Chen Yuting, Knezevic Vladimir, Ervin Valerie, Hutson Richard, Ward Yvona, Mackem Susan
Laboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, MD 20892, USA.
Development. 2004 May;131(10):2339-47. doi: 10.1242/dev.01115. Epub 2004 Apr 21.
Sonic hedgehog (Shh) signaling regulates both digit number and identity, but how different distinct digit types (identities) are specified remains unclear. Shh regulates digit formation largely by preventing cleavage of the Gli3 transcription factor to a repressor form that shuts off expression of Shh target genes. The functionally redundant 5'Hoxd genes regulate digit pattern downstream of Shh and Gli3, through as yet unknown targets. Enforced expression of any of several 5'Hoxd genes causes polydactyly of different distinct digit types with posterior transformations in a Gli3(+) background, whereas, in Gli3 null limbs, polydactylous digits are all similar, short and dysmorphic, even though endogenous 5'Hoxd genes are broadly misexpressed. We show that Hoxd12 interacts genetically and physically with Gli3, and can convert the Gli3 repressor into an activator of Shh target genes. Several 5'Hoxd genes, expressed differentially across the limb bud, interact physically with Gli3. We propose that a varying [Gli3]:[total Hoxd] ratio across the limb bud leads to differential activation of Gli3 target genes and contributes to the regulation of digit pattern. The resulting altered balance between 'effective' Gli3 activating and repressing functions may also serve to extend the Shh activity gradient spatially or temporally.
音猬因子(Shh)信号通路调控着手指的数量和特征,但不同类型(特征)的手指是如何被指定的仍不清楚。Shh主要通过阻止Gli3转录因子裂解为一种抑制形式来调节手指形成,这种抑制形式会关闭Shh靶基因的表达。功能冗余的5'Hoxd基因通过尚未明确的靶点在Shh和Gli3的下游调控手指模式。在Gli3(+)背景下,强制表达几种5'Hoxd基因中的任何一种都会导致不同类型手指出现多指畸形并伴有向后的转变,而在Gli3基因敲除的肢体中,多指的手指都相似、短小且形态异常,尽管内源性5'Hoxd基因广泛地表达异常。我们发现Hoxd12在遗传和物理层面上与Gli3相互作用,并能将Gli3抑制因子转化为Shh靶基因的激活因子。几种在肢体芽中差异表达的5'Hoxd基因在物理层面上与Gli3相互作用。我们提出,肢体芽中[Gli3]:[总Hoxd]比例的变化会导致Gli3靶基因的差异激活,并有助于调节手指模式。“有效”的Gli3激活和抑制功能之间由此产生的平衡改变,也可能在空间或时间上扩展Shh活性梯度。