Reversing the TERT promoter mutation to WT reverses the active chromatin marks and alters long-range chromatin interactions. Reversing the TERT promoter.

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Reversing the TERT promoter mutation to WT reverses the active chromatin marks and alters long-range chromatin interactions. Reversing the TERT promoter mutation to WT reverses the active chromatin marks and alters long-range chromatin interactions. A, CRISPR/Cas9-mediated reversal strategy of mutated -146C>T residue (shown as red color) to WT -146C residue (shown as orange color) by repair template harboring -146C residue. We obtained BLM cells that have undergone the CRISPR process and are mutant for -146C residue and are labeled as BLM6. BLM cells that have undergone the CRISPR process and mutated back to WT for -146T residue to -146C residue are labeled as BLM14. B, DNA chromatograms spanning the TERT promoter region in BLM6 and BLM14 are shown. ChIP was performed in BLM6 and BLM14 cells against histone marks (H3K4Me3 and H3K9Ac). Graph shows qPCR analysis with % input obtained across various regions of TERT promoter with distances indicated in boxes below the x axis. Error bars indicate the mean ± SD of the two independent experiments. P values were calculated by two-tailed Student t test method. C–E, plot generated by FourCSeq of the differential intrachromosomal interactions of the TERT promoter between replicates of BLM6 and BLM14. The green line shows the distance-dependent fit and the blue dashed line indicates the fit of z-score > 2. Interactions detected by z-score > 2 (P-adjusted value < 0.05) for at least one replicate are shown as red dots. Fragments not called as interactions and that do not show significant change between conditions are shown as black dots. vst, variance stabilizing transformation. E, the calculated log2 fold change is shown above the hg 19 RefSeq genes in the regions 1 megabase from the TERT promoter. F, quantifications of 5 interactions, obtained from C–E, were measured by 3C-qPCR in BLM6 cells. G, quantification of TERT promoter interaction with 300 kb upstream (chr5:1,556,087–1,558,758) DNA region (T-INT1) measured by 3C-qPCR in BLM6 and BLM14 cells. Error bars indicate the mean ± SD of the three independent experiments. P values were calculated by two-tailed Student t test method. Semih Can Akıncılar et al. Cancer Discov 2016;6:1276-1291 ©2016 by American Association for Cancer Research