| First Author | Kohlhase J | Year | 2000 |
| Journal | Mamm Genome | Volume | 11 |
| Issue | 1 | Pages | 64-8 |
| PubMed ID | 10602995 | Mgi Jnum | J:59254 |
| Mgi Id | MGI:1351248 | Doi | 10.1007/s003350010012 |
| Citation | Kohlhase J, et al. (2000) Genomic cloning, chromosomal mapping, and expression analysis of msal-2. Mamm Genome 11(1):64-8 |
| abstractText | Mutations of SALL1 related to spalt of Drosophila have been found to cause Townes-Brocks syndrome, suggesting a function of SALL1 for the development of anus, limbs, ears, and kidneys. No function is yet known for SALL2, another human spalt-like gene. The structure of SALL2 is different from SALL1 and all other vertebrate spalt-like genes described in mouse, Xenopus, and Medaka, suggesting that SALL2-like genes might also exist in other vertebrates. Consistent with this hypothesis, we isolated and characterized a SALL2 homologous mouse gene, Msal-2. In contrast to other vertebrate spalt-like genes both SALL2 and Msal-2 encode only three double zinc finger domains, the most carboxyterminal of which only distantly resembles spalt-like zinc fingers. The evolutionary conservation of SALL2/Msal-2 suggests that two lines of sal-like genes with presumably different functions arose from an early evolutionary duplication of a common ancestor gene. Msal-2 is expressed throughout embryonic development but also in adult tissues, predominantly in brain. However, the function of SALL2/Msal-2 still needs to be determined. |
