Study / S61MD61G22024-10-28
Large-scale analysis of the integration of enhancer-enhancer signals by promoters
Miguel Martinez-Ara, Federico Comoglio, Bas van Steensel
About this study
Genes are often regulated by multiple enhancers. It is poorly understood how the individual enhancer activities are combined to control promoter activity. Anecdotal evidence has shown that enhancers can combine sub-additively, additively, synergistically, or redundantly. However, it is not clear which of these modes are more frequent in mammalian genomes. Here, we systematically tested how pairs of enhancers activate promoters using a three-way combinatorial reporter assay in mouse embryonic stem cells. By assaying about 69,000 enhancer-enhancer-promoter combinations we found that enhancer pairs generally combine near-additively. This behaviour was conserved across seven developmental promoters tested. Surprisingly, these promoters scale the enhancer signals in a non-linear manner that depends on promoter strength. A housekeeping promoter showed an overall different response to enhancer pairs, and a smaller dynamic range. Thus, our data indicate that enhancers mostly act additively, but promoters transform their collective effect non-linearly.
Full author list & citation
Miguel Martinez-Ara, Federico Comoglio, Bas van Steensel. Large-scale analysis of the integration of enhancer-enhancer signals by promoters. 2024-10-28. https://doi.org/10.7554/eLife.91994
Experiments 8
E18MWATTA
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Fgf5 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E191N75VX
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Nanog promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E1SNTM95V
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Sox2 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E3GVBJD1S
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Lefty1 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E7LR8XMFT
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Otx2 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E8ES8J8AP
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Tbx3 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E9LUJXDXY
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Klf2 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.
E9XX24XAC
One of eight promoter-specific libraries in the three-way enhancer-enhancer-promoter (EEP) MPRA, using the Ap1m1 promoter with pairs of approximately 450 bp mouse regulatory elements or synthetic controls. The library was transiently transfected separately into E14TG2a mouse embryonic stem cells, and reporter cDNA/pDNA barcode ratios were summarized across three biological replicates.