Document Detail


The molecular links between TDP-43 dysfunction and neurodegeneration.
MedLine Citation:
PMID:  19737636     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
TDP-43 nuclear protein is involved in several major neurodegenerative diseases that include frontotemporal lobar degeneration with ubiquitin (FTLD-U) bodies and amyotrophic lateral sclerosis (ALS). As a consequence, the role played by this protein in both normal and diseased cellular metabolism has come under very close scrutiny. In the neuronal tissues of affected individuals TDP-43 undergoes aberrant localization to the cytoplasm to form insoluble aggregates. Furthermore, it is subject to degradation, ubiquitination, and phosphorylation. Understanding the pathways that lead to these changes will be crucial to define the functional role played by this protein in disease. Several recent biochemical and molecular studies have provided new information regarding the potential physiological consequences of these modifications. Moreover, the discovery of TDP-43 mutations associated with disease in a limited number of cases and the data from existing animal models have strengthened the proposed links between this protein and disease. In this review we will discuss the available data regarding the biochemical and functional changes that transform the wild-type endogenous TDP-43 in its pathological form. Furthermore, we will concentrate on examining the potential pathological mechanisms mediated by TDP-43 in different gain- versus loss-of-function scenarios. In the near future, this knowledge will hopefully increase our knowledge on disease progression and development. Moreover, it will allow the design of innovative therapeutic strategies for these pathologies based on the specific molecular defects causing the disease.
Authors:
Emanuele Buratti; Francisco E Baralle
Related Documents :
20225336 - Autophagy: cellular and molecular mechanisms.
19766516 - Cerebral folate deficiency and cns inflammatory markers in alpers disease.
17273806 - Hallmarks of protein oxidative damage in neurodegenerative diseases: focus on alzheimer...
15878696 - Role of mitochondrial dna in toxic responses to oxidative stress.
2058526 - A new algorithm for the diagnosis of polycythemia.
15692786 - Defense mechanisms in inflammatory bowel disease.
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review    
Journal Detail:
Title:  Advances in genetics     Volume:  66     ISSN:  0065-2660     ISO Abbreviation:  Adv. Genet.     Publication Date:  2009  
Date Detail:
Created Date:  2009-09-09     Completed Date:  2009-10-06     Revised Date:  2011-11-24    
Medline Journal Info:
Nlm Unique ID:  0370421     Medline TA:  Adv Genet     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1-34     Citation Subset:  IM    
Affiliation:
International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Amyotrophic Lateral Sclerosis / genetics,  metabolism,  pathology
Animals
DNA-Binding Proteins / genetics*,  metabolism*
Humans
Nerve Degeneration / metabolism*,  pathology
Grant Support
ID/Acronym/Agency:
GGP06147//Telethon
Chemical
Reg. No./Substance:
0/DNA-Binding Proteins; 0/protein TDP-43

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Obstructive apneas and severe dysphagia in a girl with Townes-Brocks syndrome and atypical feet invo...
Next Document:  Resources and strategies to integrate the study of ethical, legal, and social implications of geneti...