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ABSTRACT: Background
The ribonuclear protein TDP-43 has been implicated in the pathophysiology of amyotrophic lateral sclerosis (ALS), with genetic mutations being linked to the neurological symptoms of the disease. Though alterations in the intracellular distribution of TDP-43 have been observed in skeletal muscles of patients suffering from ALS, it is not clear whether such modifications play an active role in the disease or merely represent an expression of muscle homeostatic mechanisms. Also, the molecular and metabolic pathways regulated by TDP-43 in the skeletal muscle remain largely unknown. Here, we analyze the function of TBPH, the Drosophila melanogaster ortholog of TDP-43, in skeletal muscles.Results
We modulated the activity of TDP-43 in Drosophila muscles by means of RNA
SUBMITTER: Strah N
PROVIDER: S-EPMC7099817 | biostudies-literature | 2020 Mar
REPOSITORIES: biostudies-literature