Transcription factor enrichment analysis (TFEA) quantifies the activity of multiple transcription factors from a single experiment

Commun Biol. 2021 Jun 2;4(1):661. doi: 10.1038/s42003-021-02153-7.

Abstract

Detecting changes in the activity of a transcription factor (TF) in response to a perturbation provides insights into the underlying cellular process. Transcription Factor Enrichment Analysis (TFEA) is a robust and reliable computational method that detects positional motif enrichment associated with changes in transcription observed in response to a perturbation. TFEA detects positional motif enrichment within a list of ranked regions of interest (ROIs), typically sites of RNA polymerase initiation inferred from regulatory data such as nascent transcription. Therefore, we also introduce muMerge, a statistically principled method of generating a consensus list of ROIs from multiple replicates and conditions. TFEA is broadly applicable to data that informs on transcriptional regulation including nascent transcription (eg. PRO-Seq), CAGE, histone ChIP-Seq, and accessibility data (e.g., ATAC-Seq). TFEA not only identifies the key regulators responding to a perturbation, but also temporally unravels regulatory networks with time series data. Consequently, TFEA serves as a hypothesis-generating tool that provides an easy, rigorous, and cost-effective means to broadly assess TF activity yielding new biological insights.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Breast / cytology
  • Breast / metabolism
  • Cell Line
  • Chromatin Immunoprecipitation Sequencing / statistics & numerical data
  • Computational Biology / methods
  • Computer Simulation
  • Dexamethasone / pharmacology
  • Epithelial Cells / metabolism
  • Female
  • Gene Expression Regulation
  • Genetic Techniques / statistics & numerical data
  • HCT116 Cells
  • Humans
  • Imidazoles / pharmacology
  • Piperazines / pharmacology
  • Receptors, Glucocorticoid / drug effects
  • Receptors, Glucocorticoid / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Imidazoles
  • Piperazines
  • Receptors, Glucocorticoid
  • TP53 protein, human
  • Transcription Factors
  • Tumor Suppressor Protein p53
  • nutlin 3
  • Dexamethasone