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Drosophila CLIP-190 and mammalian CLIP-170 display reduced microtubule plus end association in the nervous system

机译:果蝇CLIP-190和哺乳动物CLIP-170在神经系统中的微管加末端结合减少

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摘要

Axons act like cables, electrically wiring the nervous system. Polar bundles of microtubules (MTs) form their backbones and drive their growth. Plus end–tracking proteins (+TIPs) regulate MT growth dynamics and directionality at their plus ends. However, current knowledge about +TIP functions, mostly derived from work in vitro and in nonneuronal cells, may not necessarily apply to the very different context of axonal MTs. For example, the CLIP family of +TIPs are known MT polymerization promoters in nonneuronal cells. However, we show here that neither Drosophila CLIP-190 nor mammalian CLIP-170 is a prominent MT plus end tracker in neurons, which we propose is due to low plus end affinity of the CAP-Gly domain–containing N-terminus and intramolecular inhibition through the C-terminus. Instead, both CLIP-190 and CLIP-170 form F-actin–dependent patches in growth cones, mediated by binding of the coiled-coil domain to myosin-VI. Because our loss-of-function analyses in vivo and in culture failed to reveal axonal roles for CLIP-190, even in double-mutant combinations with four other +TIPs, we propose that CLIP-190 and -170 are not essential axon extension regulators. Our findings demonstrate that +TIP functions known from nonneuronal cells do not necessarily apply to the regulation of the very distinct MT networks in axons.
机译:轴突就像电缆一样,为神经系统供电。极性束微管(MT)形成其主干并驱动其生长。正末追踪蛋白(+ TIP)在正末调节MT的生长动力学和方向性。但是,有关+ TIP功能的当前知识(主要来自体外和非神经元细胞中的工作)可能不一定适用于轴突MT的非常不同的情况。例如,CLIP + TIP家族是非神经细胞中已知的MT聚合促进剂。但是,我们在这里表明,果蝇CLIP-190和哺乳动物CLIP-170都不是神经元中显着的MT加端追踪剂,我们提出这是由于含CAP-Gly结构域的N端的低加端亲和力和分子内抑制作用通过C端。相反,CLIP-190和CLIP-170都在生长锥中形成F-肌动蛋白依赖性斑块,由卷曲螺旋结构域与肌球蛋白VI的结合介导。因为我们在体内和文化中的功能丧失分析未能揭示CLIP-190的轴突作用,即使在与其他四个+ TIP的双突变组合中,我们也认为CLIP-190和-170不是必不可少的轴突延伸调节剂。我们的发现表明,非神经元细胞已知的+ TIP功能不一定适用于轴突中非常不同的MT网络的调节。

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