Deciphering the genomics of gene network regulation of T cell and fibroblast states in autoimmune inflammation

About This Grant

NO CHANGE FROM ORIGINAL SUBMISSION Abstract Natural genetic variation impacts most human diseases, yet predicting how regulatory variants control gene expression and ultimately disease phenotypes poses considerable challenges. First, the polygenic inheritance influencing most conditions requires consideration of a vast number of genes and regulatory elements. This task is challenged by the complexity of gene regulation, where 3D regulatory interactions can link enhancers and genes over large genomic distances. Second, multiple interacting cell types are often dysregulated in disease pathology. This necessitates an understanding of how the collective variants associating with a disease affect each cell type involved in the disease process and subsequently how these dysregulated cellular phenotypes crossregulate and drive subsequent cellular states. In this IGVF project, we will use rheumatoid arthritis (RA), a human autoimmune inflammatory disease, as a case study to develop robust machine learning models of gene regulation to decipher the impact of genomic variation on multiple cellular drivers of pathology—namely, inflammatory T cell and fibroblast subsets found in affected joint tissue. The choice of RA is motivated by its public health importance, specified target tissue, access to clinical samples, considerable knowledge of disease-associated gene loci, and our team’s complementary expertise in machine learning, RA pathophysiology, immunology and inflammation, and single-cell functional genomics. We will develop an advanced machine learning framework to model the effects of allelic variation on gene regulatory networks based on the analysis of epigenomes, transcriptomes, and connectomes of mouse activated T cells and synovial fibroblasts and extend these models to RA patient joint tissue and primary cells. We will train allele-specific gene regulatory models (GRMs) that account for long-range regulatory interactions by integrating single-cell transcriptome and epigenome (sc-multiome) data with bulk 3D interactome analyses. A notable feature of our approach is that we leverage the genetic diversity of evolutionarily distant F1 hybrid mice to provide robust training data for these models, and then apply these advances to the human context through transfer learning. Highly parallelized Perturb-seq experiments in primary synovial fibroblasts from RA patients with single-cell multiomic readouts will then be used to evaluate and refine regulatory models and to train network models that connect gene expression programs to phenotype. Finally, we will combine spatial and single-cell transcriptomics conducted on samples from RA inflamed joints to model the organization and interactions between T cells and sedentary tissue-organizing fibroblasts within local cellular communities. The predictive GRMs that will be generated from our study along with the experimental systems for human disease will be readily transferrable to other polygenic disorders which must consider complex regulatory genomic networks for various interacting cell types in affected tissues.