Cell Genomics (Feb 2022)

CASCADE: high-throughput characterization of regulatory complex binding altered by non-coding variants

  • David Bray,
  • Heather Hook,
  • Rose Zhao,
  • Jessica L. Keenan,
  • Ashley Penvose,
  • Yemi Osayame,
  • Nima Mohaghegh,
  • Xiaoting Chen,
  • Sreeja Parameswaran,
  • Leah C. Kottyan,
  • Matthew T. Weirauch,
  • Trevor Siggers

Journal volume & issue
Vol. 2, no. 2
p. 100098

Abstract

Read online

Summary: Non-coding DNA variants (NCVs) impact gene expression by altering binding sites for regulatory complexes. New high-throughput methods are needed to characterize the impact of NCVs on regulatory complexes. We developed CASCADE (Customizable Approach to Survey Complex Assembly at DNA Elements), an array-based high-throughput method to profile cofactor (COF) recruitment. CASCADE identifies DNA-bound transcription factor-cofactor (TF-COF) complexes in nuclear extracts and quantifies the impact of NCVs on their binding. We demonstrate CASCADE sensitivity in characterizing condition-specific recruitment of COFs p300 and RBBP5 (MLL subunit) to the CXCL10 promoter in lipopolysaccharide (LPS)-stimulated human macrophages and quantify the impact of all possible NCVs. To demonstrate applicability to NCV screens, we profile TF-COF binding to ∼1,700 single-nucleotide polymorphism quantitative trait loci (SNP-QTLs) in human macrophages and identify perturbed ETS domain-containing complexes. CASCADE will facilitate high-throughput testing of molecular mechanisms of NCVs for diverse biological applications.

Keywords