Contribution of CTCF binding to transcriptional activity at the HOXA locus in NPM1-mutant AML cells

Ghasemi, R.; Struthers, H.; Wilson, E. R.; Spencer, D. H.

doi:10.1101/2020.02.17.952390

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bioRxiv · 10.1101/2020.02.17.952390

Contribution of CTCF binding to transcriptional activity at the HOXA locus in NPM1-mutant AML cells

Ghasemi, R.·Struthers, H.·Wilson, E. R.·Spencer, D. H.

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Abstract

Transcriptional regulation of the HOXA genes is thought to involve CTCF-mediated chromatin loops and the opposing actions of the COMPASS and Polycomb epigenetic complexes. We investigated the role of these mechanisms at the HOXA cluster in AML cells with the common NPM1c mutation, which express both HOXA and HOXB genes. CTCF binding at the HOXA locus is conserved across primary AML samples, regardless of HOXA gene expression, and defines a continuous chromatin domain marked by COMPASS-associated histone H3 trimethylation in NPM1-mutant primary AML samples. Profiling of the three-dimensional chromatin architecture of NPM1-mutant OCI-AML3 cells identified chromatin loops between the active HOXA9-HOXA11 genes and loci in the SNX10 gene and an intergenic region located 1.4Mbp upstream of the HOXA locus. Deletion of CTCF binding sites in OCI-AML3 cells reduced these interactions, but resulted in new, CTCF-independent loops with regions in the SKAP2 gene that were marked by enhancer-associated histone modifications in primary AML samples. HOXA gene expression was maintained in the CTCF deletion mutants, indicating that transcriptional activity at the HOXA locus in NPM1-mutant AML cells does not require long-range CTCF-mediated chromatin interactions, and instead may be driven by intrinsic factors within the HOXA gene cluster.

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Ghasemi, R., Struthers, H., Wilson, E. R., Spencer, D. H.. 2020-02-17. Contribution of CTCF binding to transcriptional activity at the HOXA locus in NPM1-mutant AML cells. https://doi.org/10.1101/2020.02.17.952390

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