Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome.

Published

Journal Article

The syndrome of congenital hypoparathyroidism, mental retardation, facial dysmorphism and extreme growth failure (HRD or Sanjad-Sakati syndrome; OMIM 241410) is an autosomal recessive disorder reported almost exclusively in Middle Eastern populations. A similar syndrome with the additional features of osteosclerosis and recurrent bacterial infections has been classified as autosomal recessive Kenny-Caffey syndrome (AR-KCS; OMIM 244460). Both traits have previously been mapped to chromosome 1q43-44 (refs 5,6) and, despite the observed clinical variability, share an ancestral haplotype, suggesting a common founder mutation. We describe refinement of the critical region to an interval of roughly 230 kb and identification of deletion and truncation mutations of TBCE in affected individuals. The gene TBCE encodes one of several chaperone proteins required for the proper folding of alpha-tubulin subunits and the formation of alpha-beta-tubulin heterodimers. Analysis of diseased fibroblasts and lymphoblastoid cells showed lower microtubule density at the microtubule-organizing center (MTOC) and perturbed microtubule polarity in diseased cells. Immunofluorescence and ultrastructural studies showed disturbances in subcellular organelles that require microtubules for membrane trafficking, such as the Golgi and late endosomal compartments. These findings demonstrate that HRD and AR-KCS are chaperone diseases caused by a genetic defect in the tubulin assembly pathway, and establish a potential connection between tubulin physiology and the development of the parathyroid.

Full Text

Duke Authors

Cited Authors

  • Parvari, R; Hershkovitz, E; Grossman, N; Gorodischer, R; Loeys, B; Zecic, A; Mortier, G; Gregory, S; Sharony, R; Kambouris, M; Sakati, N; Meyer, BF; Al Aqeel, AI; Al Humaidan, AK; Al Zanhrani, F; Al Swaid, A; Al Othman, J; Diaz, GA; Weiner, R; Khan, KTS; Gordon, R; Gelb, BD; HRD/Autosomal Recessive Kenny-Caffey Syndrome Consortium,

Published Date

  • November 2002

Published In

Volume / Issue

  • 32 / 3

Start / End Page

  • 448 - 452

PubMed ID

  • 12389028

Pubmed Central ID

  • 12389028

Electronic International Standard Serial Number (EISSN)

  • 1546-1718

International Standard Serial Number (ISSN)

  • 1061-4036

Digital Object Identifier (DOI)

  • 10.1038/ng1012

Language

  • eng