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Status |
Public on May 26, 2021 |
Title |
Terminal uridyltransferase 7 regulates TLR4-triggered inflammation by controlling Regnase-1 mRNA uridylation and degradation |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
We revealed that the transcriptome of the mammalian cells under inflammatory status using RNA Sequencing (RNA-Seq). The transcriptome of BMDMs from wild-type and Tut7-/- was compared to baseline. The fold-change was presented by the logarithm of p-values to the base 2 and the significance was presented by the negative logarithm of that to the base 10. log2FC > +0.2 and log2FC < -0.2 indicate the increase of transcript levels by >20% and decreased by >20%, respectively. Among the 352 genes, 111 of them involving in innate immune response were downregulated in Tut7-/- cells.
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Overall design |
LPS-induced BMDMs mRNA profiles of 7-week-old wild type and Tut7-/- mice were generated by deep sequencing, in duplicate, using Illumina HiSeq PE150
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Contributor(s) |
Lin C |
Citation(s) |
34188032 |
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Submission date |
Aug 21, 2019 |
Last update date |
Jul 27, 2021 |
Contact name |
Li-Chung Hsu |
E-mail(s) |
lichunghsu@ntu.edu.tw
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Phone |
+886-2-23123456
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Organization name |
National Taiwan University
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Department |
Graduate institute of Molecular Medicine
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Street address |
No.7, ChungShan S. Rd., ZhongZheng Dist.
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City |
Taipei |
ZIP/Postal code |
10002 |
Country |
Taiwan |
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Platforms (1) |
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Samples (8)
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Relations |
BioProject |
PRJNA561406 |
SRA |
SRP219042 |