兼职教师
赵世民

  教授,国家重大科学研究计划首席科学家

  电话:021-31246779

  邮箱:zhaosm@fudan.edu.cn

  地址:上海市杨浦区湾谷科技园2期D3座1409室  


个人简介

国家重大科学研究计划首席科学家,基金委“创新群体”负责人,科技部重点领域创新团队负责人,上海市优秀学术带头人,上海市领军人才。1984-1988年就读北京师范大学化学系,1988-1995在中国医学科学院从事研究工作,2000年获美国Purdue大学生物化学博士学位。2000-2005年分别在美国宝洁(P&G)等公司任职,2006年至今历任任复旦大学副研究员/教授,博士导师。现任复旦大学代谢与整合生物学研究院副院长,生命科学院教授,生物医学研究院高级PI,遗传工程国家重点实验室PI,国家蛋白质重大研究计划首席科学家。进行代谢与疾病,蛋白质翻译后修饰与蛋白组学等研究工作。

主要研究方向

主要从事代谢物的感知与信号传导、代谢物信号失调的致病机理等相关研究。用生物化学、分子生物学、蛋白组学和生物信息学等手段, 研究代谢调控机理及代谢失调与人类疾病发生的关系。重点研究:1.代谢酶的修饰失调导致的人类疾病发病机理及其新的干预手段;2. 代谢中间体失调导致肿瘤的发生机理及干预手段。近年来承担了国家重大科学研究计划、国自然重点项目、国家科技合作项目、上海市基础研究项目等多项研究。迄今,在Science、Cancer Cell、Molecular Cell、Cell Metabolism、Circulation等国际重要学术刊物发表论文。实验室网站:http://metabolism.fudan.edu.cn/

荣誉及获奖情况

  • 2017年   中华医学科技奖二等奖,中华医学会

  • 2016年   科技部创新人才推进计划“重点领域创新团队”负责人,科技部

  • 2016年   上海医学科技奖二等奖,上海市医学会

  • 2015年   上海领军人才,上海市委组织部

  • 2013年   自然科学一等奖,教育部

  • 2013年   上海市优秀学术带头人,上海市科委

  • 2013年  “药明康德生命化学研究奖”学者奖,药明康德公司

  • 2012年    第一届校园科技新星,上海市政府

  • 2011年  “中国科学十大进展”,科技部

  • 2010年  “中国高等学校十大科技进展”,教育部

  • 2010年   谈家桢生命科学创新奖,上海市生物医药协会/科技部

  • 2010年   明治乳业生命科学研究杰出奖,国家人类基因组南方研究中心

代表性成果

  1. Mei XY, Qi DS, Zhang T, Zhao Y, Jin L, Hou JL, Wang JH, Lin Y, Xue Y, Zhu PP, Liu ZX, Huang L, Nie J, Si W, Ma JY, Ye JH, Finnell R H, Saiyin H, Wang HY, Zhao JY, Zhao SM, Xu W. Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects. EMBO Molecular Medicine, 2020, e9469. doi: 10.15252/emmm.201809469.

  2. Qu YY, Zhao R, Zhang HL, Zhou Q, Xu FJ, Zhang X, Xu WH, Shao N, Zhou SX, Dai B, Zhu Y, Shi GH, Shen YJ, Zhu YP, Han CT, Chang K, Lin Y, Zang WD, Xu W, Ye DW, Zhao SM, Zhao JY. Inactivation of the AMPK-GATA3-ECHS1 pathway induces fatty acid synthesis that promotes clear cell renal cell carcinoma growth. Cancer Research, 2020, 80(2): 319-333.

  3. Yang Li, Cui-Fang Yao, Fu-Jiang Xu, Yuan-Yuan Qu, Jia-Tao Li, Yan Lin, Zhong-Lian Cao, Peng-Cheng Lin, Wei Xu, Shi-Min Zhao*, Jian-Yuan Zhao*. APC/CCDH1 synchronizes ribose-5-phosphate levels and DNA synthesis to cell cycle progression. Nature communications,2019, 10: 2502.

  4. Qin Zhang, Baoling Bai, Xinyu Mei, Chunlei Wan, Haiyan Cao, Dan Li, Shan Wang, Min Zhang ,Zhigang Wang , Jianxin Wu, Hongyan Wang, Junsheng Huo, Gangqiang Ding, Jianyuan Zhao, Qiu Xie,Li Wang , Zhiyong Qiu*, Shiming Zhao*, Ting Zhang*. Elevated H3K79 homocysteinylation causes abnormal gene expression during neural development and subsequent neural tube defects. Nature communications, 2018, 9: 3436.

