TY - JOUR
T1 - Polyphosphate is a key factor for cell survival after DNA damage in eukaryotic cells
AU - Bru, Samuel
AU - Samper-Martín, Bàrbara
AU - Quandt, Eva
AU - Hernández-Ortega, Sara
AU - Martínez-Laínez, Joan M.
AU - Garí, Eloi
AU - Rafel, Marta
AU - Torres-Torronteras, Javier
AU - Martí, Ramón
AU - Ribeiro, Mariana P.C.
AU - Jiménez, Javier
AU - Clotet, Josep
PY - 2017/9/1
Y1 - 2017/9/1
N2 - © 2017 Elsevier B.V. Cells require extra amounts of dNTPs to repair DNA after damage. Polyphosphate (polyP) is an evolutionary conserved linear polymer of up to several hundred inorganic phosphate (Pi) residues that is involved in many functions, including Pi storage. In the present article, we report on findings demonstrating that polyP functions as a source of Pi when required to sustain the dNTP increment essential for DNA repair after damage. We show that mutant yeast cells without polyP produce less dNTPs upon DNA damage and that their survival is compromised. In contrast, when polyP levels are ectopically increased, yeast cells become more resistant to DNA damage. More importantly, we show that when polyP is reduced in HEK293 mammalian cell line cells and in human dermal primary fibroblasts (HDFa), these cells become more sensitive to DNA damage, suggesting that the protective role of polyP against DNA damage is evolutionary conserved. In conclusion, we present polyP as a molecule involved in resistance to DNA damage and suggest that polyP may be a putative target for new approaches in cancer treatment or prevention.
AB - © 2017 Elsevier B.V. Cells require extra amounts of dNTPs to repair DNA after damage. Polyphosphate (polyP) is an evolutionary conserved linear polymer of up to several hundred inorganic phosphate (Pi) residues that is involved in many functions, including Pi storage. In the present article, we report on findings demonstrating that polyP functions as a source of Pi when required to sustain the dNTP increment essential for DNA repair after damage. We show that mutant yeast cells without polyP produce less dNTPs upon DNA damage and that their survival is compromised. In contrast, when polyP levels are ectopically increased, yeast cells become more resistant to DNA damage. More importantly, we show that when polyP is reduced in HEK293 mammalian cell line cells and in human dermal primary fibroblasts (HDFa), these cells become more sensitive to DNA damage, suggesting that the protective role of polyP against DNA damage is evolutionary conserved. In conclusion, we present polyP as a molecule involved in resistance to DNA damage and suggest that polyP may be a putative target for new approaches in cancer treatment or prevention.
KW - DNA damage
KW - Human dermal fibroblasts
KW - Mammalian cells
KW - Polyphosphate
KW - Repair
KW - Saccharomyces
U2 - 10.1016/j.dnarep.2017.08.001
DO - 10.1016/j.dnarep.2017.08.001
M3 - Article
SN - 1568-7864
VL - 57
SP - 171
EP - 178
JO - DNA Repair
JF - DNA Repair
ER -