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Status |
Public on Apr 28, 2016 |
Title |
Sp7/Osterix is restricted to bone-forming vertebrates where it acts as a Dlx co-factor in osteoblast specification [RNA-Seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Sp7/Osterix is a master regulator of osteoblast specification. To identify transcripts profile in Sp7 positive osteoblast, we performed RNA-seq on primary mouse calvarial cells obtained from Sp7-GFP reporter mice at P1. By hierarchical clustering using transcriptional profiles for chondrocytes and mouse embryonic fibroblasts (MEFs) together with the osteoblast data, we identified cell-type enriched gene expression signatures in osteoblasts, chondrocytes and MEFs. In conjunction with Sp7 ChIP-seq in osteoblast, we identified putative Sp7 targets which underlie the osteoblast regulatory program.
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Overall design |
RNA-seq experiments with GFP-sorted Sp7 positive osteoblasts and chondrocytes isolated from wild-type rib cartilage at P1
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Contributor(s) |
Hojo H, Ohba S, He X, Lai LP, McMahon AP |
Citation(s) |
27134141 |
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Submission date |
Dec 20, 2015 |
Last update date |
Jun 16, 2021 |
Contact name |
Hironori Hojo |
E-mail(s) |
[email protected]
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Phone |
+81-3-5841-1427
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Organization name |
The University of Tokyo
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Department |
Center for Disease Biology and Integrative Medicine
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Lab |
Clinical Biotechnology
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Street address |
7-3-1 Hongo
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City |
Bunkyo-ku |
State/province |
Tokyo |
ZIP/Postal code |
113-8655 |
Country |
Japan |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (6)
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This SubSeries is part of SuperSeries: |
GSE76187 |
Sp7/Osterix is restricted to bone-forming vertebrates where it acts as a Dlx co-factor in osteoblast specification |
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Relations |
BioProject |
PRJNA306574 |
SRA |
SRP067609 |