| First Author | Kohama K | Year | 2005 |
| Journal | Neurochem Int | Volume | 46 |
| Issue | 6 | Pages | 465-70 |
| PubMed ID | 15769548 | Mgi Jnum | J:99601 |
| Mgi Id | MGI:3583062 | Doi | 10.1016/j.neuint.2004.12.006 |
| Citation | Kohama K, et al. (2005) Molecular cloning and analysis of the mouse gicerin gene. Neurochem Int 46(6):465-70 |
| abstractText | Gicerin is a cell adhesion molecule, which has five immunoglobulin-like loop structures in an extracellular domain followed by a single transmembrane domain and a short cytoplasmic tail. We have reported that gicerin participates in neurite extension and structural organization of the nervous system, and its expression in the nervous system is high during the development and dramatically decreased after birth. To elucidate the mechanism how the expression of gicerin is regulated, we performed a genomic cloning of a mouse gicerin. A fragment of 16 kbp genomic clone contained 8 kbp gicerin gene composed of 16 exons with 6 kbp upstream region. Genomic cloning revealed that two isoforms of gicerin were generated by an alternative splicing of exon 15 results in cytoplasmic domains composed of either 63 or 21 amino acids. As for an expressional regulation of gicerin, we found that the mRNA content of gicerin in PC12 cells was regulated by cAMP. Quantitative-PCR analysis revealed that forskolin induced four-fold increase of gicerin mRNA. To characterize the involvement of its promoter region, we examined the promoter activity in PC12 cells by a luciferase-reporter assay. We found that a CRE site located at 60 bp upstream of gicerin gene was responsible for the increase of its mRNA induced by forskolin. |
