VISION
VISION integrates epigenomic datasets from mouse and human hematopoietic cells to map regulatory landscapes and elucidate how GATA1, GATA2, GATA3 and Ikaros transcription factors govern hematopoiesis.
Key Features:
- Epigenomic Data Integration: Incorporates nuclease accessibility, CTCF occupancy, and histone H3 modifications across twenty distinct cell types including hematopoietic stem cells, multilineage progenitors, and mature blood lineage cells from mouse and human.
- IDEAS Framework: Employs the Integrative and Discriminative Epigenome Annotation System (IDEAS) to analyze data along chromosomes and across cell types, learning common combinations of epigenetic features to segment the genome.
- Regulatory Landscape Mapping: Identifies constitutively active or silent loci and loci specifically induced or repressed across hematopoietic stages and lineages.
- Candidate Regulatory Elements Identification: Designates nuclease-accessible DNA segments within active chromatin states as candidate cis-regulatory elements for each cell type, yielding a comprehensive registry of hematopoietic candidate regulatory elements.
Scientific Applications:
- GATA and Ikaros regulation: Facilitates analysis of how GATA1, GATA2, GATA3, and Ikaros transcription factors interact with the epigenome to regulate target genes.
- Hematopoietic differentiation: Supports investigation of regulatory mechanisms driving hematopoietic differentiation and lineage-specific gene expression.
Methodology:
Uses IDEAS to learn common combinations of epigenetic states simultaneously across chromosomes and cell types and to produce a genome segmentation representing regulatory states.
Topics
Details
- Added:
- 11/14/2019
- Last Updated:
- 1/2/2021
Operations
Publications
Hardison RC, Zhang Y, Keller CA, Xiang G, Heuston E, An L, Lichtenberg J, Giardine BM, Bodine D, Mahony S, Li Q, Yue F, Weiss MJ, Blobel G, Taylor J, Hughes J, Higgs D, Gottgens B. Systematic integration of GATA transcription factors and epigenomes via IDEAS paints the regulatory landscape of mouse hematopoietic cells. Unknown Journal. 2019. doi:10.1101/730358.