Molecular Characterization of Pax6^2Neu Through Pax6^10Neu: An Extension of the Pax6 Allelic Series and the Identification of Two Possible Hypomorph Alleles in the Mouse Mus musculus

Corresponding author: Jack Favor, Institute of Mammalian Genetics, GSF-Research Center for Environment and Health, Ingolstädter Landstr. 1, D-85764, Neuherberg, Germany., favor{at}gsf.de (E-mail)

Communicating editor: C. KOZAK

Phenotype-based mutagenesis experiments will increase the mouse mutant resource, generating mutations at previously unmarked loci as well as extending the allelic series at known loci. Mapping, molecular characterization, and phenotypic analysis of nine independent Pax6 mutations of the mouse recovered in mutagenesis experiments is presented. Seven mutations result in premature termination of translation and all express phenotypes characteristic of null alleles, suggesting that Pax6 function requires all domains to be intact. Of major interest is the identification of two possible hypomorph mutations: Heterozygotes express less severe phenotypes and homozygotes develop rudimentary eyes and nasal processes and survive up to 36 hr after birth. Pax6^4Neu results in an amino acid substitution within the third helix of the homeodomain. Three-dimensional modeling indicates that the amino acid substitution interrupts the homeodomain recognition -helix, which is critical for DNA binding. Whereas cooperative dimer binding of the mutant homeodomain to a paired-class DNA target sequence was eliminated, weak monomer binding was observed. Thus, a residual function of the mutated homeodomain may explain the hypomorphic nature of the Pax6^4Neu allele. Pax6^7Neu is a base pair substitution in the Kozak sequence and results in a reduced level of Pax6 translation product. The Pax6^4Neu and Pax6^7Neu alleles may be very useful for gene-dosage studies.

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