Abstract The mammalian genome is organised into large topologically associating domains (TADs) and smaller sub-TADs or enhancer-promoter loops, which may contribute to the regulation of gene expression. These dynamic structures arise, at least partly, via cohesin-mediated loop extrusion delimited by insulator elements. By studying the structure and function of the alpha-globin locus during erythroid differentiation, we have previously shown that the juxtaposition of the enhancers and promoters during this process partly depends on cohesin-mediated loop extrusion, which appears to be delimited by 12 largely convergently orientated CTCF boundary elements. To define the downstream boundary of the sub-TAD, we removed four CTCF sites in informative combinations. This showed that rather than CTCF insulators, it is the transcriptionally active alpha-globin gene that defines the downstream boundary of the sub-TAD. Further, insertion of actively transcribed fragments of the α-globin gene between the enhancers and native genes leads to a reduction in native α-globin expression and accumulation of cohesin at the insertion site. This highlights an overlap in the functional role of the fundamental elements of the genome.
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Lucy Cornell
University of Oxford
Caroline L. Harrold
John Radcliffe Hospital
Susannah Holliman
University of Oxford
The EMBO Journal
University of Oxford
The Francis Crick Institute
Science Oxford
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Cornell et al. (Mon,) studied this question.
synapsesocial.com/papers/69ba421b4e9516ffd37a2031 — DOI: https://doi.org/10.1038/s44318-026-00730-2