Deep-transcriptome and ribonome sequencing redefines the molecular networks of pluripotency and the extracellular space in human embryonic stem cells

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 4.
Figure 4.

Enrichment of genes and alternative variants in the M/S enriched fraction. (A) Marked spatial separation of genes expressed in the membrane/secreted (M/S) and cytoplasmic/nuclear (C/N) fractions. The histogram shows frequency of genes expressed (RPKM > 1) plotted against the log2 ratio of M/S expression to C/N expression, log2(RPKMM/S/RPKMC/N). (B) Graph showing the correlation between canonical gene expression (x-axis) and expression of the novel annotated sequence (3′ UTR, 5′ UTR, intron retention; y-axis) for a subset of M/S genes. Notably, correlation with canonical gene expression is high for 3′ UTRs. (C) UCSC Genome Browser view of four genes for which novel long 3′ UTRs were detected by RNA-seq. Each track shows the log2 ratio of M/S to C/N expression calculated at 50-bp windows across the gene for the positive strand. (Orange) M/S-enriched regions; (blue) regions not enriched in M/S. Note the consistency of the M/S to C/S ratio across annotated 3′ UTRs, continuing through the length of the predicted novel 3′UTR.

This Article

  1. Genome Res. 21: 2014-2025

Preprint Server