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Mouse model of a human neurological disorder

Neurofibromatosis type 1 (NF1) is an inherited neurological disorder that affects 1 in 3,500 people worldwide. It is caused by mutations in the NF1 gene, which encodes neurofibromin, a protein involved in the Ras signalling pathway. Patients have tumours of neural origin and many have learning difficulties.Previous attempts to knock out the NF1 gene have been unsuccessful because the mutant mice die as embryos. Now, a team of researchers led by Luis Parada of the University of Texas Southwestern

Kenneth Lee(kenlee_fr@yahoo.fr)

Neurofibromatosis type 1 (NF1) is an inherited neurological disorder that affects 1 in 3,500 people worldwide. It is caused by mutations in the NF1 gene, which encodes neurofibromin, a protein involved in the Ras signalling pathway. Patients have tumours of neural origin and many have learning difficulties.

Previous attempts to knock out the NF1 gene have been unsuccessful because the mutant mice die as embryos. Now, a team of researchers led by Luis Parada of the University of Texas Southwestern Medical Center have generated mice in which an NF1 gene mutation is triggered only in neuronal cells. Reporting in the 1 April Genes and Development, Zhu et al inserted loxP sites flanking exons 31 and 32 of the mouse NF1 gene. By crossing these mice with a transgenic mouse strain that expresses Cre recombinase under the control of a neuronal-specific gene (Synapsin I), exons 31 and 32 of the...

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