[HTML][HTML] Quantification of cell cycle kinetics by EdU (5-ethynyl-2′-deoxyuridine)-coupled-fluorescence-intensity analysis

PD Pereira, A Serra-Caetano, M Cabrita, E Bekman… - Oncotarget, 2017 - ncbi.nlm.nih.gov
PD Pereira, A Serra-Caetano, M Cabrita, E Bekman, J Braga, J Rino, R Santus, PL Filipe…
Oncotarget, 2017ncbi.nlm.nih.gov
We propose a novel single-deoxynucleoside-based assay that is easy to perform and
provides accurate values for the absolute length (in units of time) of each of the cell cycle
stages (G1, S and G2/M). This flow-cytometric assay takes advantage of the excellent
stoichiometric properties of azide-fluorochrome detection of DNA substituted with 5-ethynyl-
2′-deoxyuridine (EdU). We show that by pulsing cells with EdU for incremental periods of
time maximal EdU-coupled fluorescence is reached when pulsing times match the length of …
Abstract
We propose a novel single-deoxynucleoside-based assay that is easy to perform and provides accurate values for the absolute length (in units of time) of each of the cell cycle stages (G1, S and G2/M). This flow-cytometric assay takes advantage of the excellent stoichiometric properties of azide-fluorochrome detection of DNA substituted with 5-ethynyl-2′-deoxyuridine (EdU). We show that by pulsing cells with EdU for incremental periods of time maximal EdU-coupled fluorescence is reached when pulsing times match the length of S phase. These pulsing times, allowing labelling for a full S phase of a fraction of cells in asynchronous populations, provide accurate values for the absolute length of S phase. We characterized additional, lower intensity signals that allowed quantification of the absolute durations of G1 and G2 phases.
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