Gamma-secretase gene mutations in familial acne inversa.

Article Details

Citation

Wang B, Yang W, Wen W, Sun J, Su B, Liu B, Ma D, Lv D, Wen Y, Qu T, Chen M, Sun M, Shen Y, Zhang X

Gamma-secretase gene mutations in familial acne inversa.

Science. 2010 Nov 19;330(6007):1065. doi: 10.1126/science.1196284. Epub 2010 Oct 7.

PubMed ID
20929727 [ View in PubMed
]
Abstract

Acne inversa (AI), also known as hidradenitis suppurativa, is a chronic, recurrent, inflammatory disease of hair follicles that often runs in families. We studied six Chinese families with features of AI as well as additional skin lesions on back, face, nape, and waist and found independent loss-of-function mutations in PSENEN, PSEN1, or NCSTN, the genes encoding essential components of the gamma-secretase multiprotein complex. Our results identify the gamma-secretase component genes as the culprits for a subset of familial AI, implicate the gamma-secretase-Notch pathway in the molecular pathogenesis of AI, and demonstrate that familial AI can be an allelic disorder of early-onset familial Alzheimer's disease.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Gamma-secretase subunit PEN-2Q9NZ42Details