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TDP-43 Functions and Pathogenic Mechanisms Implicated in TDP-43 Proteinopathies

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Journal Trends Mol Med
Date 2011 Jul 26
PMID 21783422
Citations 136
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Abstract

Given the critical role for TDP-43 in diverse neurodegenerative diseases including amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD-TDP), there has been a recent surge in efforts to understand the normal functions of TDP-43 and the molecular basis of dysregulation that occurs in TDP-43 proteinopathies. Here, we highlight recent findings examining TDP-43 molecular functions with particular emphasis on stress-mediated regulation of TDP-43 localization, putative downstream TDP-43 target genes and RNAs, as well as TDP-43 interacting proteins, all of which represent viable points of therapeutic intervention for ALS, FTLD-TDP and related proteinopathies. Finally, we review current mouse models of TDP-43 and discuss their similarities and potential relevance to human TDP-43 proteinopathies including ALS and FTLD-TDP.

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References
1.
Ule J . Ribonucleoprotein complexes in neurologic diseases. Curr Opin Neurobiol. 2008; 18(5):516-23. DOI: 10.1016/j.conb.2008.09.018. View

2.
Polymenidou M, Lagier-Tourenne C, Hutt K, Huelga S, Moran J, Liang T . Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. Nat Neurosci. 2011; 14(4):459-68. PMC: 3094729. DOI: 10.1038/nn.2779. View

3.
Buratti E, Dork T, Zuccato E, Pagani F, Romano M, Baralle F . Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping. EMBO J. 2001; 20(7):1774-84. PMC: 145463. DOI: 10.1093/emboj/20.7.1774. View

4.
Elden A, Kim H, Hart M, Chen-Plotkin A, Johnson B, Fang X . Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS. Nature. 2010; 466(7310):1069-75. PMC: 2965417. DOI: 10.1038/nature09320. View

5.
Damiano M, Galvan L, Deglon N, Brouillet E . Mitochondria in Huntington's disease. Biochim Biophys Acta. 2009; 1802(1):52-61. DOI: 10.1016/j.bbadis.2009.07.012. View