  5. Xia-Di He, Wei Gong, Jia-Nong Zhang, Ji Nie, Cui-Fang Yao, Fu-Shen Guo, Yan Lin, Xiao-Hui Wu, Feng Li, Jie Li, Wei-Cheng Sun, En-Duo Wang, Yan-Peng An, Hui-Ru Tang, Guo-Quan Yan, Peng-Yuan Yang, Yun Wei, Yun-Zi Mao, Peng-Cheng Lin, Jian-Yuan Zhao, Yanhui Xu*, Wei Xu*, Shi-Min Zhao*. Sensing and Transmitting Intracellular Amino Acid Signals through Reversible Lysine Aminoacylations. Cell Metabolism, 2018, 27: 1-16.

  6. Ya-Kun Zhang, Yuan-Yuan Qu, Yan Lin, Xiao-Hui Wu, Hou-Zao Chen, Xu Wang, Kai-Qiang Zhou,Yun Wei, Fushen Guo, Cui-Fang Yao, Xia-Di He, Li-Xia Liu, Chen Yang, Zong-Yuan Guan, Shi-Dong Wang, Jianyuan Zhao, De-Pei Liu*, Shi-Min Zhao*, Wei Xu*. Enoyl-CoA hydratase-1 regulates mTOR signaling and apoptosis by sensing nutrients. Nature communications, 2017, 8: 464.

  7. Dan Wang, Feng Wang, Kai-Hu Shi, Hui Tao, Yang Li, Rui Zhao, Han Lu, Wenyuan Duan, Bin Qiao, Shi-Min Zhao*, Hongyan Wang*, Jian-Yuan Zhao*. Lower Circulating Folate Induced by a Fidgetin Intronic Variant Is Associated With Reduced Congenital Heart Disease Susceptibility. Circulation,2017, 135: 1733-1748.

  8. Li, F., He, X., Ye, D., Lin, Y., Yu, H., Yao, C., Huang, L., Zhang, J., Wang, F., Xu, S., Wu, X., Liu, L., Yang, C., Shi, J., He, X., Liu, J., Qu, Y., Guo, F., Zhao, J., Xu, W., and Zhao, S*. NADP(+)-IDH Mutations Promote Hypersuccinylation that Impairs Mitochondria Respiration and Induces Apoptosis Resistance. Molecular cell, 2015, 60: 661-675.

  9. Wenqing Jiang, Shiwen Wang, Mengtao Xiao,Yan Lin, Lisha Zhou, Qunying Lei,Yue Xiong,Kun-Liang Guan, Shimin Zhao*.  Acetylation regulates gluconeogenesis by promoting PEPCK1 degradation via recruiting the UBR5 ubiquitin ligase. Molecular Cell, 2011, 43: 1-12.

  10. Xu W, Yang H, Liu Y, Yang Y, Wang P, Kim S, Ito S, Yang C, Wang P, Xiao M, Liu L, Jiang W, Liu J, Zhang J, Wang B, Frye S, Zhang Y, Xu Y, Lei Q, Guan K, Zhao S*, Y. Xiong. Oncometabolite 2-hydroxyglutarate is a competitive inhibitor of α- ketoglutarate-dependent dioxygenases. Cancer Cell, 2011, 19: 17-30.

  11. Qijun Wang, Yakun Zhang, Hui Xiong,Yan Lin, Hong Li, Lu Xie, Wei Zhao, YufengYao, Yue Xiong, Kun-Liang Guan, Shimin Zhao*, Guo-Ping Zhao. Acetylation of Metabolic Enzymes Coordinates Carbon Source Utilization and Metabolic Flux. Science, 2010, 327: 1004-1008.

  12. Shimin Zhao, Wei Xu, Wenqing Jiang, Wei Yu, Yan Lin, Tengfei Zhang,Jun Yao, Pengyuan Yang, Hong Li, Yixue Li, Jiong Shi, Lunxiu Qin, Qunying Lei, Yue Xiong and Kun-Liang Guan. Regulation of Cellular Metabolism by Protein Lysine Acetylation. Science, 2010, 327: 1000-1004.

  13. Shimin Zhao, Yan Lin, Wei Xu, Wenqing Jiang, Zhengyu Zha, Pu Wang,Wei Yu,Zhiqiang Li, Lingling Gong, Yingjie Peng, Jianping Ding, Qunying Lei, Kun-Liang Guan, Yue Xiong. Glioma-Derived Mutations in IDH1Dominantly Inhibit IDH1 Catalytic Activity and Induce HIF-1a. Science, 2009, 324: 261-265.