Function-based identification of mammalian enhancers using site-specific integration.
Diane E DickelYiwen ZhuAlex S NordJohn N WylieJennifer A AkiyamaVeena AfzalIngrid Plajzer-FrickAileen KirkpatrickBerthold GöttgensBenoit G BruneauAxel ViselLen A PennacchioPublished in: Nature methods (2014)
The accurate and comprehensive identification of functional regulatory sequences in mammalian genomes remains a major challenge. Here we describe site-specific integration fluorescence-activated cell sorting followed by sequencing (SIF-seq), an unbiased, medium-throughput functional assay for the discovery of distant-acting enhancers. Targeted single-copy genomic integration into pluripotent cells, reporter assays and flow cytometry are coupled with high-throughput DNA sequencing to enable parallel screening of large numbers of DNA sequences. By functionally interrogating >500 kilobases (kb) of mouse and human sequence in mouse embryonic stem cells for enhancer activity we identified enhancers at pluripotency loci including NANOG. In in vitro-differentiated cardiomyocytes and neural progenitor cells, we identified cardiac enhancers and neuronal enhancers, respectively. SIF-seq is a powerful and flexible method for de novo functional identification of mammalian enhancers in a potentially wide variety of cell types.
Keyphrases
- single cell
- high throughput
- rna seq
- embryonic stem cells
- flow cytometry
- single molecule
- genome wide
- transcription factor
- endothelial cells
- cell free
- cell therapy
- induced apoptosis
- left ventricular
- stem cells
- small molecule
- dna methylation
- crispr cas
- signaling pathway
- heart failure
- mesenchymal stem cells
- high resolution
- subarachnoid hemorrhage
- bone marrow
- binding protein
- brain injury
- atrial fibrillation
- oxidative stress
- cell cycle arrest
- blood brain barrier
- genetic diversity
- high glucose
- nucleic acid