| First Author | Pimenta AF | Year | 2004 |
| Journal | Genomics | Volume | 83 |
| Issue | 5 | Pages | 790-801 |
| PubMed ID | 15081109 | Mgi Jnum | J:134450 |
| Mgi Id | MGI:3785854 | Doi | 10.1016/j.ygeno.2003.11.013 |
| Citation | Pimenta AF, et al. (2004) Characterization of the genomic structure of the mouse limbic system-associated membrane protein (Lsamp) gene. Genomics 83(5):790-801 |
| abstractText | The Lsamp gene encodes the limbic system-associated membrane protein (LAMP) an immunoglobulin (Ig) superfamily member with three Ig domains and a glycosylphosphatidylinositol anchor. LAMP is expressed by neurons composing the limbic system, is highly conserved between rodents and human, and has structural and functional properties that substantiate its role in the formation of limbic circuits. We report here the genomic organization of the Lsamp gene. The Lsamp gene is composed of 11 exons distributed over 2.2 megabases (Mb). Two exons 1 are separated by approximately 1.6 Mb and contribute to the unusual large size of the gene. Alternative spliced Lsamp mRNAs are generated from distinct promoter regions associated with the two exons 1 that encode distinct signal peptides and thus generate identical native mature polypetides. Additional diversity is created by the use of two small exons to include an insertion of 23 amino acids within the polypeptide C-terminal region of the mature protein. The genomic features of the Lsamp gene described here indicate an intricate mechanism of gene expression regulation that may be relevant in the context of human neuropsychiatric and neurological disorders, where LAMP expression may be altered. |
