Zhucheng CHEN    Ph.D.

Professor


1994-1998       B.S., NanKai University            

1998-2001       M.S., Peking University            

2001-2003      M.S., New York University            

2003-2008      Ph.D., Cornell University                

2008-2011       Postdoc, UT Southwestern Medical Center

2011-2017        Tenure-track associate Professor, School of Life Sciences, Tsinghua University

2017-2020      Tenured associate Professor, School of Life Sciences, Tsinghua University

2020-             Professor, School of Life Sciences, Tsinghua University    

 

Research interest


DNA is tightly wrapped around histones to form nucleosomes, the basic repeating unit of chromatin and the material basis of epigenetics. However, the assembly of nucleosomes and the formation of compact chromatin impede the reading of genetic information encoded in DNA. Epigenetic mechanisms, such as DNA methylation, histone modifications, nucleosome positioning, and heterochromatin architecture, are critical for decoding genetic information and play essential roles in gene transcription, cell fate determination, and human diseases.

Our laboratory primarily employs biophysical approaches, combined with biochemical and other interdisciplinary methods, to investigate the structure, mechanism, and biological function of chromatin regulators. Our work has captured multiple key states of chromatin remodeling, elucidated the underlying molecular mechanism, and proposed the “DNA wave” model for chromatin remodeling. We have determined high-resolution structures of several SWI/SNF family chromatin remodeling complexes, revealing their mechanisms of assembly and nucleosome recognition, thus providing a framework for understanding the pathogenesis of related mutations. We also discovered the first human chromatin remodeler that specifically recognizes sub-nucleosomal particles.

We aim to provide a structural basis for the precise reading and editing of epigenetic information, deepen our understanding of biological processes such as gene expression regulation and DNA damage repair, and lay an important foundation for the mechanistic study and targeted drug development of related diseases.


Selected publications


1. Hu P#, Sun J#, Sun H#, Chen K#, Sia Y, Xia X, Xi Q*, Chen Z*. Subnucleosome preference of human chromatin remodeler SMARCAD1 Nature, 644(8077):818-826, 2025

2. Sia Y#, Pan H#, Chen K, Chen Z*. Structural insights into chromatin remodeling by ISWI during active ATP hydrolysis Science 388 (6751): eadu5654. 2025

3. Li L#, Chen K#, Sia Y#, Hu P, Ye Y, Chen Z*. Structure of the ISW1a complex bound to the dinucleosome Nat. Struct. Mol. Biol, 31(2):266-274, 2024

4. Qe K#, Chen K#, Wang H#, Li X*, Chen Z*. Structure of the NuA4 acetyltransferase complex bound to the nucleosome Nature, 610(7932):569-574 2022

5. Yuan J#, Chen K#, Zhang W. Chen Z*. Structure of human PBAF chromatin remodeling complex bound to a nucleosome Nature, 605(7908):166-171, 2022

6. Ye Y#, Wu H#, Chen K, Clapier CR, Verma N, Zhang W, Deng H, Cairns BR*, Gao N*Chen Z*. Structure of the RSC complex bound to the nucleosome. Science, 366(6467):838-843, 2019

7. Yan L#, Wu H#, Li X, Gao N*, Chen Z* Structures of the ISWI-nucleosome complex reveal a conserved mechanism of chromatin remodeling Nat. Struct. Mol. Biol. 26(4):258-266, 2019

8. Li M#, Xia X#, Tian Y#, Jia Q#, Liu X#, Ying L, Li M*, Li X*, Chen Z*. Mechanism of DNA translocation underlying chromatin remodeling by Snf2 Nature, 567(7748): 409-413, 2019.

9. Liu X#, Li M#, Xia X#, Li X*, Chen Z*. Mechanism of chromatin remodelling revealed by the Snf2-nucleosome structure Nature 544 (7651):440-445, 2017

10. Yan L#, Wang L#, Tian Y, Xia X, Chen Z*. Structure and regulation of the chromatin remodeller ISWI. Nature 540(7633):466-469, 2016


Contact information


Tel: +86-10-62796096
Website: http://www.chenzclab.com/

E-mail: zhucheng_chen@mail.tsinghua.edu.cn