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Characterisation of filaggrin gene and results of mutation screening. Louise McClelland 13 th October 2010. Key words. Filaggrin Polyprotein profilaggrin Epidermal differentiation cDNA library Somatic hybrids M13 sequencing Long range PCR Ichthyosis vulgaris
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Characterisation of filaggrin gene and results of mutation screening Louise McClelland 13th October 2010
Key words • Filaggrin • Polyprotein profilaggrin • Epidermal differentiation • cDNAlibrary • Somatic hybrids • M13 sequencing • Long range PCR • Ichthyosis vulgaris • Atopic dermatitis (eczema) • Asthma • Ancient mutations
Filaggrin Overview • Filaggrin protein • Processing and function • Gene ID and characterisation • Mutation analysis
Filaggrin protein • Filaggrin is synthesised as a giant precursor protein, profilaggrin • Filament-aggregating protein • Interact with keratin intermediate filaments in terminally differentiating mammalian epidermis • Very important in facilitating epidermal differentiation and maintaining skin barrier function • Implicated in a no. of keratinizing disorders
Time line 1980 1990 2000 2010 • 1981 - Term Filaggrin (FLG) coined • Described a class of structural proteins that have been isolated from the stratum corneum • 1984-1985 – Filaggrin and profilaggrin protein characterisation • 1989 – FLG gene cloned and mapped • 1992-1993 Gene characterisation • 2006 – LOF mutations ID’d in ichthyosis vulgaris and atopic dermatitis • 2007 – Further mutation analysis
Profilaggrin polyprotein 1980 1990 2000 2010 • >400 kDa • N-terminal domain • 2 subdomains • ?role in regulation of profilaggrin by Ca2+ • Repeat region • 10-12 tandemly arranged filaggrin repeats • Linker regions between repeats • C-terminal domain 1984-1985
Profilaggrin processing • During terminal differentiation of granular cells profilaggrin is proteolytically cleaved into; • Multiple 37 kDa (342 AA) filaggrin peptides • N and C domains • Linker regions between repeats • Phosphorylation of profilaggrin believed to prevent premature cleavage
Filaggrin • Aggregates to keratin intermediate filaments in cytoskeleton • Creates a dense insoluble protein-lipid keratin matrix cross linked by transgluaminases • Causes collapse of granular cells into flattened anuclear squames • Scaffold for the attachment of cornified cell envelope (CCE) proteins and lipids • CCE • Outermost barrier layer of skin • Prevents water loss • Impedes allergens, toxic chemicals and infectious agents
Filaggrin processing in squames • Post translational conversion of arginine to citrulline (Deimination/citrulination) • Promotes unfolding and degradation into hygroscopic AA and derivatives • Contributes to Natural moisturising factor (NMF) • NMF responsible for maintaining hydration in low environment humidity
ID of filaggrin gene 1980 1990 2000 2010 • Differences between mouse and human FLG complicated ID • Anti-mouse FLG antibodies do not recognise human FLG • cDNA clones encoding mouse FLG do not recognise human FLG • cDNA library of human foreskin epidermal tissue created in a λ phage • Screened library using human anti-filaggrin monoclonal antibody • Antibody positive clones purified from plaques (12 clones) 1989
DNA libraries Griffiths, 1999
M13 mediated sequencing • cDNA inserted into M13 vectors Strachan and Read, 2010
Longest clone contained ORF of 416 AA • Beginning and end share homology • Showed encodes a polyprotein precursor of filaggrin • Identified linker sequences are removed to create monomers
Mapping 1 • Somatic cell hybrids • Recorded what human chromosomes retained in each hybrid • Examined hybrids DNA by Southern blot • Filaggrin sequence probe • Only hybrids retaining chromosome 1 Griffiths, 1999
Mapping 2 • RNA probes for in situ hybridisation • Synthesised from earlier plaques (in pGEM-3B vector) • Refined chromosomal position to 1q
characterisation 1980 1990 2000 2010 • Cloned profilaggrin cDNA was compared to genomic profilaggrin to identify the exon/intron boundaries • Contains 3 exons 1992-1993
Dry, flaky skin Mutation screening 1980 1990 2000 2010 • First investigated in ichthyosis vulgaris (IV) • Most common and mildest ichthyosis • Poorly formed stratum corneum prone to water loss • Predisposition to eczema and associated asthma Palmar hyperlinearity of palms and soles Keratosis pilaris Smith et al., 2006 2006
FLG mutations suspected in IV because; • Absence of filaggrin in keratinocytes of IV patients by immunoblotting • Decreased FLG mRNA • Recessive mouse model flaky tail (ft) • Histologically similar to IV • Strong genetic linkage to mouse FLG locus • IV linkage to 1q21 in an American family
FLG Mutation screening:Ichthyosis vulgaris • 15 kindred examined • Irish, Scottish and Americans of European decent • Long range PCR of FLG • R501X • 2284del4 • Both cause PTC in 1st filaggrin repeat • Semi dominant inheritance • Heterozygotes = mild phenotype • Homozygotes = severe phenotype • Noted several patients had atopic dermatitis and a few had asthma Allele F = ~4% in European ancestry
Atopic disease (AD) • Atopic dermatitis (eczema) • Allergies • Asthma • FLG mutations suspected in atopic disease because of link between IV and eczema
FLG Mutation screening:Atopic Disease 1980 1990 2000 2010 • Identified R501X and 2284del4 mutations in atopic disease • Significant association between these mutations and; • Atopic dermatitis • Asthma in the context of atopic dermatitis • Carried by 9% of people of European origin 2006 Palmer et al., 2006
Further analysis 1980 1990 2000 2010 • Several mutations now identified • All common mutations null mutants • Other populations with FLG mutations identified • Japanese, Mexican, Basque, Indian • Distinct haplotypes associated with some mutations • R501X, 2284del4, R2447X, S3247X • R501X and 2284del4 absent from non-Europeans • Ancient mutations • Similar pathogenicity of 3’ mutations as 5’ • Immunoblotting showed still greatly reduced filaggrin 2007 Sandilands et al., 2007
conclusions • Major predisposing gene for atopic disease • Complex disease model emerging • Refocused attention on skin barrier rather than immunity in eczema research • FLG mutations may be modifying factors in other conditions • E.g. X-linked ichthyosis • Reduced no. of FLG repeats may predispose to dry skin • Hypothesis of why mutations so common in Europe (particularly Ireland) • Mutation advantage at some point in history • Allows a degree of natural vaccination against antigens e.g. plague • Identifying when the mutations arose may help explain why so prevalent
References • Brown, Genome, BIOS, 1st edition, 1999 • Griffiths et al., Modern Genetic Analysis, Freeman and Co. NY, 1st edition, 1999 • McKinley-Grant et al, PNAS86: 4848-4852; 1989 • Palmer et al., Nat Genet38: 441-446; 2006 • Presland et al., J Biol Chem 267: 23772-23781; 1992 • Sandilands et al., Nat Genet 39: 650-654; 2007 • Sandilands et al., J Cell Sci122: 1285-1294; 2009 • Good review • Smith et al., Nat Genet38: 337; 2006 • Steinert et al., PNAS78: 4097-4101; 1981 • Strachan and Read, Human Molecular Genetics, Garland Science, 4th edition, 2010