Study / S6S00JGJQ2016-06-16
High-throughput functional comparison of promoter and enhancer activities
Thomas A. Nguyen, Richard D. Jones, Andrew R. Snavely, Andreas R. Pfenning, Rory Kirchner et al.
About this study
Promoters initiate RNA synthesis, and enhancers stimulate promoter activity. Whether promoter and enhancer activities are encoded distinctly in DNA sequences is unknown. We measured the enhancer and promoter activities of thousands of DNA fragments transduced into mouse neurons. We focused on genomic loci bound by the neuronal activity-regulated coactivator CREBBP, and we measured enhancer and promoter activities both before and after neuronal activation. We find that the same sequences typically encode both enhancer and promoter activities. However, gene promoters generate more promoter activity than distal enhancers, despite generating similar enhancer activity. Surprisingly, the greater promoter activity of gene promoters is not due to conventional core promoter elements or splicing signals. Instead, we find that particular transcription factor binding motifs are intrinsically biased toward the generation of promoter activity, whereas others are not. Although the specific biases we observe may be dependent on experimental or cellular context, our results suggest that gene promoters are distinguished from distal enhancers by specific complements of transcriptional activators.
Full author list & citation
Thomas A. Nguyen, Richard D. Jones, Andrew R. Snavely, Andreas R. Pfenning, Rory Kirchner, Martin Hemberg, Jesse M. Gray. High-throughput functional comparison of promoter and enhancer activities. 2016-06-16. https://doi.org/10.1101/gr.204834.116
Experiments 3
E1Y7DDY3K
A library of overlapping 139-bp tiles from CREBBP-bound mouse distal enhancers and promoters, with human ortholog controls, was tested in matched enhancer and promoter MPRA reporters. The library was assayed in unstimulated neurons and after KCl depolarization with two biological replicates per condition.
E2JAFR6RN
Synthetic motif and motif-spacing constructs were tested in matched enhancer and promoter MPRA reporters. The library was assayed in unstimulated neurons and after KCl depolarization with three biological replicates per condition; each labeled construct has multiple barcode observations in the deposited tally.
E4TOPPRAZ
Mouse genomic tiles carrying targeted RFX/CREB motif mutations and matched control designs were tested in enhancer and promoter MPRA reporters. The library was assayed in unstimulated and KCl-depolarized neurons with and without an RFX dominant-negative perturbation, using three biological replicates per condition.