. doi: 10.1016/j.jgg.2022.02.010
Citation: Yubing Liu, Xinmei Lu, Min Ye, Ling Wang, Rongxin Tang, Zhiyong Yang, Bongkoch Turathum, Chenchen Liu, Yujing Xue, Menghua Wu, Yannan Yang, Ermeng Gao, Di Zhang, Feng Yang, Keh-Kooi Kee, Xingxu Huang, Guanglei Li, Ri-Cheng Chian. Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos[J]. Journal of Genetics and Genomics, 2022, 49(10): 982-985. doi: 10.1016/j.jgg.2022.02.010

Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos

doi: 10.1016/j.jgg.2022.02.010
基金项目: 

D Program of China (2017YFC1002003), and the project sponsored by the National Natural Science Foundation of China (31601197).

This work was supported by the National Key R&

详细信息
    通讯作者:

    Guanglei Li,E-mail:ligl@shanghaitech.edu.cn

    Ri-Cheng Chian,E-mail:rcchian@tongji.edu.cn

Efficient silencing of the multicopy DUX4 gene by ABE-mediated start codon mutation in human embryos

Funds: 

D Program of China (2017YFC1002003), and the project sponsored by the National Natural Science Foundation of China (31601197).

This work was supported by the National Key R&

  • Adikusuma, F., Williams, N., Grutzner, F., Hughes, J. & Thomas, P., 2017. Targeted deletion of an entire chromosome using CRISPR/Cas9. Mol. Ther. 25, 1736-1738
    Chen, Z. & Zhang, Y., 2019. Loss of DUX causes minor defects in zygotic genome activation and is compatible with mouse development. Nat. Genet. 51, 947-951
    De Iaco, A., Planet, E., Coluccio, A., Verp, S., Duc J & Trono, D., 2017. DUX-family transcription factors regulate zygotic genome activation in placental mammals. Nat. Genet. 49, 941-945
    Gaudelli, N. M., Komor, A. C., Rees, H. A., Packer, M. S., Badran, A. H., Bryson, D. I. & Liu, D. R., 2017. Programmable base editing of A*T to G*C in genomic DNA without DNA cleavage. Nature. 551, 464-471
    Guo, M., Zhang, Y., Zhou, J., Bi, Y., Xu, J., Xu, C., Kou, X., Zhao, Y., Li, Y. & Tu, Z., et al., 2019. Precise temporal regulation of Dux is important for embryo development. Cell Res. 29, 956-959
    Hosseini, E., Mehraein, F., Shahhoseini, M., Karimian, L., Nikmard, F., Ashrafi, M., Afsharian, P. & Aflatoonian, R., 2016. Epigenetic alterations of CYP19A1 gene in Cumulus cells and its relevance to infertility in endometriosis. J. Assist. Reprod. Genet. 33, 1105-1113
    Jin, S., Zong, Y., Gao, Q., Zhu, Z., Wang, Y., Qin, P., Liang, C., Wang, D., Qiu, J. L. & Zhang, F., et al., 2019. Cytosine, but not adenine, base editors induce genome-wide off-target mutations in rice. Science. 364, 292-295
    Komor, A. C., Kim, Y. B., Packer, M. S., Zuris, J. A. & Liu, D. R., 2016. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage. Nature. 533, 420-424
    Kuscu, C., Parlak, M., Tufan, T., Yang, J., Szlachta, K., Wei, X., Mammadov, R. & Adli, M., 2017. CRISPR-STOP:gene silencing through base-editing-induced nonsense mutations. Nat. Methods. 14, 710-712
    A, L. R. & K, N. K., 2019. Human germline genome editing. Nat. Cell Biol. 21, 1479-1489
    Ledford, H., 2020. CRISPR gene editing in human embryos wreaks chromosomal mayhem. Nature. 583, 17-18
    Hendrickson, Peter G., et al., 2017. Conserved roles of mouse DUX and human DUX4 in activating cleavage-stage genes and MERVL/HERVL retrotransposons. Nat. Genet. 49, 925-934
