File S1 - HIF-2α Regulates NANOG Expression in Human Embryonic Stem Cells following Hypoxia and Reoxygenation through the Interaction with an Oct-Sox Cis Regulatory Element

Supporting information. Figure S1, Pluripotency markers are reduced in hESCs cultured at 20% O2 condition compared to hES cells cultured at 5% O2. RT-qPCR analysis of OCT4, SOX2 and NANOG expression in hESCs cultured at 5% or 20% O2. All data have been normalized to UBC and to 1 for 5% O2. Values are mean of 4 independent experiments ± SEM (*P2, 5% O2 or 72 hours post-reoxygenation. Data have been normalized to 5% O2 for hESCs cultured at 20% O2 (A), or either to 20% O2 (B) or 5% O2 (C) for hESCs subjected to reoxygenation. DNA enrichment is expressed as a percentage of input minus the background IgG. An average of 3 to 4 independent experiments is represented (*P2 followed by 72 hours of reoxygenation (Reoxy). Protein expression of HIF-2α (A and B), merged with DAPI (B) and the secondary antibody only negative control (C and D), merged with DAPI (D) of hESCs cultured on Matrigel under hypoxic conditions followed by 72 hours of reoxygenation. Scale bar 25 µm. Figure S4, Expression of HIF-1α in hESCs cultured at 5% O2 for at least 3 passages (5% O2), 5% O2 followed by 72 h of reoxygenation (Reoxy), or 20% O2 followed by 24 hours at 5% O2 (24 h 5% O2). Protein expression of HIF-1α (A–E), merged with DAPI (B, D, F) and the secondary antibody only negative control (G, H), merged with DAPI (H) of hESCs culture at 5% O2 for at least 3 passages (A–B), 5% O2 followed by 72 hours reoxygenation (C–D), or 20% O2 followed by 24 hours at 5% O2 (E–F). Scale bar 25 µm. Table S1, Table S2, Table S3, Table S4. (DOCX)