Polyglutamine repeat length influences human androgen receptor/c-Jun mediated transcription

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17 Citations (Scopus)

Abstract

The androgen receptor and c-Jun are known to interact to modulate each others transcriptional activities. The androgen receptor contains a polymorphic polyglutamine repeat and expansion of this repeat to beyond approximately 40 causes spinobulbar muscular atrophy (SBMA; also known as Kennedy's disease), a genetic form of motor neurone disease. Here we show that the size of this polyglutamine tract influences both c-Jun regulation of androgen receptor-mediated transcription and androgen receptor regulation of c-Jun activity. c-Jun is a key mediator of neuronal survival and death by apoptosis. Inappropriate interactions between c-Jun and androgen receptors containing pathological length glutamine repeats may therefore be part of the pathogenic process in SBMA. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)9 - 12
Number of pages4
JournalNeuroscience Letters
Volume277
Issue number1
DOIs
Publication statusPublished - 17 Dec 1999

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