Quantitative genome-wide enhancer activity maps for five Drosophila species show functional enhancer conservation and turnover during cis-regulatory evolution
Cosmas D Arnold, Daniel Gerlach, Daniel Spies, Jessica A Matts, Yuliya A Sytnikova et al.
Phenotypic differences between closely related species are thought to arise primarily from changes in gene expression due to mutations in cis-regulatory sequences (enhancers). However, it has remained unclear how frequently mutations alter enhancer activity or create functional enhancers de novo. Here we use STARR-seq, a recently developed quantitative enhancer assay, to determine genome-wide enhancer activity profiles for five Drosophila species in the constant trans-regulatory environment of Drosophila melanogaster S2 cells. We find that the functions of a large fraction of D. melanogaster enhancers are conserved for their orthologous sequences owing to selection and stabilizing turnover of transcription factor motifs. Moreover, hundreds of enhancers have been gained since the D. melanogaster-Drosophila yakuba split about 11 million years ago without apparent adaptive selection and can contribute to changes in gene expression in vivo. Our finding that enhancer activity is often deeply conserved and frequently gained provides functional insights into regulatory evolution.
Full author list & citation
Cosmas D Arnold, Daniel Gerlach, Daniel Spies, Jessica A Matts, Yuliya A Sytnikova, Michaela Pagani, Nelson C Lau, Alexander Stark. Quantitative genome-wide enhancer activity maps for five Drosophila species show functional enhancer conservation and turnover during cis-regulatory evolution. 2014-06-08. https://doi.org/10.1038/ng.3009
Genomic DNA from D. melanogaster, D. yakuba, D. ananassae, D. pseudoobscura, and D. willistoni was screened in the same D. melanogaster S2 cell trans-regulatory environment. The table contains the study's combined two-biological-replicate enhancer peak calls after translation to dm3-compatible coordinates.
Genomic DNA from D. melanogaster, D. yakuba, and D. ananassae was screened in D. melanogaster ovarian somatic cells (OSCs), a common trans-regulatory environment. The table contains the study's combined two-biological-replicate enhancer peak calls after translation to dm3-compatible coordinates.
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