The present invention relates to the identification of loss-of-function mutations in the filaggrin gene and their use in diagnosing ichthyosis vulgaris and/or susceptibility to other diseases including atopic dermatitis (eczema), asthma, psoriasis and allergies (including food allergy).
1. A method for detecting ichthyosis vulgaris or a predisposition to ichthyosis vulgaris in a human subject comprising the step of:
detecting in a sample of nucleic acid from the subject the presence of a R501X mutation in the filaggrin gene using one or more of the primers selected from SEQ ID NO: 9, 10, 11, or 12; and
correlating the presence of the R501X mutation in the sample with detection of ichthyosis vulgaris or a predisposition to ichthyosis vulgaris in the subject.
2. A method for detecting atopic dermatitis or asthma in a human subject comprising the step of:
detecting in a sample of nucleic acid from the subject the presence of a R501X mutation in the filaggrin gene using one or more of the primers selected from SEQ ID NO: 9, 10, 11, or 12; and
correlating the presence of the R501X mutation in the sample with detection of atopic dermatitis or asthma in the subject.
3. The method according to claim 1 , wherein the nucleic acid is genomic DNA or mRNA.
4. The method according to claim 1 , wherein the human subject is a newborn or a fetus.
5. The method according to claim 1 , wherein the detection step comprises an analysis technique selected from the group consisting of: quantitative PCR, semi-quantitative PCR, real-time PCR, nucleic acid sequencing, hybridization studies, and restriction fragment length polymorphism (RFLP) analysis.
6. The method according to claim 1 , further comprising a step of identifying the number of filaggrin repeats in the filaggrin gene from the sample.
7. The method according to claim 2 , wherein the nucleic acid is genomic DNA or mRNA.
8. The method according to claim 2 , wherein the human subject is a newborn or a fetus.
9. The method according to claim 2 , wherein the detection step comprises an analysis technique selected from the group consisting of: quantitative PCR, semi-quantitative PCR, real-time PCR, nucleic acid sequencing, hybridization studies, and restriction fragment length polymorphism (RFLP) analysis.
10. The method according to claim 2 , further comprising a step of identifying the number of filaggrin repeats in the filaggrin gene from the sample.