副教授

陈嘉瑜

姓名:陈嘉瑜
学位:博士
导师情况:博士生导师
研究领域:干细胞与细胞重编程
研究方向:1. 细胞命运转变过程中的表观遗传调控机制研究
          2. 基于CRISPR/Cas9基因编辑技术的疾病模型构建的研究
E-mail: chenjiayu@tongji.edu.cn
联系电话:021-65987363
实验室网址:http://life.tongji.edu.cn/gaolab/

招生要求:热爱科研、有团队意识、有责任感、不怕困难

 

个人简历:
2017.12-至今     同济大学生命科学与技术学院,副教授
2014.10-2017.11     同济大学生命科学与技术学院,助理教授
2014.2-2014.10     同济大学转化医学高等研究院,助理研究员
2009.9-2014.1      北京协和医学院,北京生命科学研究所,生物化学与分子生物学博士
2004.9-2009.6      复旦大学,上海医学院,医学学士
 

研究方向简介:
       陈嘉瑜博士是同济大学生命科学与技术学院,高绍荣课题组的副教授,国际干细胞协会会员。陈嘉瑜博士主要进行细胞命运转变过程中的表观遗传调控机制研究,以及基于CRISPR/Cas9基因编辑技术的疾病模型构建的研究。陈嘉瑜博士的代表性工作是首次证明了DNA羟甲基化酶Tet1可通过其羟甲基化活性,加速多能基因调控区域的去甲基化进程,激活多能性基因的表达,从而促进细胞多能性的建立,提高诱导型重编程的速率和效率,证实Tet1可取代部分Yamanaka转录因子建立高质量的iPS细胞系,并高效地产生足月的、健康的、完全由iPS细胞发育而来的all-iPSC小鼠。该项成果在Cell Stem Cell杂志以封面研究发表,并被评为年度最佳论文之一。此外,陈嘉瑜博士以主要骨干身份参与科技部“国家重点研发计划干细胞及转化研究重点专项”及“国家重大科学研究计划(973)”各一项,结题国家自然科学基金“青年项目”一项。陈嘉瑜博士也已参与国内外多个课题研究工作,在Cell Stem Cell,Nature,Nature Cell biology,Molecular Cell 等国际知名学术期刊发表相关成果20余篇,其中第一作者或通讯作者论文共8篇。

