Super-enhancers require a combination of classical enhancers and novel facilitator elements to drive high levels of gene expression
Year: 2022
Type: preprint
Abstract: Super-enhancers (SEs) are a class of compound regulatory elements which control expression of key cell-identity genes. It remains unclear whether they are simply clusters of independent classical enhancers or whether SEs manifest emergent properties and should therefore be considered as a distinct class of element. Here, using synthetic biology and genome editing, we engineered the well characterised erythroid α-globin SE at the endogenous α-globin locus, removing all SE constituent elements in a mouse embryonic stem cell-line, to create a “blank canvas”. This has allowed us to re-build the SE through individual and combinatorial reinsertion of its five elements (R1, R2, R3, Rm, R4), to test the importance of each constituent’s sequence and position within the locus. Each re-inserted element independently creates a region of open chromatin and binds its normal repertoire of transcription factors; however, we found a high degree of functional interdependence between the five constituents. Surprisingly, the two strongest α-globin enhancers (R1 and R2) act sub-optimally both on their own and in combination, and although the other three elements (R3, Rm and R4) exhibit no discernible enhancer activity, they each exert a major positive effect in facilitating the activity of the classical enhancers (R1 and R2). This effect depends not simply on the sequence of each element but on their positions within the cluster. We propose that these “facilitators” are a novel form of regulatory element, important for ensuring the full activity of SEs, but distinct from conventional enhancer elements.
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: green
Awards: Proximity to Discovery - University of Oxford, MICA: Nanoscopy Oxford (NanO): Novel Super-Resolution Imaging Applied to Biomedical Sciences, Developing an initiative in stem cell editing for human genetic diseases., Global Study of Thalassaemia, Functional dissection of a single enhancer sequence at the mouse a-globin locus, The regulation of globin gene expression during haematopoiesis, Studying gene expression regulation at the alpha-globin locus, MRC/AZ CLD 2018, The Oxford Single Cell Biology Consortium, Rebuilding a superenhancer to investigate the additive and synergistic effects of its individual components, G6868616705, Oxford, Chromosome and Developmental Biology., Switching mammalian genes on and off during development, lineage specification, and differentiation, and its impact on human genetic disease, Studying gene expression regulation at the alpha-globin locus, Rebuilding a superenhancer to investigate the additive and synergistic effects of its individual components
OpenAlex ID: W4283268517
