Transcriptomics

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Pathways Disrupted in Human ALS Motor Neurons Identified Through Genetic Correction of Mutant SOD1


ABSTRACT: Although many distinct mutations in a variety of genes are known to cause Amyotrophic Lateral Sclerosis (ALS), it remains poorly understood how they selectively impact motor neuron biology and whether they converge on common pathways to cause neural degeneration. Here, we have combined reprogramming and stem cell differentiation approaches with genome engineering and RNA sequencing to define the transcriptional changes that are induced in human motor neurons by mutant SOD1. Mutant SOD1 protein induced a transcriptional signature indicative of increased oxidative stress, reduced mitochondrial function, altered sub-cellular transport as well as activation of the ER stress and unfolded protein response pathways. Functional studies demonstrated that perturbations in these pathways were indeed the source of altered transcript levels.

ORGANISM(S): Homo sapiens

PROVIDER: GSE54409 | GEO | 2014/02/03

SECONDARY ACCESSION(S): PRJNA236453

REPOSITORIES: GEO

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