Davey Megan G, Paton I Robert, Yin Yili, Schmidt Maike, Bangs Fiona K, Morrice David R, Smith Terence Gordon, Buxton Paul, Stamataki Despina, Tanaka Mikiko, Münsterberg Andrea E, Briscoe James, Tickle Cheryll, Burt Dave W
Division of Cell and Developmental Biology, Wellcome Trust Biocentre (WTB), University of Dundee, Dundee DD1 5EH, United Kingdom.
Genes Dev. 2006 May 15;20(10):1365-77. doi: 10.1101/gad.369106.
Talpid3 is a classical chicken mutant with abnormal limb patterning and malformations in other regions of the embryo known to depend on Hedgehog signaling. We combined the ease of manipulating chicken embryos with emerging knowledge of the chicken genome to reveal directly the basis of defective Hedgehog signal transduction in talpid3 embryos and to identify the talpid3 gene. We show in several regions of the embryo that the talpid3 phenotype is completely ligand independent and demonstrate for the first time that talpid3 is absolutely required for the function of both Gli repressor and activator in the intracellular Hedgehog pathway. We map the talpid3 locus to chromosome 5 and find a frameshift mutation in a KIAA0586 ortholog (ENSGALG00000012025), a gene not previously attributed with any known function. We show a direct causal link between KIAA0586 and the mutant phenotype by rescue experiments. KIAA0586 encodes a novel protein, apparently specific to vertebrates, that localizes to the cytoplasm. We show that Gli3 processing is abnormal in talpid3 mutant cells but that Gli3 can still translocate to the nucleus. These results suggest that the talpid3 protein operates in the cytoplasm to regulate the activity of both Gli repressor and activator proteins.
Talpid3是一种典型的鸡突变体,其肢体模式异常,胚胎其他区域存在畸形,已知这些区域依赖于刺猬信号通路。我们将操纵鸡胚胎的便利性与鸡基因组的新知识相结合,以直接揭示talpid3胚胎中刺猬信号转导缺陷的基础,并鉴定talpid3基因。我们在胚胎的几个区域表明,talpid3表型完全不依赖配体,并首次证明talpid3对于细胞内刺猬信号通路中Gli阻遏物和激活物的功能都是绝对必需的。我们将talpid3基因座定位到5号染色体,并在KIAA0586直系同源基因(ENSGALG00000012025)中发现一个移码突变,该基因以前未被赋予任何已知功能。我们通过拯救实验表明KIAA0586与突变体表型之间存在直接因果关系。KIAA0586编码一种新的蛋白质,显然是脊椎动物特有的,定位于细胞质。我们表明,在talpid3突变细胞中Gli3的加工异常,但Gli3仍可转运至细胞核。这些结果表明,talpid3蛋白在细胞质中发挥作用,以调节Gli阻遏物和激活物蛋白的活性。