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Series GSE122026 Query DataSets for GSE122026
Status Public on Dec 27, 2018
Title Dermal Condensate Niche Fate Specification Occurs Prior to Formation and Is Placode Progenitor Dependent
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Cell fate transitions are essential for specification of stem cells and their niches, but the precise timing and sequence of molecular events during embryonic development are largely unknown. Here, we identify with 3D/4D microscopy unclustered precursors of dermal condensates (DC), signaling niches for epithelial progenitors in hair placodes. With population-based and single-cell transcriptomics, we define a molecular time-lapse from pre-DC fate specification through DC niche formation and establish the developmental trajectory as the DC lineage emerges from fibroblasts. Co-expression of downregulated fibroblast and upregulated DC genes in niche precursors reveals a transitory molecular state following a proliferation shutdown. Waves of transcription factor and signaling molecule expression then coincide with DC formation. Finally, ablation of epidermal Wnt signaling and placode-derived FGF20 demonstrates their requirement for pre-DC specification. These findings uncover a progenitor-dependent niche precursor fate and the transitory molecular events controlling niche formation and function.
 
Overall design Dorsal skins were dissected from E15.0 embryos, dissociated into single cells, and FACS sorted. Single-cell transcriptomics was performed on live cells using an automated version of CEL-seq2 on live, FACS sorted cells. The StemID algorithm was used to identify clusters of cells corresponding to stages of DC development, starting from fibroblasts.

Bulk RNA-sequencing of sorted populations from E15.0 backskin; raw data files contain all transcriptome information for pre-DC, DC1, DC2, fibroblasts, Schwann cells, and negative population, processed data file includes transcriptome information for pre-DC, DC1, DC2, fibroblasts, Schwann cells and negative population used in this study.

Single Cell RNA-sequencing of E15.0 mouse backskin; raw data files contain all single cell transcriptome information, processed data file includes mesenchymal transcriptome information used in this study.
Web link https://www.sciencedirect.com/science/article/pii/S1534580718310177?via%3Dihub
 
Contributor(s) Mok K, Saxena N, Heitman N, Grisanti L, Srivastava D, Muraro M, Jacob T, Sennett R, Wang Z, Su Y, Yang L, Ma'ayan A, Ornitz D, Kasper M, Rendl M
Citation(s) 30595537
NIH grant(s)
Grant ID Grant title Affiliation Name
R01 AR063151 Exploring How Dermal Papilla Precursors Regulate Hair Follicle Formation MOUNT SINAI SCHOOL OF MEDICINE Michael Rendl
R01 AR071047 Specification and Molecular Control of the Hair Follicle Inductive Mesenchyme MOUNT SINAI SCHOOL OF MEDICINE Michael Rendl
Submission date Oct 31, 2018
Last update date Mar 28, 2019
Contact name Michael Rendl
E-mail(s) michaelrendl@gmail.com
Organization name Mount Sinai School of Medicine
Street address 1428 Madison Avenue
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platforms (2)
GPL13112 Illumina HiSeq 2000 (Mus musculus)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (21)
GSM3453131 Bulk_pre-DC_rep1 [291_AACCAG]
GSM3453132 Bulk_pre-DC_rep2 [307_AAGAGG]
GSM3453133 Bulk_DC1_rep1 [295_GCACTA]
Relations
BioProject PRJNA503184
SRA SRP167339

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Supplementary file Size Download File type/resource
GSE122026_E15.0_Mesenchymal_cells_scRNAseq_Final.csv.gz 8.0 Mb (ftp)(http) CSV
GSE122026_E15.0_bulkRNAseq_Final.xlsx 3.4 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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