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Series GSE141580 Query DataSets for GSE141580
Status Public on Apr 08, 2020
Title Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomics [FluidigmC1_scATACseq]
Organism Drosophila melanogaster
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Enhancers act as docking stations in the genome to which transcription factors bind, tightly regulating gene expression. Although single-cell technologies allow measuring chromatin accessibility or gene expression in each individual cell, exploiting both layers towards bona fide gene regulatory networks and enhancers is still a challenge. Here, we independently generate comprehensive single-cell transcriptome and epigenome atlases of the Drosophila eye-antennal disc and propose the spatial integration of single-cell RNA-seq and single-cell ATAC-seq data using a virtual latent space that mimics the spatial organization of the 2D tissue. To validate spatially predicted enhancers, we use a large collection of enhancer-reporter lines and identify ~85% of enhancers for which chromatin accessibility and enhancer activity patterns agree; while the remaining ~15% are ubiquitously accessible regions bound by the pioneer transcription factor Grainyhead, for which accessibility and activity do not correlate. Next, we infer linear and non-linear enhancer-to-target gene relationships in the virtual space, and find that genes are mostly regulated by multiple -and in some cases, redundant - enhancers. In addition, using cell-type specific enhancers learned from the scATAC-seq data, we deconvolute the cell-type specific effects of chromatin accessibility QTLs from a panel of 50 bulk ATAC-seq profiles from Drosophila inbred lines. Finally, we identify Prospero as a key transcription factor driving neuronal photoreceptor differentiation through the binding of a GGG recognition motif. In summary, we provide a comprehensive spatial characterization of gene regulation in a 2D tissue, which can be explored via SCope (http://scope.aertslab.org/#/Bravo_et_al_EyeAntennalDisc) and the UCSC Genome browser (http://genome.ucsc.edu/s/cbravo/Bravo_et_al_EyeAntennalDisc).
 
Overall design Single-cell ATAC-seq data (Fluidigm C1) of sens-GFP+ cells from the wild type Drosophila third instar larvae eye-antennal disc.
 
Contributor(s) González-Blas CB, Aerts S
Citation(s) 32431014
Submission date Dec 06, 2019
Last update date May 26, 2020
Contact name Carmen Bravo González-Blas
E-mail(s) carmen.bravogonzalezblas@kuleuven.vib.be
Organization name VIB-KU Leuven
Department VIB-KU Leuven Center for Brain and Disease Research
Lab Laboratory of Computational Biology
Street address Herestraat 49
City Leuven
ZIP/Postal code 3000
Country Belgium
 
Platforms (1)
GPL19132 Illumina NextSeq 500 (Drosophila melanogaster)
Samples (384)
GSM4208785 FLUIDIGMC1_SCATACSEQ_SENS-GFP_CELL_1
GSM4208786 FLUIDIGMC1_SCATACSEQ_SENS-GFP_CELL_2
GSM4208787 FLUIDIGMC1_SCATACSEQ_SENS-GFP_CELL_3
This SubSeries is part of SuperSeries:
GSE141590 Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomics
Relations
BioProject PRJNA594010
SRA SRP234982

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Supplementary file Size Download File type/resource
GSE141580_FLUIDIGMC1_SCATACSEQ_SENS-GFP_AGGREGATE.normalized.bw 2.7 Mb (ftp)(http) BW
GSE141580_FLUIDIGMC1_SCATACSEQ_SENS-GFP_CTXREGIONS.tsv.gz 923.1 Kb (ftp)(http) TSV
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Raw data are available in SRA
Processed data are available on Series record

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