http://www.cnr.it/ontology/cnr/individuo/prodotto/ID13659
DNA polymerase-beta is expressed early in neurons of Alzheimer's disease brain and is loaded into DNA replication forks in neurons challenged with beta-amyloid. (Articolo in rivista)
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- Label
- DNA polymerase-beta is expressed early in neurons of Alzheimer's disease brain and is loaded into DNA replication forks in neurons challenged with beta-amyloid. (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1523/JNEUROSCI.2793-06.2006 (literal)
- Alternative label
A. Copani, JJ. Hoozemans, F. Caraci, M. Calafiore, E.S. Van Haastert, R. Veerhuis, A.J. Rozemuller, E. Aronica, M.A. Sortino, F. Nicoletti. (2006)
DNA polymerase-beta is expressed early in neurons of Alzheimer's disease brain and is loaded into DNA replication forks in neurons challenged with beta-amyloid.
in The journal of neuroscience (Online)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- A. Copani, JJ. Hoozemans, F. Caraci, M. Calafiore, E.S. Van Haastert, R. Veerhuis, A.J. Rozemuller, E. Aronica, M.A. Sortino, F. Nicoletti. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
- I.F. 7.453
Times Cited: 29 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Department of Pharmaceutical Sciences, University of Catania, 95125 Catania, Italy. (literal)
- Titolo
- DNA polymerase-beta is expressed early in neurons of Alzheimer's disease brain and is loaded into DNA replication forks in neurons challenged with beta-amyloid. (literal)
- Abstract
- J Neurosci. 2006 Oct 25;26(43):10949-57.
DNA polymerase-beta is expressed early in neurons of Alzheimer's disease brain
and is loaded into DNA replication forks in neurons challenged with beta-amyloid.
Copani A, Hoozemans JJ, Caraci F, Calafiore M, Van Haastert ES, Veerhuis R,
Rozemuller AJ, Aronica E, Sortino MA, Nicoletti F.
Department of Pharmaceutical Sciences, University of Catania, 95125 Catania,
Italy. acopani@katamail.com
Cultured neurons exposed to synthetic beta-amyloid (Abeta) fragments reenter the
cell cycle and initiate a pathway of DNA replication that involves the repair
enzyme DNA polymerase-beta (DNA pol-beta) before undergoing apoptotic death. In
this study, by performing coimmunoprecipitation experiments on cross-linked
nucleoprotein fragments from Abeta-treated neurons, we demonstrate that DNA
pol-beta coimmunoprecipitates with cell division cycle 45 (Cdc45) and with DNA
primase in short nucleoprotein fragments. This indicates that DNA pol-beta is
loaded into neuronal DNA replication forks after Abeta treatment. In response to
Abeta the canonical DNA-synthesizing enzyme DNA pol-delta also was loaded into
neuronal replication forks, but at later times than DNA pol-beta. Methoxyamine,
an inhibitor of the apurinic/apyrimidinic endonuclease that allows for the
recruitment of DNA pol-beta during the process of base excision repair (BER),
failed to affect coimmunoprecipitation between DNA pol-beta and Cdc45, indicating
that DNA pol-beta loading to the replication forks is independent of DNA breaks.
However, methoxyamine reduced DNA replication and ensuing apoptosis in neurons
exposed to Abeta, suggesting that an efficient BER process allows DNA replication
to proceed up to the threshold for death. These data demonstrate that DNA
pol-beta is an essential component of the DNA replication machinery in
Abeta-treated neurons and additionally support the hypothesis of a close
association of cell cycle events with neuronal death in Alzheimer's disease (AD).
Accordingly, by investigating the neuronal expression of DNA pol-beta, along with
phosphorylated retinoblastoma protein and neurofibrillary changes in AD brain, we
show an early involvement of DNA pol-beta in the pathogenesis of AD. (literal)
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