March 12, 2020

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Researchers map structure of key chromatin-remodeling complex

Credit: Northwestern University
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Credit: Northwestern University

Northwestern University researchers have mapped a group of proteins that play a critical role in both gene expression and repairing damaged DNA. By understanding this protein complex, called SWI/SNF, researchers hope to better understand how cancer arises.

SWI/SNF regulates the of chromatin, which comprises genetic material in a cell's nucleus and often mutates as cancer develops.

"Mutations of this essential complex have been found in more than 20 percent of all associated with a wide range of tissue types," said Northwestern's Yuan He, who led the study. "Understanding the molecular mechanism of the SWI/SNF complex in regulating chromatin structure and gene transcription is thereby essential for a complete understanding of how chromatin structure alterations lead to cancer."

The paper was published today in the journal Nature. Yuan He is an assistant professor of molecular biosciences in Northwestern's Weinberg College of Arts and Sciences.

To determine the unique structure, the He lab used (cryo-EM), a powerful technique capable of revealing the 3-D shape of large complexes. The technique involves flash-freezing proteins at a speed where water molecules don't have time to re-organize to form crystalline ice. These protein complexes are then directly imaged by an , and their 3-D shape can then be reconstructed in 3-D using a supercomputing cluster. Before cryo-EM, researchers mainly used X-ray crystallography, which is incapable of capturing high-resolution images of important complexes such as this.

This landmark study is the first time that researchers have used cryo-EM to determine the SWI/SNF structure bound to a nucleosome, at near-atomic resolution. "cryo-EM is a revolutionary technique," said Carole LaBonne, chair of the Department of Molecular Biosciences. "It is taking over in the critical field of structural biology. Every major research university is making major investments in this field because it is clear that it holds the key to unraveling many unanswered questions in biomedical science."

Professor Yuan He explained that the structure will allow researchers to map and rationalize cancer-related mutations in the human SWI/SNF complex.

He added that the study will provide the molecular platform for better understanding the important functions of SWI/SNF in both healthy and cancerous states, as well as for developing potential therapeutic strategies for human malignancies.

"Our study gives insight into how the complex suppresses tumor development," He said. "And it could contribute to developing therapeutics for cancers harboring mutations in genes encoding the SWI/SNF complex."

More information: Yan Han et al. Cryo-EM structure of SWI/SNF complex bound to a nucleosome, Nature (2020). DOI: 10.1038/s41586-020-2087-1

Journal information: Nature

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