ZFIN ID: ZDB-PUB-191223-17
Combinatorial action of NF-Y and TALE at embryonic enhancers defines distinct gene expression programs during zygotic genome activation in zebrafish
Stanney, W., Ladam, F., Donaldson, I.J., Parsons, T.J., Maehr, R., Bobola, N., Sagerström, C.G.
Date: 2019
Source: Developmental Biology   459(2): 161-180 (Journal)
Registered Authors: Sagerström, Charles
Keywords: Embryogenesis, Enhancer, Maternal, Nucleosome, Transcription, Zygotic
MeSH Terms:
  • Animals
  • CCAAT-Binding Factor/metabolism*
  • Cilia/genetics
  • Embryonic Development/genetics
  • Female
  • Gene Expression*
  • Gene Expression Regulation, Developmental
  • Genome*
  • Homeodomain Proteins/genetics
  • Homeodomain Proteins/metabolism*
  • Male
  • Transcriptional Activation*
  • Zebrafish/embryology*
  • Zebrafish Proteins
  • Zygote/metabolism*
PubMed: 31862379 Full text @ Dev. Biol.
Animal embryogenesis is initiated by maternal factors, but zygotic genome activation (ZGA) shifts regulatory control to the embryo during blastula stages. ZGA is thought to be mediated by maternally provided transcription factors (TFs), but few such TFs have been identified in vertebrates. Here we report that NF-Y and TALE TFs bind zebrafish genomic elements associated with developmental control genes already at ZGA. In particular, co-regulation by NF-Y and TALE is associated with broadly acting genes involved in transcriptional control, while regulation by either NF-Y or TALE defines genes in specific developmental processes, such that NF-Y controls a cilia gene expression program while TALE controls expression of hox genes. We also demonstrate that NF-Y and TALE-occupied genomic elements function as enhancers during embryogenesis. We conclude that combinatorial use of NF-Y and TALE at developmental enhancers permits the establishment of distinct gene expression programs at zebrafish ZGA.