Study / S3G8Z00ZL2021-09-06
Information content differentiates enhancers from silencers in mouse photoreceptors
Ryan Z. Friedman, David M. Granas, Connie A. Myers, Joseph C. Corbo, Barak A. Cohen et al.
About this study
Enhancers and silencers often depend on the same transcription factors (TFs) and are conflated in genomic assays of TF binding or chromatin state. To identify sequence features that distinguish enhancers and silencers, we assayed massively parallel reporter libraries of genomic sequences targeted by the photoreceptor TF cone-rod homeobox (CRX) in mouse retinas. Both enhancers and silencers contain more TF motifs than inactive sequences, but relative to silencers, enhancers contain motifs from a more diverse collection of TFs. We developed a measure of information content that describes the number and diversity of motifs in a sequence and found that, while both enhancers and silencers depend on CRX motifs, enhancers have higher information content. The ability of information content to distinguish enhancers and silencers targeted by the same TF illustrates how motif context determines the activity of cis-regulatory sequences.
Full author list & citation
Ryan Z. Friedman, David M. Granas, Connie A. Myers, Joseph C. Corbo, Barak A. Cohen, Michael A. White. Information content differentiates enhancers from silencers in mouse photoreceptors. 2021-09-06. https://doi.org/10.7554/eLife.67403
Experiments 2
E0DHJKB2U
Two 2,422-element libraries of 164-bp mouse genomic sequences, CRX-site mutants, shape mutants, and scrambled controls were cloned upstream of the basal rod photoreceptor Rhodopsin (Rho) promoter and DsRed. Each library was electroporated into explanted P0 CD-1 mouse retinas in three biological replicates, harvested at P8, and quantified by reporter cDNA versus input-plasmid DNA barcode sequencing.
E4BUO215G
The same two 2,422-element libraries were recloned with a minimal 23-bp polylinker in place of the basal Rho promoter and assayed in explanted P0 CD-1 mouse retinas. Three biological replicates per library were quantified by reporter cDNA versus input-plasmid DNA barcode sequencing; activity above the DNA-normalized baseline was treated as autonomous activity.