Study / S2U73HEUF2019-12-23

Charting the cis-regulome of activated B cells by coupling structural and functional genomics

Virendra K. Chaudhri, Krista Dienger-Stambaugh, Zhiguo Wu, Mahesh Shrestha, Harinder Singh

About this study

Cis-regulomes underlying immune-cell-specific genomic states have been extensively analyzed by structure-based chromatin profiling. By coupling such approaches with a high-throughput enhancer screen (self-transcribing active regulatory region sequencing (STARR-seq)), we assembled a functional cis-regulome for lipopolysaccharide-activated B cells. Functional enhancers, in contrast with accessible chromatin regions that lack enhancer activity, were enriched for enhancer RNAs (eRNAs) and preferentially interacted in vivo with B cell lineage-determining transcription factors. Interestingly, preferential combinatorial binding by these transcription factors was not associated with differential enrichment of their sites. Instead, active enhancers were resolved by principal component analysis (PCA) from all accessible regions by co-varying transcription factor motif scores involving a distinct set of signaling-induced transcription factors. High-resolution chromosome conformation capture (Hi-C) analysis revealed multiplex, activated enhancer-promoter configurations encompassing numerous multi-enhancer genes and multi-genic enhancers engaged in the control of divergent molecular pathways. Motif analysis of pathway-specific enhancers provides a catalog of diverse transcription factor codes for biological processes encompassing B cell activation, cycling and differentiation.

Full author list & citation

Virendra K. Chaudhri, Krista Dienger-Stambaugh, Zhiguo Wu, Mahesh Shrestha, Harinder Singh. Charting the cis-regulome of activated B cells by coupling structural and functional genomics. 2019-12-23. https://doi.org/10.1038/s41590-019-0565-0

Experiments 1

E34LGDAK6

Combined STARR-seq enhancer screen in LPS-activated murine splenic B cells

A standard episomal STARR-seq library of FAIRE-derived genomic fragments was transfected into primary CD43-negative splenic B cells activated with LPS. Public processed data are the authors' combined 12 h/24 h (48 h/60 h transfection, RNA collected at 72 h) STARR-positive peaks overlapping FAIRE peaks, joined where possible to the supplementary enhancer-promoter resource.

Standard STARR-seqMousemm9
Explore data

Raw source data 5 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 5 files (ZIP)41590_2019_565_MOESM2_ESM.xlsxGSE121753_family.soft.gzGSE121753_STARRseq_aB_peaks.bed.gzGSE121753_STARRseq_aB_peaks_overlap_FAIREseqPeaks.bed.gzSOURCES.txt

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