Long-range chromosomal interactions increase and mark repressed gene expression during adipogenesis. Issue 13 (9th December 2022)

• Record Type: Journal Article
• Authors: Garske, Kristina M.; Comenho, Caroline; Pan, David Z.; Alvarez, Marcus; Mohlke, Karen; Laakso, Markku; Pietiläinen, Kirsi H.; Pajukanta, Päivi
• Is Part Of: Epigenetics. Volume 17:Issue 13(2022)
• Page Start: 1849
• Page End: 1862
• Publication Date: 2022-12-09
• Subjects: Adipogenesis -- obesity -- chromosomal interactions; Epigenesis -- Periodicals; Epigenetica; 572.86505
• DOI: 10.1080/15592294.2022.2088145
• Languages: English
• ISSNs: 1559-2294

Abstract

ABSTRACT: Obesity perturbs central functions of human adipose tissue, centred on differentiation of preadipocytes to adipocytes, i.e., adipogenesis. The large environmental component of obesity makes it important to elucidate epigenetic regulatory factors impacting adipogenesis. Promoter Capture Hi-C (pCHi-C) has been used to identify chromosomal interactions between promoters and associated regulatory elements. However, long range interactions (LRIs) greater than 1 Mb are often filtered out of pCHi-C datasets, due to technical challenges and their low prevalence. To elucidate the unknown role of LRIs in adipogenesis, we investigated preadipocyte differentiation to adipocytes using pCHi-C and bulk and single nucleus RNA-seq data. We first show that LRIs are reproducible between biological replicates, and they increase >2-fold in frequency across adipogenesis. We further demonstrate that genomic loci containing LRIs are more epigenetically repressed than regions without LRIs, corresponding to lower gene expression in the LRI regions. Accordingly, as preadipocytes differentiate into adipocytes, LRI regions are more likely to contain repressed preadipocyte marker genes; whereas these same LRI regions are depleted of actively expressed adipocyte marker genes. Finally, we show that LRIs can be used to restrict multiple testing of the long-range cis- eQTL analysis to identify variants that regulate genes via LRIs. We exemplify this by identifying a putative long range cis regulatory mechanism at the LYPLAL1 / TGFB2 obesity locus. In summary, we identify LRIs that mark repressed regions of the genome, and these interactions increase across adipogenesis, pinpointing developmental regions that need to be repressed in a cell-type specific way for adipogenesis to proceed.