PUBLICATION

Protein Arginine Methyltransferase 6 (Prmt6) Is Essential for Early Zebrafish Development through the Direct Suppression of gadd45αa Stress Sensor Gene

Authors
Zhao, X.X., Zhang, Y.B., Ni, P.L., Wu, Z.L., Yan, Y.C., Li, Y.P.
ID
ZDB-PUB-151022-1
Date
2016
Source
The Journal of biological chemistry   291(1): 402-12 (Journal)
Registered Authors
Keywords
apoptosis, c-Jun N-terminal kinase (JNK), gadd45αa, histone methylation, p38, prmt6, zebrafish
Datasets
GEO:GSE63735
MeSH Terms
  • Animals
  • Apoptosis/drug effects
  • Cell Cycle Proteins/genetics*
  • Cell Cycle Proteins/metabolism
  • Embryonic Development*/drug effects
  • Embryonic Development*/genetics
  • JNK Mitogen-Activated Protein Kinases/metabolism
  • Morpholinos/pharmacology
  • Nuclear Proteins/genetics*
  • Nuclear Proteins/metabolism
  • Protein-Arginine N-Methyltransferases/genetics*
  • Protein-Arginine N-Methyltransferases/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Stress, Physiological/drug effects
  • Stress, Physiological/genetics
  • Up-Regulation/drug effects
  • Zebrafish/embryology*
  • Zebrafish/genetics*
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism
  • p38 Mitogen-Activated Protein Kinases/metabolism
PubMed
26487724 Full text @ J. Biol. Chem.
Abstract
Histone lysine methylation is important in early zebrafish development; however, the role of histone arginine methylation in this process remains unclear. H3R2me2a, generated by protein arginine methyltransferase 6 (Prmt6), is a repressive mark. To explore the role of Prmt6 and H3R2me2a during zebrafish embryogenesis, we identified the maternal characteristic of prmt6, and designed two prmt6-specific morpholino-oligos (MOs) to study its importance in early development, application of which led to early epiboly defects, and significantly reduced the level of H3R2me2a marks. Prmt6 mRNA could rescue the epiboly defects and the H3R2me2a reduction in the prmt6 morphants. Functionally, microarray data demonstrated that growth arrest and DNA-damage-inducible, alpha, a (gadd45αa) was a significantly upregulated gene in MO treated embryos, the activity of which was linked to the activation of the p38/JNK pathway and apoptosis. Importantly, gadd45αa MO and p38/JNK inhibitors could partially rescue the defect of prmt6 morphants, the downstream-targets of Prmt6 and the apoptosis ratios of the prmt6 morphants. Moreover, the results of ChIP quantitative real-time PCR and Luciferase Reporter Assay indicated that gadd45αa is a repressive target of Prmt6. Taken together, these results suggest that maternal Prmt6 is essential to early zebrafish development by directly repressing gadd45αa.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping