| First Author | Alpy F | Year | 2005 |
| Journal | Genesis | Volume | 43 |
| Issue | 2 | Pages | 59-70 |
| PubMed ID | 16100707 | Mgi Jnum | J:102740 |
| Mgi Id | MGI:3608022 | Doi | 10.1002/gene.20154 |
| Citation | Alpy F, et al. (2005) Generation of a conditionally null allele of the laminin alpha1 gene. Genesis 43(2):59-70 |
| abstractText | Laminins are heterotrimeric glycoproteins of the basement membranes. Laminin 1 (alpha1, beta1, gamma1) is the major laminin expressed during early mouse embryogenesis. To gain access to the physiological function of laminin alpha1 chain, we developed a conditionally null allele of its encoding gene (Lama1) using the cre/loxP system. Floxed-allele-carrying mice (Lama1(flox/flox)) display no overt phenotype. Lama1(flox/flox) mice were crossed with transgenic deleter mice (CMV-Cre) to generate Lama1-deficient mice (Lama1(Delta/Delta)). Lama1(Delta/Delta) embryos die during the early postimplantation period after embryonic day 6.5. They lack Reichert's membrane, an extraembryonic basement membrane in which laminin alpha1 is normally highly expressed. In parallel, Lama1(Delta/Delta) embryos display 1) parietal and visceral endoderm differentiation defects with altered expression of cytokeratin 19 and GATA4, respectively, and 2) an induction of apoptosis. This new mouse model is of particular interest as it will allow time- and tissue-specific inactivation of the Lama1 gene in various organs. |
