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STRAD pseudokinases regulate axogenesis and LKB1 stability

机译:STRAD假激酶调节轴突生成和LKB1稳定性

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Background Neuronal polarization is an essential step of morphogenesis and connectivity in the developing brain. The serine/threonine kinase LKB1 is a key regulator of cell polarity, metabolism, tumorigenesis, and is required for axon formation. It is allosterically regulated by two related and evolutionarily conserved pseudokinases, STe20-Related ADapters (STRADs) α and β. The roles of STRADα and STRADβ in the developing nervous system are not fully defined, nor is it known whether they serve distinct functions. Results We find that STRADα is highly spliced and appears to be the primal STRAD paralog. We report that each STRAD is sufficient for axogenesis and promoting cell survival in the developing cortex. We also reveal a reciprocal protein-stabilizing relationship in vivo between LKB1 and STRADα, whereby STRADα specifically maintains LKB1 protein levels via cytoplasmic compartmentalization. Conclusions We demonstrate a novel role for STRADβ in axogenesis and also show for the first time in vivo that STRADα, but not STRADβ, is responsible for LKB1 protein stability.
机译:背景技术神经元极化是大脑发育过程中形态发生和连通性的重要步骤。丝氨酸/苏氨酸激酶LKB1是细胞极性,代谢,肿瘤发生的关键调节剂,是轴突形成所必需的。它由两种相关的且进化上保守的伪激酶,即STe20相关的ADapters(STRAD)α和β进行变构调节。 STRADα和STRADβ在发育中的神经系统中的作用尚未完全定义,也不清楚它们是否具有独特的功能。结果我们发现STRADα是高度剪接的,并且似乎是原始的STRAD旁系同源物。我们报告每个STRAD是足够的轴突发生和促进发展中的皮质细胞存活。我们还揭示了LKB1和STRADα之间体内的相互蛋白质稳定关系,其中STRADα通过细胞质区室化专门维持LKB1蛋白水平。结论我们证明了STRADβ在轴突发生中的新作用,并且还首次在体内证明了STRADα而非LRAD1负责LKB1蛋白的稳定性。

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