PUBLICATION

Characterization of F-spondin in Japanese flounder (Paralichthys olivaceus) and its role in the nervous system development of teleosts

Authors
Hu, H., Xin, N., Liu, J., Liu, M., Wang, Z., Wang, W., Zhang, Q., Qi, J.
ID
ZDB-PUB-150924-14
Date
2016
Source
Gene   575(2 Pt 3): 623-31 (Journal)
Registered Authors
Keywords
F-spondin, Japanese flounder, Nervous system development, Zebrafish
MeSH Terms
  • Animals
  • Cloning, Molecular
  • Extracellular Matrix Proteins/genetics*
  • Extracellular Matrix Proteins/metabolism*
  • Fish Proteins/genetics
  • Fish Proteins/metabolism
  • Flounder/anatomy & histology*
  • Flounder/embryology
  • Flounder/metabolism
  • Gene Expression Regulation, Developmental
  • Gonads/metabolism
  • Nervous System/growth & development*
  • Nervous System/metabolism
  • Organ Specificity
  • Phylogeny
PubMed
26390814 Full text @ Gene
Abstract
F-spondin was originally isolated from the developing embryonic floor plate of vertebrates, secreting numerous kinds of neuron-related molecules. The protein performs a positive function in nervous system development, which is attributed to the high conservation of F-spondin protein, an extracellular matrix (ECM) protein in several species. However, its precise function remains unknown, especially in marine fish. In this study, the F-spondin of Japanese flounder (Paralichthys olivaceus). was cloned, and its expression pattern and structural characteristics were analyzed. The 2421bp-long cDNA ORF of PoF-spondin was obtained and divided into 14 exons spread over 61,496bp of the genomic sequence. Phylogenetic analysis showed that PoF-spondin was actually the ortholog of the human spon1 gene and shared high identities with other teleost spon1a genes. Quantitative RT-PCR analysis showed that PoF-spondin was maternally expressed, and transcripts were present from one-cell stage to hatching stage, peaking at tailbud stage. Tissue distribution analysis indicated that PoF-spondin was detectable mainly in the gonads (especially in the ovary) and the brain. Whole mount in situ hybridization analysis revealed that the PoF-spondin transcription distributed throughout the cleavage of the ball in the early stage and expressed at a high level in the floor plate of the trunk at tailbud and pre-hatching stages. Furthermore, the expression of genes related to nervous system development (spon1b, foxo3b, and foxj1a) was significantly increased after the injection of PoF-spondin into the embryos of wild-type zebrafish. Furthermore, PoF-spondin significantly suppressed the expression of the chordamesoderm marker gene ntl, increased the expression of otx2/krox20, ectoderm mark genes, and left the expression of dorsal mesodermal marker gene gsc unaffected at 50% epiboly stage in zebrafish. In short, our results suggest that PoF-spondin functions in the development of the teleost nervous system.
Genes / Markers
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping