DUX4 structure unveiled

DUX4 sequence-specific determinants
(A and B) Views of the a3 helices of HD1 (A) and HD2 (B) inserted in the DNA major groove, with the side chains making base-specific contacts and some of the surrounding residues shown in sticks.

MINNEAPOLIS, MN- December 12, 2018 – New research by University of Minnesota scientists has revealed the three-dimensional structure of the DUX4 protein, which is responsible for the disease, facioscapulohumeral muscular dystrophy (FSHD). Unlike the majority of genetic diseases, FSHD is not caused by a protein that is missing or not functioning properly. Rather it is caused when a functioning, normal, protein shows up in a place where it doesn’t belong (in muscles).

In the paper “Crystal structure of the double homeodomain of DUX4 in complex with DNA,” published in the latest issue of the journal Cell Reports, Michael Kyba, Ph.D., professor and Lillehei Endowed Scholar in the University of Minnesota Medical School; and Hideki Aihara, Ph.D., associate professor of Biochemistry, Molecular Biology, and Biophysics in the College of Biological Sciences, crystallized the part of the DUX4 protein that binds to DNA, exposed it to strong X-rays, and used the interference patterns to determine the molecular structure of the protein in three dimensions.

“In many diseases, such structural information has led to the development of drugs to treat those diseases,” explained Kyba, “thus this research is an important step on the path to therapy for FSHD.”

The structural information also revealed important details about how humans are different from other mammals. “Although all eutherian mammals have a protein equivalent to DUX4, the human protein behaves slightly differently from the mouse protein,” says Aihara. “Our structure showed that a single amino acid difference is responsible for this altered behavior. Furthermore, only primates have this amino acid, meaning that the interaction of the DUX4 protein with DNA in humans, apes and monkeys, is slightly different from that in all other mammals.”

By interacting with DNA, the DUX4 protein turns other genes on or off, leading to changes in the function of the cell. Understanding how DUX4 interacts with DNA allows researchers to make predictions about the genes that it regulates and how this causes muscle damage.

Among genetic diseases, FSHD is one of the more common. It is thought to affect close to 1 million people worldwide and currently has no treatment. “Although we have known for many years that DUX4 causes FSHD, we have not had a good explanation for how it damages muscle,” said Kyba. “Seeing for the first time what this protein actually looks like when it binds to DNA, and knowing that this is the act that is responsible for so much suffering, was both remarkable and sobering.”

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This research was funded by the Friends of FSH Research and by the National Institute of General Medical Sciences (NIGMS) and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS).

Reposted from EurekaAlert.

Reference
Lee JK, Bosnakovski D, Toso EA, Dinh T, Banerjee S, Bohl TE, Shi K, Orellana K, Kyba M, Aihara H.Crystal Structure of the Double Homeodomain of DUX4 in Complex with DNA. Cell Rep. 2018 Dec 11;25(11):2955-2962.e3. doi: 10.1016/j.celrep.2018.11.060. PDF of article.

Here is Dr. Aihara and his colleagues in a 2016 video explaining why they wanted to determine the DUX4 structure.

 

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2 responses to “DUX4 structure unveiled”

  1. Wow!! Truly amazing and remarkable how much information and new understanding of FSHD has been published in only the past few years. It seems like every few months the really smart people working on this disease are publishing something not only new and exciting, but really meaningful. Thanks so much to all the great folks out there that make solving FSHD a big part of their career!

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