Genetic loss and gain of function in mice have typically been studied by using knockout or knockin mice that take months to years to generate. To address this problem for the nervous system, we developed NEPTUNE (NEural Plate Targeting by NanoinjEction) to rapidly and flexibly transduce the neural plate with virus prior to neurulation, and thus manipulate the future nervous system. Stable integration in >95% of cells in the brain enabled long-term overexpression, and conditional expression was achieved by using cell-type-specific MiniPromoters. Knockdown of by using NEPTUNE recapitulated the phenotype of embryos. We used NEPTUNE to investigate , mutations in which cause spinocerebellar ataxia type 5. knockdown induced dose-dependent defects in the neural tube, embryonic turning, and abdominal wall closure, previously unreported functions for . NEPTUNE thus offers a rapid and cost-effective technique to test gene function in the nervous system and can reveal phenotypes incompatible with life.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457050 | PMC |
http://dx.doi.org/10.1016/j.crmeth.2021.100043 | DOI Listing |
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