Discovery Could Aid Search for Huntington’s, Spinocerebellar Ataxia, and Kennedy Disease Treatments
JUPITER, FL, January 17, 2012 – Scientists from the Florida campus of The Scripps Research Institute have identified a compound that can help repair a specific type of defect in RNA, a type of genetic material. The methods in the new study could accelerate the development of therapeutics to treat a variety of incurable diseases such as Huntington’s disease, Spinocerebellar ataxia, and Kennedy disease.
The new study, published January 17, 2012 in an advance, online edition of the journal ACS Chemical Biology, describes a method to find compounds that target defective RNAs, specifically RNA that carries a structural motif known as an “expanded triplet repeat.” The triplet repeat, a series of three nucleotides repeated many more times than normal in the genetic code of affected individuals, has been associated with a variety of neurological and neuromuscular disorders.
“For a long time it was thought that only the protein translated from this type of RNA was toxic,” said Matthew Disney, an associate professor at Scripps Florida who led the new study. “But it has been shown recently that both the protein and the RNA are toxic. Our discovery of a small molecule that binds to RNA and shuts off its toxicity not only further demonstrates that the RNA is toxic but also opens up new avenues for therapeutic development because we have clearly demonstrated that small molecules can reverse this type of defect.”
In the new research, the scientists used a query molecule called 4', 6-diamidino-2-phenylindole (DAPI) as a chemical and structural template to find similar but more active compounds to inhibit a toxic CAG triplet repeat. One of these compounds was then found effective in inhibiting the RNS toxicity of the repeat in patient-derived cells, which demonstrated an improvement in early-stage abnormalities.
“The toxic RNA defect actually sucks up other proteins that play critical roles in RNA processing, and that is what contributes to these various diseases,” Disney said. “Our new compound targets the toxic RNA and inhibits protein binding, shutting off the toxicity. Since the development of drugs that target RNA is extremely challenging, these studies can open up new avenues to exploit RNA drug targets that cause a host of other RNA-mediated diseases.”
Disney and his colleagues are already hard at work to extend the lab’s findings.
The lead author of the study, “Chemical Correction of Pre-mRNA Splicing Defects Associated with Sequestration of Muscleblind-Like 1 Protein by Expanded r(CAG)-containing Transcripts,” is Amit Kumar of Scripps Research. Other authors include Raman Parkesh and Jessica Childs-Disney of Scripps Research, and Lukasz J. Sznajder and Krzysztof Sobczak of Adam Mickiewicz University, Poland. For more information, see http://pubs.acs.org/doi/abs/10.1021/cb200413a
The study was supported by the National Institutes of Health and the Polish Ministry of Science and Higher Education, Camille & Henry Dreyfus Foundation, and the Research Corporation for Science Advancement.
About The Scripps Research Institute
The Scripps Research Institute is one of the world's largest independent, non-profit biomedical research organizations. Scripps Research is internationally recognized for its discoveries in immunology, molecular and cellular biology, chemistry, neuroscience, and vaccine development, as well as for its insights into autoimmune, cardiovascular, and infectious disease. Headquartered in La Jolla, California, the institute also includes a campus in Jupiter, Florida, where scientists focus on drug discovery and technology development in addition to basic biomedical science. Scripps Research currently employs about 3,000 scientists, staff, postdoctoral fellows, and graduate students on its two campuses. The institute's graduate program, which awards Ph.D. degrees in biology and chemistry, is ranked among the top ten such programs in the nation. For more information, see www.scripps.edu.
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For information:
Eric Sauter
Tel: 215-862-2689
erics165@comcast.net
Mika Ono
Tel: 858-784-2052
Fax: 858-784-8136
mikaono@scripps.edu
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