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Cell-specific transcriptional control of mitochondrial metabolism by TIF1γ drives erythropoiesis.

Marlies P RossmannKaren HoiVictoria ChanBrian J AbrahamSong YangJames P MullahooMalvina PapanastasiouYing WangIlaria EliaJulie R PerlinElliott J HagedornSara HetzelRaha WeigertSejal VyasPartha P NagLucas B SullivanCurtis R WarrenBilguujin DorjsurenEugenia Custo GreigIsaac AdattoChad A CowanStuart L SchreiberRichard A YoungAlexander MeissnerMarcia C HaigisSiegfried HekimiSteven A CarrLeonard I Zon
Published in: Science (New York, N.Y.) (2021)
Transcription and metabolism both influence cell function, but dedicated transcriptional control of metabolic pathways that regulate cell fate has rarely been defined. We discovered, using a chemical suppressor screen, that inhibition of the pyrimidine biosynthesis enzyme dihydroorotate dehydrogenase (DHODH) rescues erythroid differentiation in bloodless zebrafish moonshine (mon) mutant embryos defective for transcriptional intermediary factor 1 gamma (tif1γ). This rescue depends on the functional link of DHODH to mitochondrial respiration. The transcription elongation factor TIF1γ directly controls coenzyme Q (CoQ) synthesis gene expression. Upon tif1γ loss, CoQ levels are reduced, and a high succinate/α-ketoglutarate ratio leads to increased histone methylation. A CoQ analog rescues mon's bloodless phenotype. These results demonstrate that mitochondrial metabolism is a key output of a lineage transcription factor that drives cell fate decisions in the early blood lineage.
Keyphrases
  • cell fate
  • transcription factor
  • gene expression
  • dna methylation
  • oxidative stress
  • dna binding
  • single cell
  • mouse model
  • genome wide
  • cell therapy
  • high throughput
  • genome wide identification