Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin.

Hennies HC, Kornak U, Zhang H, Egerer J, Zhang X, Seifert W, Kühnisch J, Budde B, Nätebus M, Brancati F, Wilcox WR, Müller D, Kaplan PB, Rajab A, Zampino G, Fodale V, Dallapiccola B, Newman W, Metcalfe K, Clayton-Smith J, Tassabehji M, Steinmann B, Barr FA, Nürnberg P, Wieacker P, Mundlos S

Forschungsartikel (Zeitschrift)

Zusammenfassung

Gerodermia osteodysplastica is an autosomal recessive disorder characterized by wrinkly skin and osteoporosis. Here we demonstrate that gerodermia osteodysplastica is caused by loss-of-function mutations in SCYL1BP1, which is highly expressed in skin and osteoblasts. The protein localizes to the Golgi apparatus and interacts with Rab6, identifying SCYL1BP1 as a golgin. These results associate abnormalities of the secretory pathway with age-related changes in connective tissues.

Details zur Publikation

FachzeitschriftNature Genetics (Nat Genet)
Jahrgang / Bandnr. / Volume40
Ausgabe / Heftnr. / Issue12
Seitenbereich1410-1412
StatusVeröffentlicht
Veröffentlichungsjahr2008
Sprache, in der die Publikation verfasst istEnglisch
StichwörterInfant; Chromosomes Human Pair 1. Male; rab GTP-Binding Proteins; Carrier Proteins; Pedigree; Bone Diseases; Female; Skin Diseases Genetic; Humans; Infant; Chromosomes Human Pair 1. Male; rab GTP-Binding Proteins; Carrier Proteins; Pedigree; Bone Diseases; Female; Skin Diseases Genetic; Humans

Autor*innen der Universität Münster

Wieacker, Peter
Klinik für Medizinische Genetik
Zhang, Haiming
Arbeitsgruppe Grenzflächenphysik (Prof. Fuchs)