    Rickels, R., Herz, H. M., Sze, C. C., Cao, K., Morgan, M. A., Collings, C. K., Gause, M., Takahashi, Y. H., Wang, L. & Rendleman, E. J., et al., 2017. Histone H3K4 monomethylation catalyzed by Trr and mammalian COMPASS-like proteins at enhancers is dispensable for development and viability. Nat. Genet. 49, 1647-1653
    Sha, Q. Q., Zhang, J. & Fan, H. Y., 2019. A story of birth and death:mRNA translation and clearance at the onset of maternal-to-zygotic transition in mammalsdagger. Biol. Reprod. 101, 579-590
    Sha, Q. Q., Zhu, Y. Z., Li, S., Jiang, Y., Chen, L., Sun, X. H., Shen, L., Ou, X. H. & Fan, H. Y., 2020. Characterization of zygotic genome activation-dependent maternal mRNA clearance in mouse. Nucleic Acids Res. 48, 879-894
    Skeparnias, I., Alphanastasakis, D., Shaukat, A. N., Grafanaki, K. & Stathopoulos, C., 2017. Expanding the repertoire of deadenylases. RNA Biol. 14, 1320-1325
    Snider, L., Asawachaicharn, A., Tyler, A. E., Geng, L. N., Petek, L. M., Maves, L., Miller, D. G., Lemmers, R. J., Winokur, S. T. & Tawil, R., et al., 2009. RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units:new candidates for the pathophysiology of facioscapulohumeral dystrophy. Hum. Mol. Genet. 18, 2414-2430
    Snider, L., Geng, L. N., Lemmers, R. J., Kyba, M., Ware, C. B., Nelson, A. M., Tawil, R., Filippova, G. N., van der Maarel, S. M. & Tapscott, S. J., et al., 2010. Facioscapulohumeral dystrophy:incomplete suppression of a retrotransposed gene. PLoS Genet. 6, e1001181
    Vassena, R., Boue, S., Gonzalez-Roca, E., Aran, B., Auer, H., Veiga, A. & Izpisua, B. J., 2011. Waves of early transcriptional activation and pluripotency program initiation during human preimplantation development. Development. 138, 3699-3709
    Wang, X., Liu, Z., Li, G., Dang, L., Huang, S., He, L., Ma, Y., Li, C., Liu, M. & Yang, G., et al., 2020. Efficient gene silencing by adenine base editor-mediated start codon mutation. Mol. Ther. 28, 431-440
    Whiddon, J. L., Langford, A. T., Wong, C. J., Zhong, J. W. & Tapscott, S. J., 2017. Conservation and innovation in the DUX4-family gene network. Nat. Genet. 49, 935-940
    Wood, K., Tellier, M. & Murphy, S., 2018. DOT1L and H3K79 methylation in transcription and genomic stability. Biomolecules. 8
    Yan, L., Yang, M., Guo, H., Yang, L., Wu, J., Li, R., Liu, P., Lian, Y., Zheng, X. & Yan, J., et al., 2013. Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells. Nat. Struct. Mol. Biol. 20, 1131-1139
    Zeng, Y., Li, J., Li, G., Huang, S., Yu, W., Zhang, Y., Chen, D., Chen, J., Liu, J. & Huang, X., 2018. Correction of the marfan syndrome pathogenic FBN1 mutation by base editing in human cells and heterozygous embryos. Mol. Ther. 26, 2631-2637
    Zhang, M., Zhou, C., Wei, Y., Xu, C., Pan, H., Ying, W., Sun, Y., Sun, Y., Xiao, Q. & Yao, N., et al., 2019. Human cleaving embryos enable robust homozygotic nucleotide substitutions by base editors. Genome Biol. 20, 101
    Zuccaro, Michael V., et al., 2020. Allele-specific chromosome removal after Cas9 cleavage in human embryos. Cell. 183, 1650-1664.e15
    Zuo, E., Sun, Y., Wei, W., Yuan, T., Ying, W., Sun, H., Yuan, L., Steinmetz, L. M., Li, Y. & Yang, H., 2019. Cytosine base editor generates substantial off-target single-nucleotide variants in mouse embryos. Science. 364, 289-292
  • 加载中
计量
  • 文章访问数:  697
  • HTML全文浏览量:  254
  • PDF下载量:  31
  • 被引次数: 0
出版历程
  • 收稿日期:  2021-09-08
  • 录用日期:  2022-02-17
  • 修回日期:  2022-01-26
  • 刊出日期:  2022-02-26

目录

    /

    返回文章
    返回