发表论文

    1. He W#, Zhang X#, Zhang Y, Zheng W, Xiong Z, Hu X, Wang M, Zhang L, Zhao K, Qiao Z, Lai W, Lv C, Kou X, Zhao Y, Yin J, Liu W, Jiang Y, Chen M, Xu R, Le R, Li C, Wang H, Wan X, Wang H, Han Z, Jiang C*, Gao S*, Chen J*. Reduced Self-Diploidization and Improved Survival of Semi-cloned Mice Produced from Androgenetic Haploid Embryonic Stem Cells through Overexpression of Dnmt3b. Stem Cell Reports. 2018 Jan 26. pii: S2213-6711(18)30001-8. doi: 10.1016/j.stemcr.2017.12.024. (*Co-correspondence)
    2. Liu W#, Bai D#, Chen J*, Gao S*. Additive-effect pattern of both ZP2 and ZP3 in human and mouse. Hum Genet. 2017 Nov 1. doi: 10.1007/s00439-017-1848-x. (*Co-correspondence)
    3. Liu W#, Li K#, Bai D#, Yin J#, Tang Y, Chi F, Zhang L, Wang Y, Pan J, Liang S, Guo Y, Ruan J, Kou X, Zhao Y, Wang H, Chen J*, Teng X*, Gao S*. Dosage effects of ZP2 and ZP3 heterozygous mutations cause human infertility. Hum Genet. 2017 Aug;136(8):975-985. doi: 10.1007/s00439-017-1822-7. Epub 2017 Jun 24. (*Co-correspondence)
    4. Gao R#, Xiu W#, Zhang L, Zang R, Yang L, Wang C, Wang M, Wang M, Yi L, Tang Y, Gao Y, Wang H, Xi J, Liu W, Wang Y, Wen X, Yu Y, Zhang Y, Chen L*, Chen J*, Gao S*. Direct induction of neural progenitor cells transiently passes through a partially reprogrammed state. Biomaterials. 2017 Mar;119:53-67. doi: 10.1016/j.biomaterials.2016.12.007. (*Co-correspondence)
    5. Xu K#, Chen X#, Yang H, Xu Y, He Y, Wang C, Huang H, Liu B, Liu W, Li J, Kou X, Zhao Y, Zhao K, Zhang L, Hou Z, Wang H, Wang H, Li J, Fan H, Wang F, Gao Y, Zhang Y, Chen J*, Gao S*. Maternal Sall4 Is Indispensable for Epigenetic Maturation of Mouse Oocytes. J Biol Chem. 2017 Feb 3;292(5):1798-1807. doi: 10.1074/jbc.M116.767061. Epub 2016 Dec 28. (*Co-correspondence)
    6. Chen J#*, Gao Y#, Huang H, Xu K, Chen X, Jiang Y, Li H, Gao S, Tao Y, Wang H, Zhang Y, Wang H, Cai T, Gao S*. The combination of Tet1 with Oct4 generates high-quality mouse induced pluripotent stem cells (iPSCs). Stem Cells. 2015 Mar;33(3):686-98. doi: 10.1002/stem.1879. (#co-first authors, *Co-correspondence)
    7. Liu X#, Chen J#, Liu W, Li X, Chen Q, Liu T, Gao S*, Deng M*. The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation. Neurogenetics. 2015 Jul;16(3):223-31. doi: 10.1007/s10048-015-0448-y. Epub 2015 Apr 26. (#co-first authors)
    8. Gao Y#, Chen J#, Li K, Wu T, Huang B, Liu W, Kou X, Zhang Y, Huang H, Jiang Y, Yao C, Liu X, Lu Z, Xu Z, Kang L, Chen J, Wang H, Cai T and Gao S (2013). Replacement of Oct4 by Tet1 during iPSC induction reveals an important role of DNA methylation and hydroxymethylation in reprogramming. Cell Stem Cell, 12(4):453-469, 2013. (Cover Story; Previewed by Cell Stem Cell; Selected as Best of 2013 by Cell Stem Cell) (#co-first authors)
    9. Zhuang Q, Li W, Benda C, Huang Z, Ahmed T, Liu P, Guo X, Ibañez DP, Luo Z, Zhang M, Abdul MM, Yang Z, Yang J, Huang Y, Zhang H, Huang D, Zhou J, Zhong X, Zhu X, Fu X, Fan W, Liu Y, Xu Y, Ward C, Khan MJ, Kanwal S, Mirza B, Tortorella MD, Tse HF, Chen J, Qin B, Bao X, Gao S, Hutchins AP, Esteban MA. NCoR/SMRT co-repressors cooperate with c-MYC to create an epigenetic barrier to somatic cell reprogramming. Nat Cell Biol. 2018 Mar 12. doi: 10.1038/s41556-018-0047-x.
    10. Zhu J, Wang K, Li T, Chen J, Xie D, Chang X, Yao J, Wu J, Zhou Q, Jia Y, Duan T. Hypoxia-induced TET1 facilitates trophoblast cell migration and invasion through HIF1α signaling pathway. Sci Rep. 2017 Aug 14;7(1):8077. doi: 10.1038/s41598-017-07560-7.
    11. Li Y, Hai Y, Chen J, Liu T. Differentiating Chondrocytes from Peripheral Blood-derived Human Induced Pluripotent Stem Cells. J Vis Exp. 2017 Jul 18;(125). doi: 10.3791/55722.
    12. Li H, Lai P, Jia J, Song Y, Xia Q, Huang K, He N, Ping W, Chen J, Yang Z, Li J, Yao M, Dong X, Zhao J, Hou C, Esteban MA, Gao S, Pei D, Hutchins AP, Yao H. RNA Helicase DDX5 Inhibits Reprogramming to Pluripotency by miRNA-Based Repression of RYBP and its PRC1-Dependent and -Independent Functions. Cell Stem Cell. 2017 Jan 11. pii: S1934-5909(16)30458-1. doi: 10.1016/j.stem.2016.12.002.
