Cell Systems to Pre-Clinical Models

点击翻译按钮获取中文摘要

PROJECT SUMMARY Knowledge of epilepsy genes has exploded with the advent of next generation DNA sequencing (NGS), yet our understanding of how any specific gene mutation leads to epilepsy increasingly lags behind gene discovery. With the expanding list of potential epilepsy genes comes the problem of genetic variants of uncertain significance (VUS), confounding definitive diagnosis, genetic counselling and treatment strategies. The ultimate goal of the EpiMVP team is to develop a highly integrated and effective multiplatform pipeline to determine the functional impact of VUS for non-ion channel epilepsy genes. To this end, the Gene and Variant Curation Core (GVCC) provides in silico prediction of VUSs to prioritize and refine specific genes and VUS for study as Project 1 (Genes to Proteins) begins in vitro biochemical and cell biological assessment and Project 2 (Proteins to Cell Systems) further explores the prioritized VUS in two dimensional (2-D) and 3-D cell systems. However, due to the complex nature of epilepsy and the brain, uncertainty and even conflicting interpretation will at times arise from in vitro biochemical and cell-based functional assays. Thus, it is ultimately critical to apply refined VUS list for in vivo functional assessment in model organisms. The long-term goal of project 3 (Cell Systems to Preclinical Models) is to incorporate in vivo functional assays into EpiMVP pipeline in which the functional and genetic data of a specific VUS are merged to arrive at a decisive probability of pathogenicity. Project 3 will take advantage of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) gene editing methods to generate well-defined loss-of-function (LOF) epilepsy models in rodent and zebrafish as a null background on which to evaluate human VUS. Data generated in Project 3 will be shared with Projects 1 and 2 and the GVCC in an iterative fashion with an overall deliverable to develop EpiPred (Epilepsy Variant Prediction), a machine learning model that will allow accurate classification of missense epilepsy gene variants as likely pathogenic or benign. With the prioritized and refined VUS list, we will test 3-4 VUS each for 1-2 genes per year and complete testing of at least 5 genes in both fish and rodent model systems. Our first-year goal is to examine functional rescue of 3-4 VUS each for STXBP1 and DEPDC5. Deliverables include: 1) Cross-validated in vivo models to interrogate epilepsy genes; 2) Determination of VUS pathogenicity for at least 5 non-ion channel epilepsy genes using 2 in vivo models; 3) Assessment of in silico and in vitro models for VUS pathogenicity prediction, and whether in vivo models are required for certain genes and VUS; and 4) Optimized in vivo models for each epilepsy gene that will be powerful platforms for future drug discovery and for exploring underlying mechanisms in these genetic epilepsies.