Cis-Regulatory Atlas in Primary Human CD4+ T Cells

Abstract

Cis–regulatory elements (CRE) are critical for coordinating gene expression programs that dictate cell–specific differentiation and homeostasis. Recently developed self–transcribing active regulatory region sequencing (STARR–Seq) has allowed for genome-wide annotation of functional CREs. Despite this, STARR–Seq assays are only employed in cell lines, in part, due to difficulties in delivering reporter constructs. Herein, we implemented and validated a STARR–Seq–based screen in human CD4+ T cells using a non–integrating lentiviral transduction system. Lenti–STARR–Seq is the first example of a genome–wide assay of CRE function in human primary cells, identifying thousands of functional enhancers and negative regulatory elements (NREs) in human CD4+ T cells. Results of the screen were validated using traditional luciferase assays. Genome-wide, we find clear differences between enhancers and NREs in nucleosome positioning, chromatin modification, eRNA production, and transcription factor binding. Our findings support the idea of silencer repurposing as enhancers in alternate cell types. Collectively, these data suggest that Lenti–STARR–Seq is a can be used for CRE screening in primary human cell types.