Lucy J Cornell,Caroline L Harrold,Susannah Holliman,Felice Tsang,Matthew E Gosden,Lars L P Hanssen,Rosa Stolper,Damien J Downes,Daniel Biggs,Chris Preece,Samy Alghadban,Jacqueline A Sharpe,Benjamin Davies,Jacqueline A Sloane-Stanley,Jim R Hughes,Douglas R Higgs,Mira T Kassouf
{"title":"A functional overlap between actively transcribed genes and chromatin insulator elements.","authors":"Lucy J Cornell,Caroline L Harrold,Susannah Holliman,Felice Tsang,Matthew E Gosden,Lars L P Hanssen,Rosa Stolper,Damien J Downes,Daniel Biggs,Chris Preece,Samy Alghadban,Jacqueline A Sharpe,Benjamin Davies,Jacqueline A Sloane-Stanley,Jim R Hughes,Douglas R Higgs,Mira T Kassouf","doi":"10.1038/s44318-026-00730-2","DOIUrl":null,"url":null,"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.","PeriodicalId":501009,"journal":{"name":"The EMBO Journal","volume":"94 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-03-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The EMBO Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s44318-026-00730-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
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.