MECHANISM OF ACTION OF HISTONE DEACETYLASE INHIBITORS ON SURVIVAL MOTOR NEURON 2 PROMOTER

Date
2018-05
Journal Title
Journal ISSN
Volume Title
Publisher
University of Delaware
Abstract
Spinal muscular atrophy (SMA) is an early-onset recessive neurodegenerative disease that primarily affects the α-motor neurons in the anterior horn of the spinal cord. The degeneration of these motor neurons leads to gradual muscular atrophy, eventual respiratory complications, and early death in severe types of SMA. Due to deletion or mutation events, patients with SMA lack a functional copy of the Survival Motor Neuron 1 (SMN1) gene. Humans however have a nearly identical copy of SMN1 known as Survival Motor Neuron 2 (SMN2), which is retained in SMA patients. The major difference between SMN1 and SMN2 is that SMN2 contains a nucleotide substitution in exon 7 that results in the exclusion of this exon in the majority of mRNA transcripts produced from SMN2. This exclusion of exon 7 results in low levels of functional SMN protein. In animal models and within patient populations, it has been shown that increasing SMN2 copy number results in a less severe SMA phenotype, making SMN2 an ideal target for SMA therapeutics. Histone deacetylase (HDAC) inhibitors have been extensively studied for treatment of SMA through increasing transcription of the SMN2 gene; however, several of these HDAC inhibitors demonstrated a highly variable patient response and possible toxicity. In this project, I examine the HDAC inhibitors RGFP106, RGFP109, CAY10433, and HDACi-IV to determine their potential for increasing SMN2 transcription and develop a SMN2 promoter dual luciferase assay for studying the potential mechanism of action of these drug compounds. These compounds were selected to study as they have shown positive effects on SMN2 expression in human SMA fibroblast cell lines. RGFP106 and RGFP109 increased transcription of Smn in NSC-34 motor neuron-like cells. The preliminary test of the SMN2 dual luciferase assay showed that all test compounds activated the SMN2 promoter, but this data was possibly skewed due to concurrent upregulation of the TK promoter control. My drug compounds of interest failed to significantly increase promoter activation in a SMN2 β-lactamase promoter assay. My findings indicate that these HDAC inhibitors may not act on the SMN2 promoter through direct transcription factor based activity, thus an alternative mechanism must be explored.
Description
Keywords
Biological Sciences, Histone deacetlyalse inhibitors, survival motor neuron 2 promoter
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