    13. Liu X, Wang C, Liu W, Li J, Li C, Kou X, Chen J, Zhao Y, Gao H, Wang H, Zhang Y, Gao Y, Gao S (2016). Distinct features of H3K4me3 and H3K27me3 chromatin domains in pre-implantation embryos. Nature. 2016 Sep 14;537(7621):558-562. doi: 10.1038/nature19362.
    14. Xiong J, Zhang Z, Chen J, Huang H, Xu Y, Ding X, Zheng Y, Nishinakamura R, Xu G, Wang H, Chen S, Gao S and Zhu B (2016). Cooperative Action between SALL4A and TET Proteins in Stepwise Oxidation of 5-Methylcytosine. Molecular Cell, http://dx.doi.org/10.1016/j.molcel.2016.10.013.
    15. Zhang W, Xia W, Wang Q, Towers AJ, Chen J, Gao R, Zhang Y, Yen CA, Lee AY, Li Y, Zhou C, Liu K, Zhang J, Gu TP, Chen X, Chang Z, Leung D, Gao S, Jiang YH, Xie W. (2016). Isoform Switch of TET1 Regulates DNA Demethylation and Mouse Development. Molecular Cell. http://dx.doi.org/10.1016/j.molcel.2016.10.030.
    16. Xiong Z, Yi L, Cao D, He W, Chen J, Gao S, Sun X (2016). Dravet syndrome with autism inherited from a paternal mosaic heterozygous mutation on SCN1A. J Neurol Sci. 2016 Oct 15;369:53-6. doi: 10.1016/j.jns.2016.07.038.
    17. Li, Y., T. Liu, N. Van Halm-Lutterodt, J. Chen, Q. Su and Y. Hai (2016). "Reprogramming of blood cells into induced pluripotent stem cells as a new cell source for cartilage repair." Stem Cell Res Ther 7(1): 31.
    18. Illich, D. J., M. Zhang, A. Ursu, R. Osorno, K. P. Kim, J. Yoon, M. J. Arauzo-Bravo, G. Wu, D. Esch, D. Sabour, D. Colby, K. S. Grassme, J. Chen, B. Greber, S. Hoing, W. Herzog, S. Ziegler, I. Chambers, S. Gao, H. Waldmann and H. R. Scholer (2016). "Distinct Signaling Requirements for the Establishment of ESC Pluripotency in Late-Stage EpiSCs." Cell Rep. 2016 Apr 14. pii: S2211-1247(16)30362-X. doi: 10.1016/j.celrep.2016.03.073.
    19. Xu, S., X. Zhu, H. Li, Y. Hu, J. Zhou, D. He, Y. Feng, L. Lu, G. Du, Y. Hu, T. Liu, Z. Wang, G. Ding, J. Chen, S. Gao, F. Wu, Z. Xue, Y. Li and G. Fan (2016). "The 14th Ile residue is essential for Leptin function in regulating energy homeostasis in rat." Sci Rep. 2016 Jul 5;6:28508. doi: 10.1038/srep28508.
    20. Yang, Y., X. Zhang, L. Yi, Z. Hou, J. Chen, X. Kou, Y. Zhao, H. Wang, X. F. Sun, C. Jiang, Y. Wang and S. Gao (2016). Naive Induced Pluripotent Stem Cells Generated From beta-Thalassemia Fibroblasts Allow Efficient Gene Correction With CRISPR/Cas9. Stem Cells Transl Med 5(2): 267.
    21. Wei, T., W. Chen, X. Wang, M. Zhang, J. Chen, S. Zhu, L. Chen, D. Yang, G. Wang, W. Jia, Y. Yu, T. Duan, M. Wu, H. Liu, S. Gao and J. Kang (2015). An HDAC2-TET1 switch at distinct chromatin regions significantly promotes the maturation of pre-iPS to iPS cells. Nucleic Acids Res doi:10.1093/nar/gkv430.
    22. Liu X, Chen J, Li X, Gao S, Deng M. (2014) Generation of induced pluripotent stem cells from amyotrophic lateral sclerosis patient carrying SOD1-V14M mutation. Natl Med J China, DOI:10.3760/cma.j.issn.0376-2491. 2014.27.017.
    23. Chang G, Gao S, Hou X, Xu Z, Liu Y, Kang L, Tao Y, Liu W, Huang B, Kou X, Chen J, An L, Miao K, Di K, Wang Z, Tan K, Cheng T, Cai T, Gao S*, Tian J*. (2013) High-throughput sequencing reveals the disruption of methylation of imprinted gene in induced pluripotent stem cells. Cell Research, doi:10.1038/cr.2013.173.
    24. Jiao J, Yang Y, Shi Y, Chen J, Gao R, Fan Y, Yao H, Liao W, Sun X* and Gao S*. (2013) Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons. Human Molecular Genetics, 22(21):4241-4252.
    25. Wang Y, Zheng C, Jiang Y, Zhang J, Chen J, Yao C, Zhao Q, Liu S, Chen K, Du J, Yang Z, Gao S*. (2012) Genetic correction of β-thalassemia patient-specific iPS cells and its use in improving hemoglobin production in irradiated SCID mice. Cell Research, 22(4):637-48.
    26. Yang P, Wang Y, Chen J, Li H, Kang L, Zhang Y, Chen S, Zhu B*, Gao S*. (2011) Rcor2 is a Subunit of the LSD1 Complex that Regulates ES Cell Property and Substitutes for Sox2 in Reprogramming Somatic Cells to Pluripotency. Stem Cells, 29(5):791-801.
    27. Cai X, Zhang J, Chen M, Wu Y, Wang X, Chen J, Zhang J, Shen X, Qu D, Jiang H.(2011) The effect of the potential PhoQ histidine kinase inhibitors on Shigella flexneri virulence. PLoS One, 6(8):e23100, 2011.
    28. 陈嘉瑜, 蔡霞, 瞿涤; 沙门菌PhoP-PhoQ双组分信号转导系统[J]; 微生物与感染; 201004.

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