Genetic and epigenetic editing in
nervous system
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Dialogues Clin Neurosci

Author affiliations: Department of Neurobiology, University of Alabama at Birmingham, Alabama, US. Address for correspondence: Jeremy J. Day, PhD, Associate Professor, Department of Neurobiology, University of Alabama at Birmingham, 910 Shelby Building, 1825 University Blvd, Birmingham, AL 35294, US. 
(email:

Published: December 2019

Numerous neuronal functions depend on the precise spatiotemporal regulation of gene expression, and the cellular machinery that contributes to this regulation is frequently disrupted in neurodevelopmental, neuropsychiatric, and neurological disease states. Recent advances in gene editing technology have enabled increasingly rapid understanding of gene sequence variation and gene regulatory function in the central nervous system. Moreover, these tools have provided new insights into the locus-specific functions of epigenetic modifications and enabled epigenetic editing at specific gene loci in disease contexts. Continued development of clustered regularly interspaced short palindromic repeats (CRISPR)-based tools has provided not only cell-specific modulation, but also rapid induction profiles that permit sophisticated interrogation of the temporal dynamics that contribute to brain health and disease. This review summarizes recent advances in genetic editing, transcriptional modulation, and epigenetic reorganization, with a focus on applications to neuronal systems and potential uses in brain disorders characterized by genetic sequence variation or transcriptional dysregulation.
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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952749PMC
http://dx.doi.org/10.31887/DCNS.2019.21.4/jdayDOI Listing

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