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Expression of the Mitotic Motor Protein Eg5 in Postmitotic Neurons: Implications for Neuronal Development

机译:有丝分裂运动蛋白Eg5在有丝分裂后神经元中的表达:对神经元发育的影响。

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摘要

It is well established that the microtubules of the mitotic spindle are organized by a variety of motor proteins, and it appears that the same motors or closely related variants organize microtubules in the postmitotic neuron. Specifically, cytoplasmic dynein and the kinesin-related motor known as CHO1/MKLP1 are used within the mitotic spindle, and recent studies suggest that they are also essential for the establishment of the axonal and dendritic microtubule arrays of the neuron. Other motors are required to tightly regulate microtubule behaviors in the mitotic spindle, and it is attractive to speculate that these motors might also help to regulate microtubule behaviors in the neuron. Here we show that a homolog of the mitotic kinesin-related motor known as Eg5 continues to be expressed in rodent neurons well after their terminal mitotic division. In neurons, Eg5 is directly associated with the microtubule array and is enriched within the distal regions of developing processes. This distal enrichment is transient, and typically lost after a process has been clearly defined as an axon or a dendrite. Strong expression can resume later in development, and if so, the protein concentrates within newly forming sprouts at the distal tips of dendrites. We suggest that Eg5 generates forces that help to regulate microtubule behaviors within the distal tips of developing axons and dendrites.
机译:公认的是,有丝分裂纺锤体的微管由多种运动蛋白组成,并且似乎相同的运动或密切相关的变异体在有丝分裂后的神经元中组织了微管。具体而言,在有丝分裂纺锤体中使用了细胞质动力蛋白和与驱动蛋白有关的运动,称为CHO1 / MKLP1,最近的研究表明,它们对于建立神经元的轴突和树突微管阵列也至关重要。还需要其他马达来严格调节有丝分裂纺锤体中的微管行为,并且引人注目的是,这些马达也可能有助于调节神经元中的微管行为。在这里,我们显示出与有丝分裂驱动蛋白相关的运动(称为Eg5)的同源物在啮齿动物神经元的末次有丝分裂分裂后仍继续表达。在神经元中,Eg5与微管阵列直接相关,并在发育过程的远端区域富集。这种远端富集是短暂的,通常在明确定义为轴突或树突后消失。强表达可以在发育后期恢复,如果是这样,则蛋白质会集中在树突末端的新形成的芽中。我们建议,Eg5产生的力有助于调节发育中的轴突和树突的远端尖端内的微管行为。

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