Loss of connexin43-mediated gap junctional coupling in the mesenchyme of limb buds leads to altered expression of morphogens in mice
Authors: Dobrowolski, Radoslaw; Hertig, Gerda; Lechner, Hildegard; Wrsdrfer, Philipp; Wulf, Volker; Dicke, Nikolai; Eckert, Dawid; Bauer, Reinhard; Schorle, Hubert; Willecke, Klaus
Source: Human Molecular Genetics, Volume 18, Number 15, 1 August 2009 , pp. 2899-2911(13)
Publisher: Oxford University Press
Abstract:Mutations in the GJA1 gene coding for connexin43 (Cx43) cause oculodentodigital dysplasia (ODDD), a pleiotropic human disorder with characteristic morphologic anomalies of face, teeth, bones and digits. Interdigital webbings, also called syndactylies, are a characteristic phenotype of this disease showing high intra- and interfamilial penetrance. Therefore, we decided to study the molecular basis of syndactylies caused by Cx43 mutations. In order to reveal the impact of Cx43-mediated gap junctional coupling, we used mice expressing the human point mutation Cx43G138R and, in addition, knock-out mice lacking Cx43. Both conditional mouse models developed syndactylies as a consequence of disturbed interdigital apoptosis, which we show to be due to reduced expression of two key morphogens: sonic hedgehog (Shh) and bone morphogenic protein 2 (Bmp2). Diminished levels of Bmp2 and subsequent up-regulation of fibroblast growth factors (Fgfs) lead to an insufficient induction of interdigital apoptosis. Interestingly, the reduction of Shh expression in Cx43 mutants begins on embryonic day 10.5 indicating a disturbance of the Fgf/Shh regulatory feedback loop, and confirming the recently published observation that gap junctions can relay Fgf signals to neighboring cells. Thus, Cx43-mediated gap junctional coupling in the mesenchyme of limb buds after ED11 is essential to maintain Shh expression, which regulates the downstream signaling of Bmp2. Besides diminished interdigital apoptosis, the decreased expression of Bmp2 in Cx43 mutants may also be involved in other morphological alterations in patients suffering from ODDD.
Document Type: Research Article
Publication date: 2009-08-01
- Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics.
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- By this author: Dobrowolski, Radoslaw ; Hertig, Gerda ; Lechner, Hildegard ; Wrsdrfer, Philipp ; Wulf, Volker ; Dicke, Nikolai ; Eckert, Dawid ; Bauer, Reinhard ; Schorle, Hubert ; Willecke, Klaus