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Status |
Public on Dec 29, 2021 |
Title |
Loss of ATF4 leads to functional aging-like attrition of adult hematopoietic stem cells [RNA-seq] |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
We collected significant amount of phenotypic and mechanistic data from a ATF4 knockout mouse model and demonstrated that HSC defects with an aging-like phenotype (expanded pool of phenotypical HSCs, decreased number of functional HSCs, impaired repopulating and self-renewal capacities of HSCs and myeloid bias) occurred in the ATF4 KO mice, suggesting that not only ATF4 indeed represents a pivotal factor for adult HSC function but also we had successfully constructed an ideal and attractive model to study aging and aging-related disease.
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Overall design |
This dataset contains RNA-seq experiments of long-term HSCs isolated from ATF4WT or ATF4 CKO mice.
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Contributor(s) |
Sun Y, Li M |
Citation(s) |
34936448 |
Submission date |
Jun 13, 2019 |
Last update date |
Dec 29, 2021 |
Contact name |
Yan Sun |
E-mail(s) |
suny69@mail.sysu.edu.cn
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Organization name |
Sun Yat-sen University
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Street address |
Zhong shan 2nd Road, Building 74
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City |
Guangzhou |
State/province |
Guangdong |
ZIP/Postal code |
510080 |
Country |
China |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (4)
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This SubSeries is part of SuperSeries: |
GSE132683 |
Loss of ATF4 leads to functional aging-like attrition of adult hematopoietic stem cells |
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Relations |
BioProject |
PRJNA548749 |
SRA |
SRP201328 |