Cell type-specific enhancer-promoter connectivity maps in the human brain and disease risk association
Nott, A.; Holtman, I. R.; Coufal, N. G.; Schlachetzki, J. C. M.; Yu, M.; Hu, R.; Han, C. Z.; Pena, M.; Xiao, J.; Wu, Y.; Keuelen, Z.; Pasillas, M. P.; O'Connor, C.; Schafer, S. T.; Shen, Z.; Rissman, R. A.; Brewer, J. B.; Gosselin, D.; Gonda, D. D.; Levy, M. L.; Rosenfeld, M. G.; McVicker, G. P.; Gage, F. H.; Ren, B.; Glass, C. K.
Show abstract
Unique cell type-specific patterns of activated enhancers can be leveraged to interpret non-coding genetic variation associated with complex traits and diseases such as neurological and psychiatric disorders. Here, we have defined active promoters and enhancers for major cell types of the human brain. Whereas psychiatric disorders were primarily associated with regulatory regions in neurons, idiopathic Alzheimers disease (AD) variants were largely confined to microglia enhancers. Interactome maps connecting GWAS variants in cell type-specific enhancers to gene promoters revealed an extended microglia gene network in AD. Deletion of a microglia-specific enhancer harboring AD-risk variants ablated BIN1 expression in microglia but not in neurons or astrocytes. These findings revise and expand the genes likely to be influenced by non-coding variants in AD and suggest the probable brain cell types in which they function.\n\nOne Sentence SummaryIdentification of cell type-specific regulatory elements in the human brain enables interpretation of non-coding GWAS risk variants.
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