Study / S3QM2C6N62025-06-12
Rewriting regulatory DNA to dissect and reprogram gene expression
Gabriella E. Martyn, Michael T. Montgomery, Hank Jones, Katherine Guo, Benjamin R. Doughty et al.
About this study
Regulatory DNA provides a platform for transcription factor binding to encode cell-type-specific patterns of gene expression. However, the effects and programmability of regulatory DNA sequences remain difficult to map or predict. Here, we develop variant effects from flow-sorting experiments with CRISPR targeting screens (Variant-EFFECTS) to introduce hundreds of designed edits to endogenous regulatory DNA and quantify their effects on gene expression. We systematically dissect and reprogram 3 regulatory elements for 2 genes in 2 cell types. These data reveal endogenous binding sites with effects specific to genomic context, transcription factor motifs with cell-type-specific activities, and limitations of computational models for predicting the effect sizes of variants. We identify small edits that can tune gene expression over a large dynamic range, suggesting new possibilities for prime-editing-based therapeutics targeting regulatory DNA. Variant-EFFECTS provides a generalizable tool to dissect regulatory DNA and to identify genome editing reagents that tune gene expression in an endogenous context.
Full author list & citation
Gabriella E. Martyn, Michael T. Montgomery, Hank Jones, Katherine Guo, Benjamin R. Doughty, Johannes Linder, Deepa Bisht, Fan Xia, Xiangmeng S. Cai (蔡向濛), Ziwei Chen, Kelly Cochran, Kathryn A. Lawrence, Glen Munson, Anusri Pampari, Charles P. Fulco, Nidhi Sahni, David R. Kelley, Eric S. Lander, Anshul Kundaje, Jesse M. Engreitz. Rewriting regulatory DNA to dissect and reprogram gene expression. 2025-06-12. https://doi.org/10.1016/j.cell.2025.03.034
Experiments 1
E62MMJ31M
A 250-bp hg19 PPIF promoter oligo library spanning -200 to +50 bp relative to the transcription start site, including the wild-type promoter, dinucleotide shuffles, controls, and 353 designed promoter variants, was cloned into the pLS-SceI lentiMPRA vector. The library was assayed in three biological replicates in THP-1 cells, with reporter RNA/DNA barcode ratios and mpralm comparisons to the wild-type promoter used to quantify variant effects.