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. 2016 May 31;36(12):1764–1775. doi: 10.1128/MCB.01098-15

FIG 1.

FIG 1

lncRHOXF1 is robustly expressed during early human development. (A) Schematic showing RNA sequencing reads (RPKM) for lncRHOXF1 during early human development (14). (B) Genomic location of lncRHOXF1 on the X chromosome. XIC, X-inactivation center. Primer locations for transcript cloning (F1 and R4) and qPCR (F1 and R2) are shown. (C) Bright-field images of a human embryonic stem cell colony cultured using mouse embryonic fibroblasts (left) and BMP4/A/P-differentiated cells after 9 days (right). (D) qRT-PCR analysis of decreased NANOG expression during BMP4/A/P differentiation. Error bars denote standard deviations from the means. (E) qRT-PCR analysis of increased placentation markers CDX2 and hCG-α expression during BMP4/A/P differentiation. Error bars denote standard deviations from the means. (F) RT-PCR amplification of exons 1 to 4 of lncRHOXF1 by using primers F1 and R4 and RNA from BMP4/A/P-differentiated hESCs. (G) qRT-PCR analysis of lncRHOXF1 expression in male hESCs (blue) and hiPSCs (green) during BMP4/A/P differentiation. Error bars denote standard deviations from the mean. (H) qRT-PCR analysis of lncRHOXF1 expression during BMP4/A/P differentiation of human female pluripotent stem cells. Error bars denote standard deviations from the means.