一、基本信息
姓名:谢海华
职称:教授、博士生导师
联系邮箱:xiehh2025@smu.edu.cn
二、学习经历
2011.9-2015.6 浙江科技大学,生物工程,学士
2015.9-2018.6 温州医科大学,生物学,硕士
2019.9-2024.12 浙江大学,细胞生物学,博士
三、主要研究方向
1. DNA损伤修复通路的动态调控网络与基因组稳定性维持;
2. 复制压力响应网络与基因组稳定性维持;
3. 肿瘤耐药性产生的分子机制与靶向干预策略。
四、代表性论文
1. Xie, H. H.#, Song, L. Z.#, Mao, G. X., Han, J. H., Pu, J. L., Wu, Z. B., Chen, J., Zhou, J. W., Huang, J., Fang, D., and Liu, T. Synergistic protection of nascent DNA at stalled forks by MSANTD4 and BRCA1/2–RAD51, Nature Chemical Biology, 2025.
2. Song, L. Z.#, Xie, H. H.#, Fan, H. N.#, Zhang, Y. J.#, Cheng, Z. X.#, Chen, J. L.#, Guo, Y. Z., Zhang, S. D., Zhou, X. Y., Li, Z. S., Liao, H. X., Han, J. H., Huang, J., Zhou, J. W., Fang, D., and Liu, T. Dynamic control of RNA-DNA hybrid formation orchestrates DNA2 activation at stalled forks by RNAPII and DDX39A, Molecular Cell, 2025, 85(3): 506-522.
3. Xu, Z. Q.#, Xie, H. H.#, Song, L. Z.#, Huang, Y. H., and Huang, J. BRCA1 and BRCA2 in DNA Damage and Replication Stress Response: Insights into Their Functions, Mechanisms, and Implications for Cancer Treatment, DNA Repair, 2025, 150: 103847.
4. Xie, H. H.#, Ge, X. L.#, Yang, F. Y., Wang, B., Li, S., Duan, J. Z., Lv, X. J., Cheng, C. S., Song, Z. M., Liu, C. B., Zhao, J. Z., Zhang, Y., Wu, J. Y., Gao, C. X., Zhang, J. W., and Gu, F. High-fidelity SaCas9 identified by directional screening in human cells, PLOS Biology, 2020, 18(7): e3000747.
5. Xie, H. H., Tang, L. C., He, X. B., Liu, X. X., Zhou, C. C., Liu, J. J., Ge, X. L., Li, J., Liu, C. B., Zhao, J. Z., Qu, J., Song Z. M., and Gu F. SaCas9 Requires 5'-NNGRRT-3' PAM for Sufficient Cleavage and Possesses Higher Cleavage Activity than SpCas9 or FnCpf1 in Human Cells, Biotechnology Journal, 2018, 13(4): e1700561.