Gα 亚基 Gq/11 家族是下颌骨发育的必要条件和充分条件

Stanley M. Kanai, Chloe R. Garcia, MaCalia R. Augustus, Shujan A. Sharafeldeen, Elliott P. Brooks, Juliana Sucharov, Ezra S. Lencer, James T. Nichols, David E. Clouthier
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摘要

脊椎动物的颌骨发育是由高度保守的配体-受体系统协调的,如多肽配体内皮素 1(Edn1)和 A 型内皮素受体(Ednra),它们是下颌骨结构模式化所必需的。Edn1/Ednra信号通路通过调节大量模式基因的表达来确定下颌骨祖细胞的特征,但人们对将受体激活与基因调节联系起来的细胞内信号机制仍然知之甚少。作为阐明这一机制的第一步,我们利用药物抑制和基因消减 Gq/11 活性以及在 edn1-/- 胚胎中转基因诱导组成型活性 Gq 蛋白的方法,研究了斑马鱼体内 Gα 亚基 Gq/11 家族的功能。遗传性 Gq/11 活性缺失完全重现了 edn1-/- 表型,其中编码 G11 的基因最为关键。此外,在edn1-/-胚胎中诱导Gq活性不仅能恢复依赖于Edn1/Ednra的颌骨结构和基因表达特征,还能使上颌骨结构同化为类似下颌骨的结构。这些结果表明,Gq/11是斑马鱼Ednra下颌模式化机制的必要和充分中介。
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The Gq/11 family of Gα subunits is necessary and sufficient for lower jaw development
Vertebrate jaw development is coordinated by highly conserved ligand-receptor systems such as the peptide ligand Endothelin 1 (Edn1) and Endothelin receptor type A (Ednra), which are required for patterning of lower jaw structures. The Edn1/Ednra signaling pathway establishes the identity of lower jaw progenitor cells by regulating expression of numerous patterning genes, but the intracellular signaling mechanisms linking receptor activation to gene regulation remain poorly understood. As a first step towards elucidating this mechanism, we examined the function of the Gq/11 family of Gα subunits in zebrafish using pharmacological inhibition and genetic ablation of Gq/11 activity and transgenic induction of a constitutively active Gq protein in edn1-/- embryos. Genetic loss of Gq/11 activity fully recapitulated the edn1-/- phenotype, with genes encoding G11 being most essential. Furthermore, inducing Gq activity in edn1-/- embryos not only restored Edn1/Ednra-dependent jaw structures and gene expression signatures but also caused homeosis of the upper jaw structure into a lower jaw-like structure. These results indicate that Gq/11 is necessary and sufficient to mediate the lower jaw patterning mechanism for Ednra in zebrafish.
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