Endonuclease G: A role for the enzyme in recombination and cellular proliferation
Recombination, Genetic
0301 basic medicine
Endodeoxyribonucleases
Base Sequence
Cell Survival
Cell Cycle
Molecular Sequence Data
Herpesvirus 1, Human
3. Good health
03 medical and health sciences
Chlorocebus aethiops
Animals
Humans
RNA Interference
Vero Cells
Cell Proliferation
DOI:
10.1073/pnas.0603445103
Publication Date:
2006-06-06T00:58:40Z
AUTHORS (3)
ABSTRACT
Our earlier studies had suggested that endonuclease G (EndoG), a member of the evolutionarily conserved DNA/RNA nonspecific ββα-Me-finger nuclease family, functioned in the
a
sequence-mediated segment inversion observed during herpes simplex virus 1 replication. To test this hypothesis, we used RNA interference to reduce the level of EndoG in mammalian cells in culture. Reduction of EndoG produced a small but statistically significant decrease in
a
sequence-mediated recombination, suggesting that EndoG does play a role in this process. We also observed that reduction in the level of EndoG resulted in a deficiency in cell proliferation. Cells with a reduced level of EndoG also showed changes in cell distribution in the cell cycle, producing a pattern characteristic of cells that have been arrested in the G
2
phase. These findings suggest that EndoG is required for normal cellular proliferation.
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