PUBLICATION

The basal function of teleost prolactin as a key regulator on ion uptake identified with zebrafish knockout models

Authors
Shu, Y., Lou, Q., Dai, Z., Dai, X., He, J., Hu, W., Yin, Z.
ID
ZDB-PUB-160105-3
Date
2016
Source
Scientific Reports   6: 18597 (Journal)
Registered Authors
He, Jiangyan, Hu, Wei, Yin, Zhan
Keywords
Animal physiology, Developmental biology, Molecular evolution, Pituitary gland
MeSH Terms
  • Animals
  • Anion Transport Proteins/metabolism
  • Base Sequence
  • Female
  • Gene Knockout Techniques
  • Gills/cytology
  • Gills/metabolism
  • Ion Transport
  • Male
  • Osmoregulation
  • Prolactin/genetics*
  • Prolactin/metabolism
  • Sodium/metabolism
  • Zebrafish
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism
PubMed
26726070 Full text @ Sci. Rep.
Abstract
Prolactin (PRL) is an anterior pituitary hormone with a broad range of functions. Its ability to stimulate lactogenesis, maternal behavior, growth and development, osmoregulation, and epithelial ion transport has been reported in many vertebrates. In our present study, we have targeted the zebrafish prl locus via transcription activator-like effector nucleases (TALENs). Two independent targeted mutant lines with premature termination of the putative sequence of PRL peptides were generated. All prl-deficient zebrafish progeny died at 6-16 days post-fertilization stage (dpf) in egg water. However, the prl-deficient larvae thrived and survived through adulthood in brackish water (5175 mg/L ocean salts), without obvious defects in somatic growth or reproduction. When raised in egg water, the expression levels of certain key Na(+)/Cl(-) cotransporters in the gills and Na(+)/K(+)-ATPase subunits, Na(+)/H(+) exchangers and Na(+)/Cl(-) transporters in the pronephros of prl-deficient larvae were down-regulated at 5 dpf, which caused Na(+)/K(+)/Cl(-) uptake defects in the mutant fish at 6 dpf. Our present results demonstrate that the primary function of zebrafish prl is osmoregulation via governing the uptake and homeostasis of Na(+), K(+) and Cl(-). Our study provides valuable evidence to understand the mechanisms of PRL function better through both phylogenetic and physiological perspectives.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping