Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions.
Dystonia is characterized by involuntary muscle contractions. Its many forms are genetically, phenotypically and etiologically diverse and it is unknown whether their pathogenesis converges on shared pathways. Mutations in THAP1 [THAP (Thanatos-associated protein) domain containing, apoptosis associ...
| Published in: | PLoS Genetics |
|---|---|
| Main Authors: | Zuchra Zakirova, Tomas Fanutza, Justine Bonet, Ben Readhead, Weijia Zhang, Zhengzi Yi, Genevieve Beauvais, Thomas P Zwaka, Laurie J Ozelius, Robert D Blitzer, Pedro Gonzalez-Alegre, Michelle E Ehrlich |
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2018-01-01
|
| Online Access: | http://europepmc.org/articles/PMC5798844?pdf=render |
Similar Items
THAP1: Role in Mouse Embryonic Stem Cell Survival and Differentiation
by: Francesca Aguilo, et al.
Published: (2017-07-01)
by: Francesca Aguilo, et al.
Published: (2017-07-01)
The DYT6 dystonia causative protein THAP1 is responsible for proteasome activity via PSMB5 transcriptional regulation
by: Yan Wang, et al.
Published: (2025-02-01)
by: Yan Wang, et al.
Published: (2025-02-01)
DYT6 form of idiopathic dystonia
by: M. Yu. Krasnov, et al.
Published: (2017-02-01)
by: M. Yu. Krasnov, et al.
Published: (2017-02-01)
Gait Impairment in Myoclonus–Dystonia (DYT-SGCE)
by: Ghazal Haeri, et al.
Published: (2019-08-01)
by: Ghazal Haeri, et al.
Published: (2019-08-01)
DYT1 dystonia increases risk taking in humans
by: David Arkadir, et al.
Published: (2016-06-01)
by: David Arkadir, et al.
Published: (2016-06-01)
Investigating DYT1 in a Taiwanese dystonia cohort
by: Meng-Chen Wu, et al.
Published: (2022-01-01)
by: Meng-Chen Wu, et al.
Published: (2022-01-01)
Striatal cholinergic interneuron development in models of DYT1 dystonia
by: Lauren N. Miterko-Myers
Published: (2024-05-01)
by: Lauren N. Miterko-Myers
Published: (2024-05-01)
DYT-TOR1A dystonia: an update on pathogenesis and treatment
by: Yuhang Fan, et al.
Published: (2023-08-01)
by: Yuhang Fan, et al.
Published: (2023-08-01)
Evaluation of AZD1446 as a Therapeutic in DYT1 Dystonia
by: Chelsea N. Zimmerman, et al.
Published: (2017-06-01)
by: Chelsea N. Zimmerman, et al.
Published: (2017-06-01)
Generation of a novel rodent model for DYT1 dystonia
by: Kathrin Grundmann, et al.
Published: (2012-07-01)
by: Kathrin Grundmann, et al.
Published: (2012-07-01)
The Effect of Globus Pallidus Interna Deep Brain Stimulation on a Dystonia Patient with the Mutation Compared to Patients with DYT1 and DYT6
by: Jong Hyeon Ahn, et al.
Published: (2019-05-01)
by: Jong Hyeon Ahn, et al.
Published: (2019-05-01)
Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystonia
by: Carlos Henrique F. Camargo, et al.
Published: (2014-10-01)
by: Carlos Henrique F. Camargo, et al.
Published: (2014-10-01)
Neuroimaging findings in DYT1 dystonia and the pathophysiological implication: A systematic review
by: Funmilola T. Taiwo, et al.
Published: (2023-06-01)
by: Funmilola T. Taiwo, et al.
Published: (2023-06-01)
Pre-synaptic release deficits in a DYT1 dystonia mouse model.
by: Fumiaki Yokoi, et al.
Published: (2013-01-01)
by: Fumiaki Yokoi, et al.
Published: (2013-01-01)
Transcriptional regulatory network for neuron-glia interactions and its implication for DYT6 dystonia
by: Dhananjay Yellajoshyula
Published: (2023-10-01)
by: Dhananjay Yellajoshyula
Published: (2023-10-01)
Functional abnormalities in the cerebello-thalamic pathways in a mouse model of DYT25 dystonia
by: Hind Baba Aïssa, et al.
Published: (2022-06-01)
by: Hind Baba Aïssa, et al.
Published: (2022-06-01)
Subtle microstructural changes of the striatum in a DYT1 knock-in mouse model of dystonia
by: Chang-Hyun Song, et al.
Published: (2013-06-01)
by: Chang-Hyun Song, et al.
Published: (2013-06-01)
DYT30 due to VPS16 mutation: An etiology of childhood-onset generalized dystonia
by: Sridhar Shashi, et al.
Published: (2023-01-01)
by: Sridhar Shashi, et al.
Published: (2023-01-01)
TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models
by: Jay Li, et al.
Published: (2020-03-01)
by: Jay Li, et al.
Published: (2020-03-01)
Optogenetic Activation of Striatopallidal Neurons Reveals Altered HCN Gating in DYT1 Dystonia
by: Giuseppe Sciamanna, et al.
Published: (2020-05-01)
by: Giuseppe Sciamanna, et al.
Published: (2020-05-01)
Alteration of striatal dopaminergic neurotransmission in a mouse model of DYT11 myoclonus-dystonia.
by: Lin Zhang, et al.
Published: (2012-01-01)
by: Lin Zhang, et al.
