Discovery - University of Dundee - Online Publications

Library & Learning Centre

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

Research output: Contribution to journalArticle

View graph of relations

Authors

  • Elizabeth Pohler
  • Ons Mamai
  • Jennifer Hirst
  • Mozheh Zamiri
  • Helen Horn
  • Toshifumi Nomura
  • Alan D Irvine
  • Benvon Moran
  • Neil J Wilson
  • Frances J D Smith
  • Christabelle S M Goh
  • Aileen Sandilands
  • Christian Cole
  • Geoffrey J Barton
  • Alan T Evans
  • Hiroshi Shimizu
  • Masashi Akiyama
  • Mitsuhiro Suehiro
  • Izumi Konohana
  • Mohammad Shboul
  • Sebastien Teissier
  • Lobna Boussofara
  • Mohamed Denguezli
  • Ali Saad
  • Moez Gribaa
  • Patricia J Dopping-Hepenstal
  • John A McGrath
  • David R Goudie
  • Bruno Reversade
  • Colin S Munro
  • W H Irwin McLean (Lead / Corresponding author)

Research units

Info

Original languageEnglish
Pages1272-1276
Number of pages5
JournalNature Genetics
Journal publication dateNov 2012
Journal number11
Volume44
DOIs
StatePublished

Abstract

Palmoplantar keratodermas (PPKs) are a group of disorders that are diagnostically and therapeutically problematic in dermatogenetics. Punctate PPKs are characterized by circumscribed hyperkeratotic lesions on the palms and soles with considerable heterogeneity. In 18 families with autosomal dominant punctate PPK, we report heterozygous loss-of-function mutations in AAGAB, encoding a- and ?-adaptin-binding protein p34, located at a previously linked locus at 15q22. a- and ?-adaptin-binding protein p34, a cytosolic protein with a Rab-like GTPase domain, was shown to bind both clathrin adaptor protein complexes, indicating a role in membrane trafficking. Ultrastructurally, lesional epidermis showed abnormalities in intracellular vesicle biology. Immunohistochemistry showed hyperproliferation within the punctate lesions. Knockdown of AAGAB in keratinocytes led to increased cell division, which was linked to greatly elevated epidermal growth factor receptor (EGFR) protein expression and tyrosine phosphorylation. We hypothesize that p34 deficiency may impair endocytic recycling of growth factor receptors such as EGFR, leading to increased signaling and cellular proliferation.

Documents

Library & Learning Centre

Contact | Accessibility | Policy