Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disorder. In motor neurons of ALS, TAR DNA binding protein-43 (TDP-43), a nuclear protein encoded by TARDBP, is absent from the nucleus and forms cytoplasmic inclusions. TDP-43 auto-regulates the amount by regulating the TARDBP mRNA, which...
Main Authors: | Koyama, Akihide, Sugai, Akihiro, Kato, Taisuke, Ishihara, Tomohiko, Shiga, Atsushi, Toyoshima, Yasuko, Koyama, Misaki, Konno, Takuya, Hirokawa, Sachiko, Yokoseki, Akio, Nishizawa, Masatoyo, Kakita, Akiyoshi, Takahashi, Hitoshi, Onodera, Osamu |
---|---|
Format: | Online |
Language: | English |
Published: |
Oxford University Press
2016
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4937342/ |
Similar Items
-
Alteration of POLDIP3 Splicing Associated with Loss of Function of TDP-43 in Tissues Affected with ALS
by: Shiga, Atsushi, et al.
Published: (2012) -
Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes
by: Takeuchi, Ryoko, et al.
Published: (2016) -
Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends
by: Takahashi, Tetsuya, et al.
Published: (2007) -
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia
by: Quadri, Marialuisa, et al.
Published: (2011) -
Endogenous progesterone levels and frontotemporal dementia: modulation of TDP-43 and Tau levels in vitro and treatment of the A315T TARDBP mouse model
by: Dang, Theresa N. T., et al.
Published: (2013)