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Solving a genetic mystery: Bridging diagnostic discovery through social media

Date:
September 10, 2015
Source:
Baylor College of Medicine
Summary:
Scientists describe in a new article how USP7 becomes a 'disease gene.' It begins with the triad of genes -- MAGEL2, TRIM27 and USP7 -- and their effect on the critical process of the recycling of proteins within cells that is regulated by ubiquitination and deubiquitination.
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"Help us find others like Tess." Bo Bigelow's plea jumps off the page of his blog, echoing across the continent from his leafy green home city of Portland, Maine.

When he posted his call to action, all he knew was that his young daughter has a mutation in her USP7 gene and that she has global developmental delay, hip dysplasia and visual impairment caused by her brain (not a problem in her eyes themselves) among other health issues. An article in the New Yorker magazine by Seth Mnookin gave him hope that finding other children with the same mutated gene as his daughter might point the way toward understanding what was causing her problems and even spark the science that could solve.

Unbeknownst to Bigelow, in a laboratory in steamy Houston a young researcher named Dr. Christian Schaaf, an assistant professor of molecular and human genetics at Baylor College of Medicine, was already on the trail of USP7, and he had found seven children with USP7 mutations and symptoms similar to those of Tess. Schaaf sought out Dr. Ryan Potts of the University of Texas Southwestern School of Medicine at Dallas, who had already been studying the gene.

In a report in the journal Molecular Cell, Schaaf, Potts, and their colleagues (including first authors Yi-Heng Hao of UT Southwestern and Michael D. Fountain Jr., of Baylor College of Medicine) describe how USP7 becomes a "disease gene." It begins with the triad of genes -- MAGEL2, TRIM27 and USP7 -- and their effect on the critical process of the recycling of proteins within cells that is regulated by ubiquitination and deubiquitination.

"This process keeps everything in homeostasis," said Schaaf, an assistant professor of molecular and human genetics at Baylor and the Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital. "It makes sure the right proteins are recycled at the right pace. We began to look at USP7 because we realized it interacts closely with MAGEL2. If you lose the protein MAGEL2, it causes Schaaf-Yang syndrome," a disorder discovered by Schaaf and his colleague Dr. Yaping Yang at Baylor that has symptoms similar to those seen in the disorder suffered by Tess and the seven youngsters that Schaaf had located through a search of genome databases.

Proteins associated with USP7, MAGEL2 and TRIM27 form a complex that regulates each other and those downstream of their activity within the cell.

Basically, players in the complex act like a rheostat, fine-tuning the protein recycling pathway.

"It's like the thermostat on an air conditioner that self regulates to keep the temperature constant," said Schaaf. "This process keeps everything in balance. If you lose the function of MAGEL2, the disease called Schaaf-Yang results. If you lose the function of USP7, it may cause a disease that looks very similar -- molecularly and clinically."

After Schaaf had sent his paper in to the journal, students in his lab became aware of Bigelow and his blog that spearheads the search for help for his curly-headed daughter whose USP7 gene is awry.

They have contacted Bigelow, and Tess' data may become part of future studies.

It's a new method of finding patients with mutated genes that is becoming increasingly important in the study of genetics. Driven by technology that makes it possible to determine the sequence of an individual's exome and look for mutations, often by comparing it to the exomes of the two parents, parents and patients often take to social media in order to find answers to their problems. Bigelow hoped his blog and podcasts about Tess, "Stronger Every Day," would draw parents with similar dilemmas to him. As their numbers grow, they can push for research into the problem that affects their children.

"I've taken the strategy of the guy in the New Yorker article," he said. "Let other people find out. It's a reverse beacon that so far has connected us with this study and Dr. Schaaf. I would love to find more people."

"You hear the term 'rare disease,' and I'm not sure it's the best name for it," said Bigelow. "If you look at all the so-called rare diseases, it appears that there may be as many as 39 million people afflicted with them. The idea that you are alone is fading away as we connect with people."


Story Source:

Materials provided by Baylor College of Medicine. Note: Content may be edited for style and length.


Journal Reference:

  1. Yi-Heng Hao, Michael D. Fountain, Klementina Fon Tacer, Fan Xia, Weimin Bi, Sung-Hae L. Kang, Ankita Patel, Jill A. Rosenfeld, Cédric Le Caignec, Bertrand Isidor, Ian D. Krantz, Sarah E. Noon, Jean P. Pfotenhauer, Thomas M. Morgan, Rocio Moran, Robert C. Pedersen, Margarita S. Saenz, Christian P. Schaaf, Patrick Ryan Potts. USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder. Molecular Cell, 2015; DOI: 10.1016/j.molcel.2015.07.033

Cite This Page:

Baylor College of Medicine. "Solving a genetic mystery: Bridging diagnostic discovery through social media." ScienceDaily. ScienceDaily, 10 September 2015. <www.sciencedaily.com/releases/2015/09/150910131803.htm>.
Baylor College of Medicine. (2015, September 10). Solving a genetic mystery: Bridging diagnostic discovery through social media. ScienceDaily. Retrieved May 23, 2017 from www.sciencedaily.com/releases/2015/09/150910131803.htm
Baylor College of Medicine. "Solving a genetic mystery: Bridging diagnostic discovery through social media." ScienceDaily. www.sciencedaily.com/releases/2015/09/150910131803.htm (accessed May 23, 2017).

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