Open AccessPharmacological perturbation reveals deficits in D2 receptor responses in Thap1 null mice
Author(s) -
Frederick Natalie M.,
Pooler Morgan M.,
Shah Parth,
Didonna Alessandro,
Opal Puneet
Publication year - 2021
Publication title -
annals of clinical and translational neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.824
H-Index - 42
ISSN - 2328-9503
DOI - 10.1002/acn3.51481
Subject(s) - dopaminergic , receptor , transcription factor , gene , biology , medicine , genetics , pharmacology , neuroscience , dopamine
Abstract The primary dystonia DYT6 is caused by mutations in the transcription factor Thanatos‐associated protein 1 (THAP1). To understand THAP1’s functions, we generated mice lacking THAP1 in the nervous system. THAP1 loss causes locomotor deficits associated with transcriptional changes. Since many of the genes misregulated involve dopaminergic signaling, we pharmacologically challenged the two striatal canonical dopamine pathways: the direct, regulated by the D1 receptor, and the indirect, regulated by the D2 receptor. We discovered that depleting THAP1 specifically interferes with the D2 receptor responses, pointing to a selective misregulation of the indirect pathway in DYT6 with implications for pathogenesis and treatment.