Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.
Invest Ophthalmol Vis Sci
; 46(12): 4671-83, 2005 Dec.
Article
em En
| MEDLINE
| ID: mdl-16303964
ABSTRACT
PURPOSE:
To characterize three new mouse small-eye mutants detected during ethylnitrosourea mutagenesis programs.METHODS:
Three new mouse small-eye mutants were morphologically characterized, particularly by in situ hybridization. The mutations were mapped, and the candidate gene was sequenced. The relative amount of Pax6-specific mRNA was determined by real-time PCR. Reporter gene analysis used Crygf and Six3 promoter fragments in front of a luciferase gene and HEK293 cells as recipients.RESULTS:
The new mutations--ADD4802, Aey11, and Aey18--were mapped to chromosome 2; causative mutations have been characterized in Pax6 (Aey11 C-->T substitution in exon 8, creating a stop codon just in front of the homeobox; ADD4802 G-->A substitution at the beginning of intron 8 changes splicing and leads to an altered open reading frame and then to a premature stop codon; Aey18 G-->A exchange in the last base of intron 5a leads also to a splice defect, skipping exons 5a and 6). Real-time PCR indicated nonsense-mediated decay in Pax6Aey11 and Pax6Aey18 mutants but not in Pax6ADD4802. This result is supported by the functional analysis of corresponding expression constructs in cell culture, where the Aey11 and Aey18 alleles did not show a stimulation of the Six3 promotor or an inhibition of the Crygf promoter (as wild-type constructs do). However, the Pax6ADD4802 allele stimulated both promoters.CONCLUSIONS:
Together with functional analysis in a reporter gene assay and immunohistochemistry using Pax6 antibodies, it is suggested that the Pax6Aey11 and Pax6Aey18 alleles act through a loss of function, whereas ADD4802 represents a gain-of-function allele.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Proteínas Repressoras
/
Microftalmia
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Regiões Promotoras Genéticas
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Proteínas de Homeodomínio
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Alelos
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Fatores de Transcrição Box Pareados
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Proteínas do Olho
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Mutação
Limite:
Animals
Idioma:
En
Ano de publicação:
2005
Tipo de documento:
Article