Drosophila homolog of the myotonic dystrophy-associated gene, SIX5, is required for muscle and gonad development

R J Kirby, G M Hamilton, D J Finnegan, K J Johnson, A P Jarman

Research output: Contribution to journalArticlepeer-review

Abstract

SIX5 belongs to a Family of highly conserved: homeodomain transcription factors implicated in development and disease [1-3]. The mammalian SIX5/SIX4 gene pair is likely to be involved in the development of mesodermal structures [4-6]. Moreover, a variety of data have implicated human SIX5 dysfunction as a contributor to myotonic dystrophy type 1 (DM1), a condition characterized by a number of pathologies including muscle defects and testicular atrophy [7-9]. However, this link remains controversial. Here, we investigate the Drosophila gene, D-Six4, which is the closest homolog to SIX5 of the three Drosophila Six family members [10]. We show by mutant analysis-that D-Six4 is required for the normal development of muscle and the mesodermal component of the gonad. Moreover, adult males with defective D-Six4 genes exhibit testicular reduction. We propose that D-Six4 directly or indirectly regulates genes involved in the cell recognition events required for myoblast fusion and the germline:soma interaction. While the exact phenotypic relationship between D-Six4 and SIX4/5 remains to be elucidated, the defects in D-Six4 mutant flies suggest that human SIX5 should be more strongly considered as being responsible for the muscle wasting and testicular atrophy phenotypes in DM1.

Original languageEnglish
Pages (from-to)1044-1049
Number of pages6
JournalCurrent Biology
Volume11
Issue number13
Publication statusPublished - 10 Jul 2001

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