ZFIN ID: ZDB-PUB-110713-69
Knock-down of cathepsin D affects the retinal pigment epithelium, impairs swim-bladder ontogenesis and causes premature death in zebrafish
Follo, C., Ozzano, M., Mugoni, V., Castino, R., Santoro, M., and Isidoro, C.
Date: 2011
Source: PLoS One   6(7): e21908 (Journal)
Registered Authors: Mugoni, Vera, Santoro, Massimo
Keywords: none
MeSH Terms:
  • Air Sacs/embryology
  • Air Sacs/enzymology*
  • Air Sacs/growth & development
  • Animals
  • Base Sequence
  • Body Size/genetics
  • Cathepsin D/deficiency*
  • Cathepsin D/genetics*
  • Embryonic Development/genetics
  • Gene Knockdown Techniques*
  • Humans
  • Longevity/genetics
  • Mutation
  • Oligonucleotides/genetics
  • Phenotype
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Retinal Pigment Epithelium/embryology
  • Retinal Pigment Epithelium/enzymology*
  • Retinal Pigment Epithelium/growth & development
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish/growth & development
  • Zebrafish/physiology*
  • Zygote/metabolism
PubMed: 21747967 Full text @ PLoS One
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ABSTRACT
The lysosomal aspartic protease Cathepsin D (CD) is ubiquitously expressed in eukaryotic organisms. CD activity is essential to accomplish the acid-dependent extensive or partial proteolysis of protein substrates within endosomal and lysosomal compartments therein delivered via endocytosis, phagocytosis or autophagocytosis. CD may also act at physiological pH on small-size substrates in the cytosol and in the extracellular milieu. Mouse and fruit fly CD knock-out models have highlighted the multi-pathophysiological roles of CD in tissue homeostasis and organ development. Here we report the first phenotypic description of the lack of CD expression during zebrafish (Danio rerio) development obtained by morpholino-mediated knock-down of CD mRNA. Since the un-fertilized eggs were shown to be supplied with maternal CD mRNA, only a morpholino targeting a sequence containing the starting ATG codon was effective. The main phenotypic alterations produced by CD knock-down in zebrafish were: 1. abnormal development of the eye and of retinal pigment epithelium; 2. absence of the swim-bladder; 3. skin hyper-pigmentation; 4. reduced growth and premature death. Rescue experiments confirmed the involvement of CD in the developmental processes leading to these phenotypic alterations. Our findings add to the list of CD functions in organ development and patho-physiology in vertebrates.
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