06:35am Tuesday 21 November 2017

Researchers Uncover Therapeutic Strategy for Ultra-Rare Genetic Disease

Using a laboratory model involving fruit flies, genetic researchers at the University of Miami Miller School of Medicine have identified a metabolic problem that may be responsible for Snyder-Robinson syndrome (SRS), an ultra-rare disorder that affects only boys.

“Our findings indicate that an anti-oxidative therapy may be helpful in combating the symptoms of SRS, including delays in speech, lack of energy and other developmental problems,” said R. Grace Zhai, Ph.D., associate professor of molecular and cellular pharmacology. “We have been working closely with the Snyder-Robinson Foundation for several years, and our findings have guided parents in seeking treatment for their sons with SRS. Many have reported significant improvements in their sons’ physical, speech and cognitive functions from this metabolic therapy.”

Zhai added that the SRS study shows the power of a combined approach using Drosophila (fruit fly) models in the laboratory and human patient cells for cross-validation and immediate translation. “This combined approach could provide ways to expedite the discovery of potential treatment strategies for rare neurological diseases, which are difficult to study in traditional clinical trials,” said Zhai, who is the senior author of the study published November 2 in the journal Nature Communications.

Chong Li, a graduate student in Zhai’s laboratory, was first author of the SRS study, “Spermine Synthase Deficiency Causes Lysosomal Dysfunction and Oxidative Stress in Models of Snyder-Robinson Syndrome.” Miller School co-authors were graduate students Jennifer M. Brazill and Yi Zhu, and research associates Christofer Bello and Zoraida Diaz-Perez. The international collaborative study involved the National Institutes of Health Undiagnosed Diseases Program (NIHUDP), Yantai University in China, and Greenwood Genetic Center in South Carolina.

“Currently there are 31 individuals with confirmed diagnosis all over the world,” Li said. “However, the number has been growing steadily with the advancement in diagnosis. It is a devastating disease with no treatments, even though it has been half a century since the first case was reported.”

SRS is an X-linked genetic disorder characterized by intellectual disability and developmental delays that affect speech, mobility, and cognition. Many boys with SRS are thin and have low muscle mass and skeletal problems, particularly osteoporosis. Neurological problems are common, including seizures that begin in childhood. SRS may also present additional health challenges, such as kidney or respiratory issues.

Zhai’s research team found that SRS is caused by mutations in spermine synthase (SMS), a polyamine enzyme that is essential for life. With SRS, the mutations generate toxic metabolites, including aldehydes and reactive oxygen species, which subsequently impairs the autophagy-lysosome pathway and puts oxidative stress on cells and causes other metabolic problems. “The oxidative stress caused by loss of SMS is suppressed by genetically or pharmacologically enhanced antioxidant activity,” Li said.

Zhai has been studying rare neurological disorders for nearly a decade, with current support from the NIH, which collects patient DNA and provides genetic data to researchers. “In about 50 percent of these disorders, the NIHUDPhas identified a potential mutation in the genome, but can’t determine if it is causing the disease or not,” she said.

In 2013, Zhai received a grant from NIHUDP for a pilot project using fruit flies to screen these mutant genes identified in UDP to learn which variations might be harmful to cellular functions. Next, they modeled those mutations and compared the outcomes with cells from patient skin samples.

“It was very rewarding for us, as laboratory scientists, to be able to meet families facing the challenges of SRS,” Zhai said. ‘By sharing our results we could point them in the right direction for therapy.”

 

Miller School of Medicine

 


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