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Series GSE163483 Query DataSets for GSE163483
Status Public on Jun 09, 2021
Title Transcriptionally regulated energy metabolism drives early erythropoiesis (RRBS)
Organism Danio rerio
Experiment type Methylation profiling by high throughput sequencing
Summary Transcription and metabolism both influence cell function yet dedicated transcriptional control of metabolic pathways that regulate cell fate has rarely been defined. Through a chemical suppressor screen, we discovered that inhibition of the pyrimidine biosynthesis enzyme DHODH rescues erythroid differentiation in bloodless moonshine mutant embryos defective for the transcription elongation factor tif1γ. This rescue depends on the functional link of DHODH to mitochondrial respiration. TIF1γ directly controls coenzyme Q synthesis gene expression. Upon tif1γ loss, coenzyme Q levels are reduced, and a high succinate/α-ketoglutarate ratio leads to increased histone methylation. A coenzyme Q analogue rescues moonshine’s bloodless phenotype. These results demonstrate mitochondrial metabolism is a key output of a lineage transcription factor that drives cell fate decisions in the early blood lineage.
 
Overall design tif1γ (ENSDART00000020116.9/NM_001002871.2) was knocked down (tif1γ KD) by injecting 1 ng of an ATG-blocking morpholino (Gene Tools, 5’→3’ morpholino sequence ATCTTGGCCTTTGTTGTCCGCCATC) into zebrafish wild-type (TU) embryos at the 1-2 cell stage. As a control (Ctrl KD), 1 ng of a Standard Control oligo (designed by Gene Tools, 5’→3’ morpholino sequence CCTCTTACCTCAGTTACAATTTATA) was injected into zebrafish embryos at the 1-2 cell stage. tif1γ KD and Ctrl KD embryos from each clutch were harvested at 11 hpf, 22 hpf and 48 hpf by snap-freezing them, followed by extraction of genomic DNA and processing for reduced representation bisulfite sequencing (RRBS).
 
Contributor(s) Rossmann MP, Hetzel S, Weigert R, Yang S, Meissner A, Zon LI
Citation(s) 33986176
Submission date Dec 18, 2020
Last update date Jun 09, 2021
Contact name Leonard Zon
E-mail(s) zon@enders.tch.harvard.edu
Organization name Boston Children's Hospital
Department Oncology/Hematology
Street address 1 Blackfan Circle
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL24995 Illumina NovaSeq 6000 (Danio rerio)
Samples (12)
GSM4979862 RRBS_somites_control_KD_clutch8
GSM4979863 RRBS_somites_control_KD_clutch9
GSM4979864 RRBS_somites_tif1g_KD_clutch8
This SubSeries is part of SuperSeries:
GSE136456 Transcriptionally regulated energy metabolism drives early erythropoiesis
Relations
BioProject PRJNA686370
SRA SRP298452

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE163483_RAW.tar 171.0 Mb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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