OVERLAPPING AND DIFFERENTIAL EXPRESSION OF BIG-2, BIG-1, TAG-1, AND F3 - 4 MEMBERS OF AN AXON-ASSOCIATED CELL-ADHESION MOLECULE SUBGROUP OFTHE IMMUNOGLOBULIN SUPERFAMILY

Citation
Y. Yoshihara et al., OVERLAPPING AND DIFFERENTIAL EXPRESSION OF BIG-2, BIG-1, TAG-1, AND F3 - 4 MEMBERS OF AN AXON-ASSOCIATED CELL-ADHESION MOLECULE SUBGROUP OFTHE IMMUNOGLOBULIN SUPERFAMILY, Journal of neurobiology, 28(1), 1995, pp. 51-69
Citations number
55
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
00223034
Volume
28
Issue
1
Year of publication
1995
Pages
51 - 69
Database
ISI
SICI code
0022-3034(1995)28:1<51:OADEOB>2.0.ZU;2-4
Abstract
Axon-associated cell adhesion molecules (AxCAMs) play crucial roles in the formation, maintenance, and plasticity of functional neuronal net works. We report here a molecular cloning of a novel AxCAM, BIG-2. BIG -2 is a member of TAG-1/F3 subgroup of the immunoglobulin (Ig) superfa mily, with six Ig-like domains, four fibronectin type III-like repeats , and a glycosyl phosphatidylinositol-anchoring domain. Recombinant BI G-2 protein had a neurite outgrowth-promoting activity when used as a substrate for neurons in vitro. To survey the spatial expression patte rn of BIG-2 in comparison with other TAG-1/F3 subgroup members, an in situ hybridization analysis was performed in adult and developing rat brain sections with riboprobes specific for BIG-2, BIG-1, TAG-1, and F 3. The four AxCAM transcripts displayed cell type-specific expression patterns with overlapping and distinct profiles. In adult hippocampus, for example, we observed BIG-1 mRNA specifically in granule cells of the dentate gyrus, BIG-2 mRNA highly in the CA1 pyramidal cells, TAG-1 mRNA predominantly in the CA3 pyramidal cells, and F3 mRNA in neurons in all of these fields. These results suggest that BIG-2, BIG-1, TAG- 1, and F3 may play important roles in the formation and maintenance of specific neuronal networks in the brain. (C) 1995 John Wiley & Sons, Inc.