PUBLICATION

A complement factor B-like cDNA clone from the zebrafish (Brachydanio rerio)

Authors
Seeger, A., Mayer, W.E., and Klein, J.
ID
ZDB-PUB-970326-9
Date
1996
Source
Molecular immunology   33(6): 511-520 (Journal)
Registered Authors
Klein, Jan, Mayer, Werner E.
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Complement C2/genetics
  • Complement Factor B/genetics*
  • DNA Primers/chemistry
  • DNA, Complementary/genetics
  • Gene Library
  • Humans
  • Molecular Sequence Data
  • Phylogeny
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Zebrafish/genetics*
PubMed
8700167 Full text @ Mol. Immunol.
Abstract
An important molecule in the activation of the complement system in vertebrates is factor B, a serine protease with a molecular mass of 95,000. Factor B and the complement component C2 are thought to have arisen by gene duplication. In mammals and in Xenopus the factor B gene is linked to the major histocompatibility complex (MHC), whereas in domestic fowl it segregates independently of the MHC. Here we describe the isolation of a cDNA clone coding for factor B in the zebrafish, Brachydanio rerio. The deduced protein sequence exhibits a characteristic mosaic structure consisting of the short consensus repeat (SCR), the von Willebrand factor, and the serine protease domains. The estimated time of factor B and C2 divergence (approximately 350 million years ago), combined with the fact that C2 has thus far been found only in mammals, suggest that the factor B-C2 gene duplication occurred after the divergence of mammal-like reptiles from other reptiles and hence also birds. After the duplication, the C2 component evolved significantly faster than factor B.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping