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Neuron DOI:10.1016/j.neuron.2020.01.004

Genome-wide In Vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT Toxicity.

Publication TypeJournal Article
Year of Publication2020
AuthorsWertz, MH, Mitchem, MR, S Pineda, S, Hachigian, LJ, Lee, H, Lau, V, Powers, A, Kulicke, R, Madan, GK, Colic, M, Therrien, M, Vernon, A, Beja-Glasser, VF, Hegde, M, Gao, F, Kellis, M, Hart, T, Doench, JG, Heiman, M
JournalNeuron
Date Published2020 Jan 24
ISSN1097-4199
Abstract

Unbiased in vivo genome-wide genetic screening is a powerful approach to elucidate new molecular mechanisms, but such screening has not been possible to perform in the mammalian central nervous system (CNS). Here, we report the results of the first genome-wide genetic screens in the CNS using both short hairpin RNA (shRNA) and CRISPR libraries. Our screens identify many classes of CNS neuronal essential genes and demonstrate that CNS neurons are particularly sensitive not only to perturbations to synaptic processes but also autophagy, proteostasis, mRNA processing, and mitochondrial function. These results reveal a molecular logic for the common implication of these pathways across multiple neurodegenerative diseases. To further identify disease-relevant genetic modifiers, we applied our screening approach to two mouse models of Huntington's disease (HD). Top mutant huntingtin toxicity modifier genes included several Nme genes and several genes involved in methylation-dependent chromatin silencing and dopamine signaling, results that reveal new HD therapeutic target pathways.

DOI10.1016/j.neuron.2020.01.004
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/32004439?dopt=Abstract

Alternate JournalNeuron
PubMed ID32004439