Dachsous 细胞内结构域对 Dachsous-Fat 信号转导的贡献。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-11-05 DOI:10.1242/dev.202919
Bipin Kumar Tripathi, Kenneth D Irvine
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引用次数: 0

摘要

原粘连蛋白 Fat 和 Dachsous 调节器官的生长、形状、模式化和平面细胞极性。虽然 Dachsous 和 Fat 在信号转导途径中分别被描述为配体和受体,但也有证据表明信号是双向的。在这里,我们通过分析 Dachsous 的胞内结构域来评估其下游信号传导。通过基因组缺失 Dachsous 的保守序列,确定了有助于 Ds 活性的胞内结构域区域。A基序的缺失增加了Dachsous蛋白水平并缩小了翅膀尺寸。D motif的缺失降低了细胞膜上的Dachsous水平,增大了翅膀的尺寸,破坏了翅膀、腿和后肠的模式化以及平面细胞的极性。共免疫沉淀实验证实,D基序是Dachsous与Lowfat、Dachs、Spiny-legs、Fat和MyoID等关键伙伴结合的必要条件和充分条件。对 D 基序的细分发现了不同的区域,它们对不同的 Ds 活动有优先贡献。我们的研究结果确定了对 Dachsous 功能至关重要的图案,并与 Dachsous 的关键功能是调节 Fat 的假设相一致。
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Contributions of the Dachsous intracellular domain to Dachsous-Fat signaling.

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 Ds 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 Ds 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.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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