Evidence for the involvement of Puralpha in response to DNA replication stress.

Huichen Wang, Meijuan Wang, Krzysztof Reiss, Nune Darbinian-Sarkissian, Edward M Johnson, George Iliakis, Shohreh Amini, Kamel Khalili, Jay Rappaport

Department of Neuroscience, Center for Neurovirology, Temple University School of Medicine, Philadelphia, Pennsylvania 19122, USA.

Journal Article: Cancer biology & therapy (impact factor: 2.71). 05/2007; 6(4):596-602.

Abstract

Puralpha is a sequence-specific nucleic acid binding protein that is involved in multiple cellular functions including regulation of transcription, initiation of DNA replication, cell cycle progression, and neuronal cell differentiation. Its potential role in DNA repair has not been explored. We have now analyzed the role of Puralpha in the cellular response to replication-associated DNA repair of double-strand breaks (DSBs) using Puralpha knockout mouse embryo fibroblasts (MEFs). We found that Puralpha negative cells are hypersensitive to the DNA replication inhibitor, hydroxyurea (HU), and that HU induces excessive DSBs, which delayed the resumption of cell cycle progression after HU treatment. Reintroduction of Pura into Pura null cells reduced the accumulation of DSBs and enhanced DNA end joining. These results suggest a role for Puralpha as a caretaker protein that is involved in the repair of DSBs induced by stalled replication forks.

Source: PubMed

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Keywords

cell cycle progression
 
cellular response
 
DNA end
 
DNA replication
 
DNA replication inhibitor
 
double-strand breaks
 
DSBs
 
DSBs induced
 
HU induces excessive DSBs
 
multiple cellular functions
 
neuronal cell differentiation
 
potential role
 
Pura null cells
 
Puralpha
 
Puralpha knockout mouse embryo fibroblasts
 
Puralpha negative cells
 
Reintroduction
 
replication forks
 
replication-associated DNA
 
sequence-specific nucleic acid binding protein