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Status |
Public on Dec 29, 2014 |
Title |
LincRNA-p21 Blocks Somatic Cell Reprogramming by Sustaining H3K9me3 and CpG Methylation at Pluripotent Gene Promoters |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Through expression profiling and functional screening we have identified the large intergenic non-coding RNA p21 (lincRNA-p21) as a barrier for reprogramming. LincRNA-p21 is induced by p53 but contrary to its role in the DNA damage response it does not promote apoptosis or cell senescence in reprogramming. Instead, lincRNA-p21 associates with the H3K9 methyltransferase Setdb1 and the maintenance DNA methyltransferase Dnmt1 in separate complexes that are facilitated by the RNA binding protein hnRNP-K.
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Overall design |
RNA-seq expression data during MEF to iPSC reprogramming using three shRNAs, targetting either luciferase (control), lincRNA-p21 and hnRNP-K. Days 6, 9 and 12 of the reprogramming timecourse were analyzed
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Contributor(s) |
Hutchins AP, Bao X, Esteban MA |
Citation(s) |
25512341 |
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Submission date |
May 27, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Andrew P Hutchins |
E-mail(s) |
andrewh@sustech.edu.cn
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Organization name |
Southern University of Science and Technology
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Department |
Bioinformatics
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Lab |
Bioinformatics and Genomics
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Street address |
1088 Xueyuan Rd
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City |
Shenzhen |
ZIP/Postal code |
518055 |
Country |
China |
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Platforms (1) |
GPL13112 |
Illumina HiSeq 2000 (Mus musculus) |
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Samples (9)
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Relations |
BioProject |
PRJNA248614 |
SRA |
SRP042278 |