Expression and Functional Analysis of a Novel Isoform of Gicerin, an Immunoglobulin Superfamily Cell Adhesion Molecule (*)

  1. Eiichi Taira§,
  2. Tomoko Nagino,
  3. Hideo Taniura,
  4. Natsuki Takaha,
  5. Cheol-Hee Kim,
  6. Che-Hui Kuo,
  7. Bing-Shen Li,
  8. Hiroshi Higuchi and
  9. Naomasa Miki
  1. From the Department of Pharmacology 1, Osaka University Medical School, 2-2 Yamadaoka, Suita, Osaka 565, Japan
  1. § To whom correspondence should be addressed:
    Dept. of Pharmacology 1, Osaka Universit Medical School, 2-2 Yamadaoka, Suita, Osaka 565, Japan.
    Tel.: 81-6-879-3521; Fax: 81-6-879-3529.

Abstract

We have cloned a novel cDNA of gicerin, a cell adhesion molecule belonging to the immunoglobulin superfamily. Both gicerin isoforms share the same extracellular domain, which has five immunoglobulin-like loop structures and a transmembrane domain as s-gicerin, but differ in the cytoplasmic tail domain. As the newly identified form has a larger cytoplasmic domain than the previously reported form, we refer to them as l-gicerin and s-gicerin, respectively. l-gicerin is transcribed from a distinct mRNA containing an inserted sequence not found in s-gicerin mRNA which caused a frameshift for the coding region for a cytoplasmic domain. Previous studies demonstrated that gicerin showed a doublet band of 82 and 90 kDa in chicken gizzard smooth muscle. We report that the 82-kDa protein corresponds to s-gicerin and the 90-kDa protein to l-gicerin. We also found that the two gicerin isoforms are expressed differentially in the developing nervous system. Functional analysis of these gicerin isoforms in stable transfectants revealed that they had differ in their homophilic adhesion properties, as well as in heterophilic cell adhesion assayed with neurite outgrowth factor. In addition, these isoforms have neurite-promoting activity by their homophilic adhesion, but differ in their ability to promote neurite outgrowth.

Footnotes

  • (*) This work was supported by a grant-in-aid for Scientific Research from the Ministry of Education, Science, and Culture of Japan. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore by hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    The nucleotide sequence(s) reported in this paper has been submitted to the GenBank(TM)/EMBL Data Bank with accession number(s) D49849 [GenBank](l-gicerin).

  • 1 The abbreviations used are:

    MAG

    myelin-associated glycoprotein

    NOF

    neurite outgrowth factor

    RT-PCR

    reverse transcription polymerase chain reaction

    PAGE

    polyacrylamide gel electrophoresis

    FCS

    fetal calf serum

    CG

    ciliary ganglion

    bp

    base pair(s)

    NCAM

    neural cell adhesion molecule.

    • Received July 17, 1995.
    • Revision received September 21, 1995.
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