Literature DB >> 19285963

Identification of casein kinase-1 phosphorylation sites on TDP-43.

Fuyuki Kametani1, Takashi Nonaka, Takehiro Suzuki, Tetsuaki Arai, Naoshi Dohmae, Haruhiko Akiyama, Masato Hasegawa.   

Abstract

TAR DNA-binding protein of 43 kDa (TDP-43) is deposited as hyperphosphorylated cytoplasmic and intranuclear inclusions in brains of patients with frontotemporal lobar degeneration with ubiquitinated inclusions and amyotrophic lateral sclerosis. In this study, we identified 29 phosphorylation sites on recombinant TDP-43 that are phosphorylated by casein kinase-1 (CK1). Interestingly, 18 of them were located in the C-terminal glycine-rich region of TDP-43. Our results indicate that CK1-mediated phosphorylation may play a role in the pathogenesis of these diseases.

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Year:  2009        PMID: 19285963     DOI: 10.1016/j.bbrc.2009.03.038

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  43 in total

Review 1.  Review: transactive response DNA-binding protein 43 (TDP-43): mechanisms of neurodegeneration.

Authors:  T F Gendron; K A Josephs; L Petrucelli
Journal:  Neuropathol Appl Neurobiol       Date:  2010-02-19       Impact factor: 8.090

2.  Dysregulation of TDP-43 intracellular localization and early onset ALS are associated with a TARDBP S375G variant.

Authors:  Kathy Newell; Francesca Paron; Miguel Mompean; Jill Murrell; Elisa Salis; Cristiana Stuani; Gary Pattee; Maurizio Romano; Douglas Laurents; Bernardino Ghetti; Emanuele Buratti
Journal:  Brain Pathol       Date:  2018-12-27       Impact factor: 6.508

Review 3.  Friend or foe-Post-translational modifications as regulators of phase separation and RNP granule dynamics.

Authors:  Mario Hofweber; Dorothee Dormann
Journal:  J Biol Chem       Date:  2018-12-26       Impact factor: 5.157

4.  Transactive response DNA-binding protein 43 (TDP-43) regulates alternative splicing of tau exon 10: Implications for the pathogenesis of tauopathies.

Authors:  Jianlan Gu; Feng Chen; Khalid Iqbal; Cheng-Xin Gong; Xinglong Wang; Fei Liu
Journal:  J Biol Chem       Date:  2017-05-09       Impact factor: 5.157

5.  An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity.

Authors:  Weirui Guo; Yanbo Chen; Xiaohong Zhou; Amar Kar; Payal Ray; Xiaoping Chen; Elizabeth J Rao; Mengxue Yang; Haihong Ye; Li Zhu; Jianghong Liu; Meng Xu; Yanlian Yang; Chen Wang; David Zhang; Eileen H Bigio; Marsel Mesulam; Yan Shen; Qi Xu; Kazuo Fushimi; Jane Y Wu
Journal:  Nat Struct Mol Biol       Date:  2011-06-12       Impact factor: 15.369

6.  An acetylation switch controls TDP-43 function and aggregation propensity.

Authors:  Todd J Cohen; Andrew W Hwang; Clark R Restrepo; Chao-Xing Yuan; John Q Trojanowski; Virginia M Y Lee
Journal:  Nat Commun       Date:  2015-01-05       Impact factor: 14.919

Review 7.  Structure, regulation, and (patho-)physiological functions of the stress-induced protein kinase CK1 delta (CSNK1D).

Authors:  Pengfei Xu; Chiara Ianes; Fabian Gärtner; Congxing Liu; Timo Burster; Vasiliy Bakulev; Najma Rachidi; Uwe Knippschild; Joachim Bischof
Journal:  Gene       Date:  2019-07-31       Impact factor: 3.688

8.  CDC7 inhibition blocks pathological TDP-43 phosphorylation and neurodegeneration.

Authors:  Nicole F Liachko; Pamela J McMillan; Chris R Guthrie; Thomas D Bird; James B Leverenz; Brian C Kraemer
Journal:  Ann Neurol       Date:  2013-07-08       Impact factor: 10.422

9.  Mitochondrial dysfunction and decrease in body weight of a transgenic knock-in mouse model for TDP-43.

Authors:  Carola Stribl; Aladin Samara; Dietrich Trümbach; Regina Peis; Manuela Neumann; Helmut Fuchs; Valerie Gailus-Durner; Martin Hrabě de Angelis; Birgit Rathkolb; Eckhard Wolf; Johannes Beckers; Marion Horsch; Frauke Neff; Elisabeth Kremmer; Sebastian Koob; Andreas S Reichert; Wolfgang Hans; Jan Rozman; Martin Klingenspor; Michaela Aichler; Axel Karl Walch; Lore Becker; Thomas Klopstock; Lisa Glasl; Sabine M Hölter; Wolfgang Wurst; Thomas Floss
Journal:  J Biol Chem       Date:  2014-02-10       Impact factor: 5.157

10.  ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain.

Authors:  Alexander E Conicella; Gül H Zerze; Jeetain Mittal; Nicolas L Fawzi
Journal:  Structure       Date:  2016-08-18       Impact factor: 5.006

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