Study / S2PJ2JX3O2014-06-08

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.

About this study

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

Experiments 2

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Genome-wide S2 STARR-seq enhancer activity across five Drosophila species

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.

Whole-Genome STARR-seq (WHG-STARR-seq)Fruit flydm3
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E7FQW1RZS

Genome-wide OSC STARR-seq enhancer activity across three Drosophila species

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.

Whole-Genome STARR-seq (WHG-STARR-seq)Fruit flydm3
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Raw source data 8 files

Original supplemental and deposited inputs retained for this study. Download files individually or together as a ZIP; nested folders are preserved. Source reuse terms apply, and sequencing reads may be omitted.

Download all 8 files (ZIP)GSE40739_family.soft.gzGSE40739_RAW.tarGSE48251_family.soft.gzGSE48251_RAW.tarNIHMS644080-supplement-Supplementary_Materials.pdfREADME.txtSupplementary_Data_Set_1.zipTableS02.xlsx

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