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Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy

Research output: Contribution to journalArticle

  • Carol-Anne Martin
  • Ilyas Ahmad
  • Muhammad Sajid Hussain
  • Andrea Leitch
  • Gudrun Nürnberg
  • Mohammad Reza Toliat
  • Fawad Khan
  • Zafar Ali
  • Sigrid Tinschert
  • James Ding
  • Charlotte Keith
  • Margaret E Harley
  • Rolf Müller
  • Ingrid Hoffmann
  • Valérie Cormier Daire
  • Hélène Dollfus
  • Lucie Dupuis
  • Anu Bashamboo
  • Kenneth McElreavey
  • Ariana Kariminejad
  • Roberto Mendoza-Londono
  • Anthony T Moore
  • Anand Saggar
  • Catie Schlechter
  • Richard Weleber
  • Holger Thiele
  • Janine Altmüller
  • Wolfgang Höhne
  • Matthew E Hurles
  • Angelika Anna Noegel
  • Shahid Mahmood Baig
  • Peter Nürnberg

Related Edinburgh Organisations

Original languageEnglish
Pages (from-to)1283–1292
JournalNature Genetics
Volume46
DOIs
Publication statusPublished - 26 Oct 2014

Abstract

Centrioles are essential for ciliogenesis. However, mutations in centriole biogenesis genes have been reported in primary microcephaly and Seckel syndrome, disorders without the hallmark clinical features of ciliopathies. Here we identify mutations in the genes encoding PLK4 kinase, a master regulator of centriole duplication, and its substrate TUBGCP6 in individuals with microcephalic primordial dwarfism and additional congenital anomalies, including retinopathy, thereby extending the human phenotypic spectrum associated with centriole dysfunction. Furthermore, we establish that different levels of impaired PLK4 activity result in growth and cilia phenotypes, providing a mechanism by which microcephaly disorders can occur with or without ciliopathic features.

ID: 18459058