4.7 Article

cDNA cloning of the immunoglobulin heavy chain genes in banded houndshark Triakis scyllium

Journal

FISH & SHELLFISH IMMUNOLOGY
Volume 29, Issue 5, Pages 854-861

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fsi.2010.07.034

Keywords

Banded houndshark; Immunoglobulin heavy chain; IgM; IgNAR; IgW

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan [21248025]
  2. Grants-in-Aid for Scientific Research [21248025] Funding Source: KAKEN

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In this study, cDNAs encoding the secreted forms of the immunoglobulin (Ig) heavy chains of IgM, IgNAR, and IgW were cloned from the banded houndshark Triakis scyllium. Two clones for the IgM heavy chains encoded 569 and 570 amino acids, whose conserved (C) region showed 47-70% amino acid identities to those reported in other cartilaginous fish. Four clones for the IgNAR encoded 673-670 amino acids with conserved Ig-superfamily domains. The IgNAR C region showed 56-69% amino acid identities to those so far reported. High-throughput sequencing revealed that in most of the IgNAR sequences, the two variable regions (CDR1 and CDR3) each possess a cysteine residue. Three types of IgW were identified; one contained Ig-superfamily domains that are in other cartilaginous fish, one lacks the 3rd domain in the constant region, and one lacks the 3rd to 5th domains. Despite these differences, the IgW isoforms clustered with IgWs of other cartilaginous fishes and the C regions showed 47-89% amino acid identities. mRNAs for IgM and IgNAR were detected in various tissues, while IgW mRNA was mainly detected in pancreas. The banded hounded shark also has IgM, IgW and IgNAR as well as the other cartilaginous fish with unique IgW isoform. (C) 2010 Elsevier Ltd. All rights reserved.

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