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Status |
Public on Apr 08, 2020 |
Title |
Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomics [10X_scRNAseq] |
Organism |
Drosophila melanogaster |
Experiment type |
Expression profiling by high throughput sequencing
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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).
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Overall design |
Single-cell RNA-seq data (10X Genomics, Single-cell Expression Solution v2) of the wild type Drosophila third instar larvae eye-antennal disc.
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Contributor(s) |
González-Blas CB, Aerts S |
Citation(s) |
32431014 |
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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
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Organization name |
VIB-KU Leuven
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Department |
VIB-KU Leuven Center for Brain and Disease Research
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Lab |
Laboratory of Computational Biology
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Street address |
Herestraat 49
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City |
Leuven |
ZIP/Postal code |
3000 |
Country |
Belgium |
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Platforms (1) |
GPL21306 |
Illumina HiSeq 4000 (Drosophila melanogaster) |
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Samples (1) |
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This SubSeries is part of SuperSeries: |
GSE141590 |
Identification of genomic enhancers through spatial integration of single-cell transcriptomics and epigenomics |
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Relations |
BioProject |
PRJNA594014 |
SRA |
SRP234988 |