Waksman Institute and Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ 08854, USA.
Development. 2024 Dec 1;151(23). doi: 10.1242/dev.202919. Epub 2024 Nov 29.
The protocadherins Fat and Dachsous regulate organ growth, shape, patterning, and planar cell polarity. Although Dachsous and Fat have been described as ligand and receptor, respectively, in a signal transduction pathway, there is also evidence for bidirectional signaling. Here, we assess signaling downstream of Dachsous through analysis of its intracellular domain. Genomic deletions of conserved sequences within dachsous identified regions of the intracellular domain that contribute to Dachsous activity. Deletion of the A motif increased Dachsous protein levels and decreased wing size. Deletion of the D motif decreased Dachsous levels at cell membranes, increased wing size, and disrupted wing, leg and hindgut patterning and planar cell polarity. Co-immunoprecipitation experiments established that the D motif is necessary and sufficient for association of Dachsous with key partners, including Lowfat, Dachs, Spiny-legs, Fat and MyoID. Subdivision of the D motif identified distinct regions that preferentially contribute to different Dachsous activities. Our results identify motifs that are essential for Dachsous function and are consistent with the hypothesis that the key function of Dachsous is regulation of Fat.
原钙黏蛋白 Fat 和 Dachsous 调节器官生长、形状、图案和平面细胞极性。尽管 Dachsous 和 Fat 分别被描述为信号转导途径中的配体和受体,但也有双向信号的证据。在这里,我们通过分析 Dachsous 的细胞内结构域来评估 Dachsous 的下游信号。 Dachsous 内保守序列的基因组缺失鉴定出细胞内结构域的区域,这些区域对 Dachsous 的活性有贡献。A 基序的缺失增加了 Dachsous 蛋白水平并减小了翅膀大小。D 基序的缺失减少了 Dachsous 在细胞膜上的水平,增加了翅膀大小,并破坏了翅膀、腿和后肠的图案和平面细胞极性。共免疫沉淀实验表明,D 基序对于 Dachsous 与包括 Lowfat、Dachs、Spiny-legs、Fat 和 MyoID 在内的关键伙伴的结合是必需的和充分的。D 基序的细分确定了优先促进不同 Dachsous 活性的不同区域。我们的结果确定了 Dachsous 功能所必需的基序,这与 Dachsous 的关键功能是调节 Fat 的假说一致。