| First Author | Bernards A | Year | 1993 |
| Journal | Hum Mol Genet | Volume | 2 |
| Issue | 6 | Pages | 645-50 |
| PubMed ID | 8353485 | Mgi Jnum | J:12590 |
| Mgi Id | MGI:60831 | Doi | 10.1093/hmg/2.6.645 |
| Citation | Bernards A, et al. (1993) Mouse neurofibromatosis type 1 cDNA sequence reveals high degree of conservation of both coding and non-coding mRNA segments. Hum Mol Genet 2(6):645-50 |
| abstractText | To identify evolutionary conserved domains and facilitate the recognition of potentially significant mutations in NF1 patients or tumors, we have determined the complete approximately 12 kb sequence of mouse neurofibromatosis type 1 mRNA. The sequence predicts a 2841 amino acid protein that is more than 98% identical to human neurofibromin. All but 9 of the 45 amino acid differences between mouse and human neurofibromin occur in the N-terminal half of the protein, with 16 changes clustered just upstream of the IRA-related segment. Given the high degree of sequence identity, virtually any sequence alteration in NF1 patients or tumors is potentially significant. We have also found that the 3' untranslated segment of NF1 mRNA is highly conserved, suggesting that this region may also be a target for mutations in NF1 patients. |
