RRC ID 71932
Author Yamashita S, Tanaka M, Ida C, Kouyama K, Nakae S, Matsuki T, Tsuda M, Shirai T, Kamemura K, Nishi Y, Moss J, Miwa M.
Title Physiological levels of poly(ADP-ribose) during the cell cycle regulate HeLa cell proliferation.
Journal Exp Cell Res
Abstract Protein targets of polyADP-ribosylation undergo covalent modification with high-molecular-weight, branched poly(ADP-ribose) (PAR) of lengths up to 200 or more ADP-ribose residues derived from NAD+. PAR polymerase 1 (PARP1) is the most abundant and well-characterized enzyme involved in PAR biosynthesis. Extensive studies have been carried out to determine how polyADP-ribosylation (PARylation) regulates cell proliferation during cell cycle, with conflicting conclusions. Since significant activation of PARP1 occurs during cell lysis in vitro, we changed the standard method for cell lysis, and using our sensitive ELISA system, quantified without addition of a PAR glycohydrolase inhibitor and clarified that the PAR level is significantly higher in S phase than that in G1. Under normal condition in the absence of exogenous DNA-damaging agent, PAR turns over with a half-life of <40 s; consistent with significant decrease of NAD+ levels in S phase, which is rescued by PARP inhibitors, in line with the observed rapid turnover of PAR. PARP inhibitors delayed cell cycle in S phase and decreased cell proliferation. Our results underscore the importance of a suitable assay system to measure rapid PAR chain dynamics in living cells and aid our understanding of the function of PARylation during the cell cycle.
Volume 417(1)
Pages 113163
Published 2022-8-1
DOI 10.1016/j.yexcr.2022.113163
PII S0014-4827(22)00156-2
PMID 35447104
MeSH Cell Cycle Cell Division HeLa Cells Humans NAD Poly (ADP-Ribose) Polymerase-1 / genetics Poly (ADP-Ribose) Polymerase-1 / metabolism Poly Adenosine Diphosphate Ribose* / metabolism Poly(ADP-ribose) Polymerase Inhibitors* / pharmacology Poly(ADP-ribose) Polymerases / genetics Poly(ADP-ribose) Polymerases / metabolism
IF 3.383
Resource
Human and Animal Cells HeLa