RT Journal Article
SR Electronic
T1 γ-H2AX - A Novel Biomarker for DNA Double-strand Breaks
JF In Vivo
JO In Vivo
FD International Institute of Anticancer Research
SP 305
OP 309
VO 22
IS 3
A1 LINDA J. KUO
A1 LI-XI YANG
YR 2008
UL http://iv.iiarjournals.org/content/22/3/305.abstract
AB When DNA damage, whether it is endogenous or exogenous, forms double stranded breaks (DSBs), it is always followed by the phosphorylation of the histone, H2AX. H2AX is a variant of the H2A protein family, which is a component of the histone octomer in nucleosomes. It is phosphorylated by kinases such as ataxia telangiectasia mutated (ATM) and ATM-Rad3-related (ATR) in the PI3K pathway. This newly phosphorylated protein, γ-H2AX, is the first step in recruiting and localizing DNA repair proteins. DSBs can be induced by mechanisms such as ionizing radiation or cytotoxic agents and subsequently, γ-H2AX foci quickly form. These foci represent the DSBs in a 1:1 manner and can be used as a biomarker for damage. An antibody can be raised against γ-H2AX which can therefore be visualized by immunofluorescence through secondary antibodies. The detection and visualization of γ-H2AX by flow cytometry allow the assessment of DNA damage, related DNA damage proteins and DNA repair. γ-H2AX also has other applications in the detection of genomic damage caused by cytotoxic chemical agents and environmental and physical damage, especially in the context of cancer treatment and therapy.