2003 - 2006  Institute of Physics，Ph.D in condensed matter physics

2006 - 2007  Institute of Chemistry，Post-doctoral research associate

2007 - 2009  Institute of Physics，Assistant Research Professor

2009 - 2023  Institute of Physics，Associate Research Professor

2023 -           Institute of Biophysics，Professor、Principal Investigator

From DNA to chromosomes, there are multiple levels of assembly, including nucleosomes, chromatin fibers, and chromatin loops. High-resolution analysis of dynamic changes in chromatin structure during the reading, replication, and maintenance of genetic information is crucial for quantitatively describing the mechanisms by which various regulatory factors affect chromatin. It is also a key bridge connecting chromatin structure and function. Precise analysis of the interactions and dynamics between biological macromolecules is an advantage of single-molecule manipulation technology, opening a new window for quantitatively describing the epigenetic regulatory mechanisms of chromatin higher-order structures. Our research group has made a series of advances in the dynamic assembly mechanism of tetra-nucleosome units in chromatin fibers, histone chaperone FACT, histone ubiquitination modification, and chromatin remodeling factor SWR1. In the future, our research group will develop various single-molecule characterization techniques to construct a panoramic view of the dynamic structure and regulation of higher-order chromatin structures such as nucleosomes and chromatin fibers, and to understand the molecular mechanisms of diseases caused by chromatin mis-assembly. At the same time, our research group will develop techniques for real-time manipulation of chromatin in vivo to track the dynamics of key life activities such as DNA replication and gene transcription.

1. Anfeng Luo^#, Jingwei Kong^#, Jun Chen^#, Xue Xiao^#, Jie Lan, Xiaorong Li, Cuifang Liu, Peng-Ye Wang, Guohong Li, Wei Li* and Ping Chen*. H2B ubiquitination recruits FACT to maintain a stable altered nucleosome state for transcriptional activation. Nature Communications, 2023, 14: 741.

2. Yi-Zhou Wang^#, Cuifang Liu^#, Jicheng Zhao^#, Juan Yu, Anfeng Luo, Xue Xiao, Shuo-Xing Dou, Lu Ma, Peng-Ye Wang, Ming Li, Guohong Li, Jianbin Yan*, Ping Chen* and Wei Li*. H2A mono-ubiquitination differentiates FACT's functions in nucleosome assembly and disassembly, Nucleic Acids Research, 2022, 50: 833-846.

3. Linchang Dai^#, Xue Xiao^#, Lu Pan, Liuxin Shi, Ning Xu, Zhuqiang Zhang, Xiaoli Feng, Lu Ma, Shuoxing Dou, Pengye Wang, Bing Zhu, Wei Li*, and Zheng Zhou*. Recognition of the Inherently Unstable H2A nucleosome by Swc2 Is a Major Determinant for Unidirectional H2A.Z Exchange, Cell Reports, 2021, 35: 109183.

4. Shuming Zhang, Xue Xiao, Jingwei Kong, Ke Lu, Shuo-Xing Dou, Peng-Ye Wang, Lu Ma, Yuru Liu, Guohong Li, Wei Li*, and Huidong Zhang*. DNA polymerase Gp90 activities and regulations on strand displacement DNA synthesis revealed at single-molecule level, The FASEB Journal, 2021,35(5): e21607.

5. Ping Chen^#, Wei Li^# and Guohong Li*. Structures and Functions of Chromatin Fibers, Annual Review of Biophysics, 2021, 50(1): 95-116

6. Xue Xiao^#; Cuifang Liu^#; Yingxin Pei^#; Yi-Zhou Wang; Jingwei Kong; Ke Lu; Lu Ma; Shuo-Xing Dou; Peng-Ye Wang; Guohong Li; Ping Chen*; Wei Li*. Histone H2A Ubiquitination Reinforces Mechanical Stability and Asymmetry at the Single-Nucleosome Level, Journal of the American Chemical Society, 2020, 142: 3340-3345.

7. Ping Chen^#; Liping Dong^#; Mingli Hu; Yi-Zhou Wang; Xue Xiao; Zhongliang Zhao; Jie Yan; Peng-Ye Wang; Danny Reinberg; Ming Li*; Wei Li*; Guohong Li*. Functions of FACT in Breaking the Nucleosome and Maintaining Its Integrity at the Single-Nucleosome Level, Molecular Cell, 2018, 71: 284-293.

8. Wei Li^#, Ping Chen^#, Juan Yu, Liping Dong, Dan Liang, Jianxun Feng, Jie Yan, Peng-Ye Wang, Qing Li, Zhiguo Zhang, Guohong Li*. FACT Remodels the Tetranucleosomal Unit of Chromatin Fibers for Gene Transcription, Molecular Cell, 2016, 64(1): 120-133

(From Wei Li, July 11, 2023)