Study / S2HH2HD5L2015-04-15

High-throughput and quantitative assessment of enhancer activity in mammals by CapStarr-seq

Laurent Vanhille, Aurélien Griffon, Muhammad Ahmad Maqbool, Joaquin Zacarias-Cabeza, Lan T.M. Dao et al.

About this study

Cell-type specific regulation of gene expression requires the activation of promoters by distal genomic elements defined as enhancers. The identification and the characterization of enhancers are challenging in mammals due to their genome complexity. Here we develop CapStarr-Seq, a novel high-throughput strategy to quantitatively assess enhancer activity in mammals. This approach couples capture of regions of interest to previously developed Starr-seq technique. Extensive assessment of CapStarr-seq demonstrates accurate quantification of enhancer activity. Furthermore, we find that enhancer strength is associated with binding complexity of tissue-specific transcription factors and super-enhancers, while additive enhancer activity isolates key genes involved in cell identity and function. The CapStarr-Seq thus provides a fast and cost-effective approach to assess the activity of potential enhancers for a given cell type and will be helpful in decrypting transcription regulation mechanisms.

Full author list & citation

Laurent Vanhille, Aurélien Griffon, Muhammad Ahmad Maqbool, Joaquin Zacarias-Cabeza, Lan T.M. Dao, Nicolas Fernandez, Benoit Ballester, Jean Christophe Andrau, Salvatore Spicuglia. High-throughput and quantitative assessment of enhancer activity in mammals by CapStarr-seq. 2015-04-15. https://doi.org/10.1038/ncomms7905

Experiments 2

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CapStarr-seq enhancer activity in the P5424 mouse T-cell line

A targeted CapStarr-seq library captured approximately 400-bp fragments spanning 7,542 candidate mouse cis-regulatory modules (CRMs) and was transfected into the P5424 immature T-cell line. The table retains the authors' 7,152 input-qualified candidate CRMs plus the 69 published CTCF-bound control regions, with two P5424 biological replicate scores and the merged enhancer score where available.

Targeted / Cap-STARR-seqMousemm9
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CapStarr-seq enhancer activity in NIH-3T3 mouse fibroblasts

The same targeted CapStarr-seq library of approximately 7,542 mouse candidate CRMs was transfected into NIH-3T3 fibroblasts as a non-lymphoid control condition. The table contains the 7,152 candidate CRMs passing the source input-library capture filter, with NIH-3T3 fold-change activity and the authors' activity class.

Targeted / Cap-STARR-seqMousemm9
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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)GSE60029_family.soft.gzGSE60029_RAW.tarGSE60029_series_matrix.txt.gzsupplementary_data_1_crms.xlssupplementary_data_2_ctcf.xlssupplementary_data_3_luciferase.xlssupplementary_data_4_hal.xlssupplementary_figures_tables.pdf

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