Published: (2012-01-01)
Behavioral signature of trihexyphenidyl in the TOR1A (DYT1) knockin mouse model of dystonia
by: Ahmad Abdal Qader, et al.
Published: (2025-08-01)
by: Ahmad Abdal Qader, et al.
Published: (2025-08-01)
Dystonia type 28 with early onset (DYT-KMT2B): a clinical case
by: V. A. Bulanova, et al.
Published: (2022-12-01)
by: V. A. Bulanova, et al.
Published: (2022-12-01)
Disturbed brain energy metabolism in a rodent model of DYT-TOR1A dystonia
by: Susanne Knorr, et al.
Published: (2024-05-01)
by: Susanne Knorr, et al.
Published: (2024-05-01)
Acute cerebellar knockdown of Sgce reproduces salient features of myoclonus-dystonia (DYT11) in mice
by: Samantha Washburn, et al.
Published: (2019-12-01)
by: Samantha Washburn, et al.
Published: (2019-12-01)
Radiofrequency ablation for DYT‐28 dystonia: short term follow‐up of three adult cases
by: Shiro Horisawa, et al.
Published: (2020-10-01)
by: Shiro Horisawa, et al.
Published: (2020-10-01)
DYT-6 DYSTONIA WITH DRUG INDUCED CHOREA AND AN EXCELLENT RESPONSE TO GPI DEEP BRAIN STIMULATION
by: ZH. MYRZAYEV, et al.
Published: (2022-09-01)
by: ZH. MYRZAYEV, et al.
Published: (2022-09-01)
An Asian Patient with Myoclonus-Dystonia (DYT11) Responsive to Deep Brain Stimulation of the Globus Pallidus Internus
by: Akinori Uruha, et al.
Published: (2014-01-01)
by: Akinori Uruha, et al.
Published: (2014-01-01)
Perturbed Ca2+-dependent signaling of DYT2 hippocalcin mutant as mechanism of autosomal recessive dystonia
by: D.S. Osypenko, et al.
Published: (2019-12-01)
by: D.S. Osypenko, et al.
Published: (2019-12-01)
Dopamine receptor and Gα(olf) expression in DYT1 dystonia mouse models during postnatal development.
by: Lin Zhang, et al.
Published: (2015-01-01)
by: Lin Zhang, et al.
Published: (2015-01-01)
4-Phenylbutyrate attenuates the ER stress response and cyclic AMP accumulation in DYT1 dystonia cell models.
by: Jin A Cho, et al.
Published: (2014-01-01)
by: Jin A Cho, et al.
Published: (2014-01-01)
Mouse model of rare TOR1A variant found in sporadic focal dystonia impairs domains affected in DYT1 dystonia patients and animal models
by: Srishti L. Bhagat, et al.
Published: (2016-09-01)
by: Srishti L. Bhagat, et al.
Published: (2016-09-01)
Case report: Lingual dystonia symptoms treated with botulinum toxin in patients with THAP1 mutation
by: Aparna Wagle Shukla, et al.
Published: (2024-01-01)
by: Aparna Wagle Shukla, et al.
Published: (2024-01-01)
Neural correlates of abnormal sensory discrimination in laryngeal dystonia
by: Pichet Termsarasab, et al.
Published: (2016-01-01)
by: Pichet Termsarasab, et al.
Published: (2016-01-01)
In vivo imaging reveals impaired connectivity across cortical and subcortical networks in a mouse model of DYT1 dystonia
by: Jesse C. DeSimone, et al.
Published: (2016-11-01)
by: Jesse C. DeSimone, et al.
Published: (2016-11-01)
RGS9‐2 rescues dopamine D2 receptor levels and signaling in DYT1 dystonia mouse models
by: Paola Bonsi, et al.
Published: (2018-12-01)
by: Paola Bonsi, et al.
Published: (2018-12-01)
The nuclear envelope localization of DYT1 dystonia torsinA-ΔE requires the SUN1 LINC complex component
by: Jeong Danielle Y, et al.
Published: (2011-05-01)
by: Jeong Danielle Y, et al.
Published: (2011-05-01)
DYT1 knock-in mice are not sensitized against mitochondrial complex-II inhibition.
by: Nicole Bode, et al.
Published: (2012-01-01)
by: Nicole Bode, et al.
Published: (2012-01-01)
Loss-of-function mutations in the dystonia gene THAP1 impair proteasome function by inhibiting PSMB5 expression
by: Dylan E. Ramage, et al.
Published: (2025-02-01)
by: Dylan E. Ramage, et al.
Published: (2025-02-01)
The zebrafish homologue of the human DYT1 dystonia gene is widely expressed in CNS neurons but non-essential for early motor system development.
by: Jonathan J Sager, et al.
Published: (2012-01-01)
by: Jonathan J Sager, et al.
Published: (2012-01-01)
Similar Items
-
THAP1: Role in Mouse Embryonic Stem Cell Survival and Differentiation
by: Francesca Aguilo, et al.
Published: (2017-07-01) -
The DYT6 dystonia causative protein THAP1 is responsible for proteasome activity via PSMB5 transcriptional regulation
by: Yan Wang, et al.
Published: (2025-02-01) -
DYT6 form of idiopathic dystonia
by: M. Yu. Krasnov, et al.
Published: (2017-02-01) -
Gait Impairment in Myoclonus–Dystonia (DYT-SGCE)
by: Ghazal Haeri, et al.
Published: (2019-08-01) -
DYT1 dystonia increases risk taking in humans
by: David Arkadir, et al.
Published: (2016-06-01)
