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PMID: 12539243 Published · ppublish English Journal Article Review

When parsimony backfires: neglecting DNA repair may doom neurons in Alzheimer's disease.

Nouspikel T, Hanawalt PC

Abstract

Taking advantage of the fact that they need not replicate their DNA, terminally differentiated neurons only repair their expressed genes and largely dispense with the burden of removing damage from most of their genome. However, they may pay a heavy price for this laxity if unforeseen circumstances, such as a pathological condition like Alzheimer's disease, cause them to re-enter the cell cycle. The lifetime accumulation of unrepaired lesions in the silent genes of neurons is likely to be significant and may result in aborting the mitotic process and triggering cell death if the cells attempt to express these dormant genes and resume DNA replication.

MeSH Terms
Alzheimer Disease/etiology,metabolism,pathology Cell Cycle Cell Death DNA Damage DNA Repair Gene Expression Humans Models, Neurological Neurons/metabolism,pathology
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Nouspikel Thierry
Department of Biological Sciences, Stanford University, CA 94305-5020, USA. [email protected]
Hanawalt Philip C
Article Info
Journal
BioEssays : news and reviews in molecular, cellular and developmental biology
Abbr.
Bioessays
ISSN
0265-9247
Published
2003-02-00
Pages
168-73
Language
English
Region
United States
NLM ID
8510851
Subset
IM
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