Huntington's Disease (HD) is an inherited disorder that leads to degeneration of neurons in the brain, mental and physical deterioration, and inevitably, the death of afflicted persons. The disease results from mutational expansion of the number of repeats of the trinucleotide CAG in the huntingtin (htt) gene, resulting in production of a defective Htt protein that forms insoluble aggregates in brain cells. Recent investigations have shown that a transcription elongation complex called Supt4/Supt5h is required for the gene-transcribing enzyme RNA polymerase to proceed through expanded lengths of repeats on DNA templates. When the Supt4h/Supt5h complex is reduced, the expanded repeats of mutated genes present an obstacle that leads to dissociation of the polymerase from DNA-prematurely truncating the mutant transcripts, decreasing production of the defective Htt protein, and enabling neurons that contain the abnormal genes to remain viable. The Supt4h/Supt5h complex is needed also for progression of the polymerase through expansions of multinucleotide repeats associated with other dominantly inherited neurodegenerative and neuromuscular diseases (NDs), suggesting that targeting the Supt4h/Supt5h complex may be a broadly applicable approach for treatment of multiple diseases caused by such expansions;these diseases include, in addition to HD, certain muscular dystrophies and spinocerebellar ataxias. The proposed project will identify potential therapies that interfere with Supt4h/5h complex formation and test the hypothesis that expression of genes containing expanded repeats will be reduced by such therapy, while expression of normal genes remain unaffected. It will develop, test, and validate methods for and suitability of luminescence assays that will be used to screen large chemical libraries and computationally designed peptides for agents that block Supt4h binding to its Supt5h partner (i.e., Supt4h/5h interaction inhibitors;SIIs). Using a procedure that distinguishes between transcription of mutant vs. normal copies of repeat-containing genes, the project will quantify the specificity of SII effects on mutant genes in induced pluripotent stem cells (iPSCs) derived from patients afflicted with HD or other NDs, and will determine the influence of the length of expanded repeats on such specificity. Possible consequences of interference with Supt4h/Supt5h complex formation on transcription of genomic loci external to targeted genes will be assessed by high-throughput RNA sequencing methods (RNA-Seq). The National Center for Advancing Translational Sciences (NCATS) at the NIH will collaborate in screening and medicinal chemistry manipulations aimed at developing promising "hits" into therapeutic "leads". Collectively, the results of these experiments are expected to: 1) indicate whether interference with Supt4h/5h complex formation can broadly affect production of abnormal gene products in nucleotide repeat disorders, 2) elucidate the quantitative relationship between repeat length and selectivity of Supt4h/Supt5h complex effects, and 3) identify specific agents and/or molecular groups suitable for further development as therapies for these diseases.

Public Health Relevance

Collectively, the societal burden of Huntington's Disease and other incurable, inherited neurodegenerative and neuromuscular diseases on afflicted persons, their families, and the health care system is very great. Validation of the hypothesis that these diseases are amenable to a uniform therapeutic approach and confirmation of the Supt4h/5h protein complex as a target for this approach would establish a new paradigm for research on, and treatment of, these horrific diseases.

Agency
National Institute of Health (NIH)
Type
Research Project (R01)
Project #
5R01NS085812-02
Application #
8742023
Study Section
Special Emphasis Panel (ZNS1)
Program Officer
Sutherland, Margaret L
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Stanford University
Department
Genetics
Type
Schools of Medicine
DUNS #
City
Stanford
State
CA
Country
United States
Zip Code
94304