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首页> 外文期刊>Molecular biology of the cell >The Caenorhabditis elegans Aurora B Kinase AIR-2 Phosphorylates and Is Required for the Localization of a BimC Kinesin to Meiotic and Mitotic Spindles
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The Caenorhabditis elegans Aurora B Kinase AIR-2 Phosphorylates and Is Required for the Localization of a BimC Kinesin to Meiotic and Mitotic Spindles

机译:秀丽隐杆线虫Aurora B激酶AIR-2磷酸化,是将BimC驱动蛋白定位于减数分裂和有丝分裂纺锤体所必需的

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BimC kinesins are required for mitotic spindle assembly in a variety of organisms. These proteins are localized to centrosomes, spindle microtubules, and the spindle midzone. We have previously shown that the Caenorhabditis elegans Aurora B kinase AIR-2 is required for the localization of the ZEN-4 kinesin protein to midzone microtubules. To determine whether the association of BimC kinesins with spindle microtubules is also dependent on AIR-2, we examined the expression pattern of BMK-1, a C. elegans BimC kinesin, in wild-type and AIR-2–deficient embryos. BMK-1 is highly expressed in the hermaphrodite gonad and is localized to meiotic spindle microtubules in the newly fertilized embryo. In mitotic embryos, BMK-1 is associated with spindle microtubules from prophase through anaphase and is concentrated at the spindle midzone during anaphase and telophase. In the absence of AIR-2, BMK-1 localization to meiotic and mitotic spindles is greatly reduced. This is not a consequence of loss of ZEN-4 localization because BMK-1 is appropriately localized in ZEN-4–deficient embryos. Furthermore, AIR-2 and BMK-1 directly interact with one another and the C-terminal tail domain of BMK-1 is specifically phosphorylated by AIR-2 in vitro. Together with our previous data, these results suggest that at least one function of the Aurora B kinases is to recruit spindle-associated motor proteins to their sites of action.
机译:BimC驱动蛋白是多种生物中有丝分裂纺锤体组装所必需的。这些蛋白质位于中心体,纺锤体微管和纺锤体中区。先前我们已经表明,秀丽隐杆线虫Aurora B激酶AIR-2是ZEN-4驱动蛋白定位于中区微管所必需的。为了确定BimC驱动蛋白与纺锤体微管的关联是否也依赖于AIR-2,我们检查了BMK-1(秀丽隐杆线虫BimC驱动蛋白)在野生型和AIR-2缺陷型胚胎中的表达模式。 BMK-1在雌雄同体性腺中高度表达,并定位于新受精胚胎中的减数分裂纺锤体微管中。在有丝分裂的胚胎中,BMK-1与从前期到后期的纺锤体微管有关,并在后期和末期集中在纺锤体中部。在没有AIR-2的情况下,BMK-1在减数分裂和有丝分裂纺锤体中的定位大大降低。这不是ZEN-4定位丢失的结果,因为BMK-1适当地定位在ZEN-4缺陷的胚胎中。此外,AIR-2和BMK-1彼此直接相互作用,并且BM-2的C末端尾部结构域在体外被AIR-2特异性磷酸化。与我们以前的数据一起,这些结果表明,Aurora B激酶的至少一种功能是将纺锤体相关的运动蛋白募集到它们的作用位点。

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