Identification of drug responsive enhancers by predicting chromatin accessibility change from perturbed gene expression profiles.
Yongcui WangYong WangPublished in: NPJ systems biology and applications (2024)
Individual may response to drug treatment differently due to their genetic variants located in enhancers. These variants can alter transcription factor's (TF) binding strength, affect enhancer's chromatin activity or interaction, and eventually change expression level of downstream gene. Here, we propose a computational framework, PERD, to Predict the Enhancers Responsive to Drug. A machine learning model was trained to predict the genome-wide chromatin accessibility from transcriptome data using the paired expression and chromatin accessibility data collected from ENCODE and ROADMAP. Then the model was applied to the perturbed gene expression data from Connectivity Map (CMAP) and Cancer Drug-induced gene expression Signature DataBase (CDS-DB) and identify drug responsive enhancers with significantly altered chromatin accessibility. Furthermore, the drug responsive enhancers were related to the pharmacogenomics genome-wide association studies (PGx GWAS). Stepping on the traditional drug-associated gene signatures, PERD holds the promise to enhance the causality of drug perturbation by providing candidate regulatory element of those drug associated genes.
Keyphrases
- genome wide
- gene expression
- transcription factor
- drug induced
- dna methylation
- adverse drug
- copy number
- machine learning
- dna damage
- electronic health record
- emergency department
- big data
- cancer therapy
- squamous cell carcinoma
- poor prognosis
- drug delivery
- single cell
- oxidative stress
- quantum dots
- dna binding
- deep learning
- rna seq
- genome wide association
- clinical decision support