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黏附 GPCR Adgrg6(Gpr126):来自斑马鱼模型的见解。

The adhesion GPCR Adgrg6 (Gpr126): Insights from the zebrafish model.

机构信息

Department of Biomedical Science, Bateson Centre and Neuroscience Institute, University of Sheffield, Sheffield, UK.

Sosei Heptares, Steinmetz Building, Granta Park, Cambridge, UK.

出版信息

Genesis. 2021 Apr;59(4):e23417. doi: 10.1002/dvg.23417. Epub 2021 Mar 18.

Abstract

Adhesion GPCRs are important regulators of conserved developmental processes and represent an untapped pool of potential targets for drug discovery. The adhesion GPCR Adgrg6 (Gpr126) has critical developmental roles in Schwann cell maturation and inner ear morphogenesis in the zebrafish embryo. Mutations in the human ADGRG6 gene can result in severe deficits in peripheral myelination, and variants have been associated with many other disease conditions. Here, we review work on the zebrafish Adgrg6 signaling pathway and its potential as a disease model. Recent advances have been made in the analysis of the structure of the Adgrg6 receptor, demonstrating alternative structural conformations and the presence of a conserved calcium-binding site within the CUB domain of the extracellular region that is critical for receptor function. Homozygous zebrafish adgrg6 hypomorphic mutants have been used successfully as a whole-animal screening platform, identifying candidate molecules that can influence signaling activity and rescue mutant phenotypes. These compounds offer promise for further development as small molecule modulators of Adgrg6 pathway activity.

摘要

黏附 GPCR 是保守发育过程的重要调节剂,代表了药物发现的潜在靶点的未开发池。黏附 GPCR Adgrg6(Gpr126)在斑马鱼胚胎中的施万细胞成熟和内耳形态发生中具有关键的发育作用。人类 ADGRG6 基因突变可导致周围髓鞘严重缺失,并且变体与许多其他疾病状况有关。在这里,我们回顾了斑马鱼 Adgrg6 信号通路及其作为疾病模型的潜力。最近在 Adgrg6 受体结构的分析方面取得了进展,证明了存在替代的结构构象和在细胞外区域的 CUB 结构域内存在保守的钙结合位点,这对于受体功能至关重要。杂合斑马鱼 adgrg6 功能缺失突变体已成功用作全动物筛选平台,鉴定出可影响信号活性并挽救突变表型的候选分子。这些化合物有望进一步开发为 Adgrg6 途径活性的小分子调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bff2/11475505/ce0d359881f7/DVG-59-e23417-g001.jpg

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