
曾虎
北京大学未来技术学院研究员
生命科学联合中心PI
实验室主页:https://zenghupku.github.io/
电子邮件: huzeng(AT)pku.edu.cn;
研究领域:
基因在特定时间和空间的表达决定细胞的功能和命运,我们实验室致力于建立具有空间、时间和单细胞分辨的测序技术,并应用这些测序技术在时空维度探究基因表达调控和疾病致病机理。具体包括:
1. 开发空间多组学技术;
2. 解析基因表达调控网络;
3. 探究神经系统疾病致病机理。
研究兴趣:
实验室聚焦基因在时空维度上的表达调控及其在疾病中的作用。主要方向包括:开发具有空间、时间和单细胞分辨率的多组学测序技术,实现转录组、翻译组等在同一组织样本中的高通量原位联合检测;利用这些时空多组学数据揭示基因表达在不同调控维度的相互作用,解析基因表达调控网络;将方法学与疾病研究结合,重点研究神经退行性疾病与脑肿瘤,解析基因表达时空异常如何驱动病理表型,并寻找潜在治疗靶点。通过技术开发与生物学问题并重,旨在构建从分子机制到临床转化的研究路径,推动时空组学在基础与转化医学中的应用。
代表性科研成果:
1. J Ren#, H Zeng#, J Huang#, J Tian, M Wu, H Shi, X Sui, C K Wang, H Zhou, Z Tang, S Luo, X Wang*. Spatially resolved in situ profiling of mRNA life cycle at transcriptome scale in intact cells and tissues using STARmap PLUS, RIBOmap and TEMPOmap. Nat. Protoc. (2026) 21, 1629–1661.
2. T Hui#, J Zhou#, M Yao, Y Xie, H Zeng*. Advances in spatial omics technologies. Small Methods (2025), e2401171. (Review)
3. H Zeng#, J Huang#, J Ren#, C K Wang, Z Tang, H Zhou, Y Zhou, H Shi, A Aditham, X Sui, H Chen, J A Lo, X Wang*. Spatially Resolved single-cell translatomics at molecular resolution. Science (2023) 380, eadd3067. (Highlighted in the Nature Reviews Genetics and Nature Methods).
4. J Ren#, H Zhou#, H Zeng#, C K Wang, J Huang, X Qiu, X Sui, Q Li, X Wu, Z Lin, J A Lo, K Maher, Y He, X Tang, J Lam, H Chen, B Li, D E Fisher, J Liu, X Wang*. Spatiotemporally resolved transcriptomics reveals the subcellular RNA kinetic landscape. Nat. Methods (2023) 20, 695–705.
5. H Zeng#, J Huang#, H Zhou#, W J. Meilandt, B Dejanovic, Y Zhou, C J. Bohlen, S Lee, J Ren, A Liu, Z Tang, H Sheng, J Liu, M Sheng*, X Wang*. Integrative in situ mapping of single-cell transcriptional states and tissue histopathology in a mouse model of Alzheimer's disease. Nat. Neurosci. (2023) 26, 430–446.
6. H Zeng#, M Mondal#, R Song#, J Zhang, B Xia, M Liu, C Zhu, B He, YQ Gao* and C Yi*. Unnatural cytosine bases recognized as thymines by DNA polymerases via the formation of the Watson-Crick geometry. Angew. Chem. Int. Ed. (2019) 58, 130-133.
7. H Zeng#, B He#, C Yi*. Compilation of modern technologies to map genome-wide cytosine modifications in DNA. Chembiochem (2019) 20, 1898-1905. (Review)
8. H Zeng#, B He#, B Xia, D Bai, X Lu, J Cai, L Chen, A Zhou, C Zhu, H Meng, Y Gao, H Guo, C He*, Q Dai*, and C Yi*. Bisulfite-Free, Nanoscale Analysis of 5-Hydroxymethylcytosine at Single Base Resolution. J. Am. Chem. Soc. (2018) 140, 13190-13194.
9. H Zeng#, B He#, C Yi*, and J Peng*. Liquid biopsies: DNA methylation analyses in circulating cell-free DNA. J. Genet. Genomics (2018) 45, 185-192. (Review)