High-throughput functional comparison of promoter and enhancer activities
- Thomas A Nguyen1,
- Richard D Jones1,
- Andrew Snavely1,
- Andreas Pfenning2,
- Rory Kirchner1,
- Martin Hemberg3 and
- Jesse M Gray1,4
- ↵* Corresponding author; email: gray{at}genetics.med.harvard.edu
Abstract
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 co-activator 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, while others are not. While 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.
- Received January 25, 2016.
- Accepted June 14, 2016.
- Published by Cold Spring Harbor Laboratory Press
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