Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene

Cheryl Shoubridge, Desiree Cloosterman, Emma Parkinson-Lawerence, Douglas Brooks, Jozef Gécz

Research output: Contribution to journalArticle

35 Citations (Scopus)

Abstract

The Aristaless-related homeobox gene (ARX) is one of the major genes causing X-linked mental retardation. We have been interested in the pathogenic mechanism of expanded polyalanine tract mutations in ARX. We showed that the c.304ins(GCG)7 mutation causing an increase from 16 to 23 alanines increased the propensity of ARX protein aggregation and a shift from nuclear to cytoplasmic localization. We proposed that mislocalization of ARX via cytoplasmic aggregation and subsequent degradation leads to a partial loss of function, contributing to the pathogenesis. We identified importin 13 (IPO13), a mediator of nuclear import for a variety of proteins, as a novel ARX interacting protein. We predicted that the transport of ARX by IPO13 from the cytoplasm to the nucleus might be disrupted by expanded polyalanine tract mutations, but our data showed that in both yeast and mammalian cells these mutant ARX proteins were still able to interact with IPO13. We established the nuclear localization regions of the ARX homeodomain that were required for the interaction with IPO13 and correct localization of the full-length ARX transcription factor to the nucleus. Crown

LanguageEnglish
Pages59-71
Number of pages13
JournalGenomics
Volume90
Issue number1
DOIs
Publication statusPublished - 1 Jul 2007
Externally publishedYes

Keywords

  • ARX
  • Coimmunoprecipitation
  • Mutation
  • Nuclear localization sequence
  • Polyalanine tract
  • X-linked mental retardation
  • Yeast-2 hybrid

ASJC Scopus subject areas

  • Genetics

Cite this

Shoubridge, Cheryl ; Cloosterman, Desiree ; Parkinson-Lawerence, Emma ; Brooks, Douglas ; Gécz, Jozef. / Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene. In: Genomics. 2007 ; Vol. 90, No. 1. pp. 59-71.
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Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene. / Shoubridge, Cheryl; Cloosterman, Desiree; Parkinson-Lawerence, Emma; Brooks, Douglas; Gécz, Jozef.

In: Genomics, Vol. 90, No. 1, 01.07.2007, p. 59-71.

Research output: Contribution to journalArticle

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