| Literature DB >> 26948891 |
Jennifer L Hazen1, Gregory G Faust2, Alberto R Rodriguez3, William C Ferguson1, Svetlana Shumilina2, Royden A Clark2, Michael J Boland1, Greg Martin3, Pavel Chubukov1,4, Rachel K Tsunemoto1,5, Ali Torkamani4, Sergey Kupriyanov3, Ira M Hall6,7, Kristin K Baldwin1,5.
Abstract
Somatic mutation in neurons is linked to neurologic disease and implicated in cell-type diversification. However, the origin, extent, and patterns of genomic mutation in neurons remain unknown. We established a nuclear transfer method to clonally amplify the genomes of neurons from adult mice for whole-genome sequencing. Comprehensive mutation detection and independent validation revealed that individual neurons harbor ∼100 unique mutations from all classes but lack recurrent rearrangements. Most neurons contain at least one gene-disrupting mutation and rare (0-2) mobile element insertions. The frequency and gene bias of neuronal mutations differ from other lineages, potentially due to novel mechanisms governing postmitotic mutation. Fertile mice were cloned from several neurons, establishing the compatibility of mutated adult neuronal genomes with reprogramming to pluripotency and development.Entities:
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Year: 2016 PMID: 26948891 PMCID: PMC4795965 DOI: 10.1016/j.neuron.2016.02.004
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173