Disruption of tuftelin 1, a desmosome associated protein, causes skin fragility, woolly hair and palmoplantar keratoderma

Desmosomes are dynamic complex protein structures involved in cellular adhesion. Disruption of these structures by loss of function variants in desmosomal genes lead to a variety of skin and heart related phenotypes. Here, we report tuftelin 1 as a desmosome-associated protein, implicated in epidermal integrity. In two siblings with mild skin fragility, woolly hair and mild palmoplantar keratoderma, but without a cardiac phenotype, we identified a homozygous splice site variant in the TUFT1 gene, leading to aberrant mRNA splicing and loss of tuftelin 1 protein. Patients' skin and keratinocytes showed acantholysis, perinuclear retraction of intermediate filaments, and reduced mechanical stress resistance. Immunolabeling and transfection studies showed that tuftelin 1 is positioned within the desmosome and its location dependent on the presence of the desmoplakin carboxy-terminal tail. A Tuft1 knock-out mouse model mimicked the patients' phenotypes. Altogether, this study reveals tuftelin 1 as a desmosome-associated protein, whose absence causes skin fragility, woolly hair and palmoplantar keratoderma

MSJ777202_supplementary_data – Supplemental material for Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family

<p>Supplemental material, MSJ777202_supplementary_data for Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family by Julia Y Mescheriakova, Annemieke JMH Verkerk, Najaf Amin, André G Uitterlinden, Cornelia M van Duijn and Rogier Q Hintzen in Multiple Sclerosis Journal</p