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ZFIN ID: ZDB-PUB-070210-2
Analysis of the exon-intron structures of fish, amphibian, bird and mammalian hatching enzyme genes, with special reference to the intron loss evolution of hatching enzyme genes in Teleostei
Kawaguchi, M., Yasumasu, S., Hiroi, J., Naruse, K., Suzuki, T., and Iuchi, I.
Date: 2007
Source: Gene   392(1-2): 77-88 (Journal)
Registered Authors: Naruse, Kiyoshi
Keywords: Takifugu rubripes, Tetraodon nigroviridis, Hatching enzyme, Astacin family metallo-protease, Intron loss evolution, Teleost fish
MeSH Terms:
  • Amino Acid Sequence
  • Amphibians/genetics*
  • Animals
  • Base Sequence
  • Birds/genetics*
  • Cloning, Molecular
  • Embryo, Nonmammalian
  • Evolution, Molecular
  • Exons*
  • Fishes/genetics*
  • Gene Deletion
  • Humans
  • Introns*
  • Mammals/genetics*
  • Metalloendopeptidases/genetics*
  • Molecular Sequence Data
  • Phylogeny
  • Sequence Homology, Amino Acid
  • Takifugu/genetics
PubMed: 17222522 Full text @ Gene
Using gene cloning and in silico cloning, we analyzed the structures of hatching enzyme gene orthologs of vertebrates. Comparison led to a hypothesis that hatching enzyme genes of Japanese eel conserve an ancestral structure of the genes of fishes, amphibians, birds and mammals. However, the exon-intron structure of the genes was different from species to species in Teleostei: Japanese eel hatching enzyme genes were 9-exon-8-intron genes, and zebrafish genes were 5-exon-4-intron genes. In the present study, we further analyzed the gene structures of fishes belonging to Acanthopterygii. In the species of Teleostei we examined, diversification of hatching enzyme gene into two paralogous genes for HCE (high choriolytic enzyme) and LCE (low choriolytic enzyme) was found only in the acanthopterygian fishes such as medaka Oryzias latipes, Fundulus heteroclitus, Takifugu rubripes and Tetraodon nigroviridis. In addition, the HCE gene had no intron, while the LCE gene consisted of 8 exons and 7 introns. Phylogenetic analysis revealed that HCE and LCE genes were paralogous to each other, and diverged during the evolutionary lineage to Acanthopterygii. Analysis of gene synteny and cluster structure showed that the syntenic genes around the HCE and LCE genes were highly conserved between medaka and Teraodon, but such synteny was not found around the zebrafish hatching enzyme genes. We hypothesize that the zebrafish hatching enzyme genes were translocated from chromosome to chromosome, and lost some of their introns during evolution.