Tubman Emily, He Yungui, Hays Thomas S, Odde David J
Department of Biomedical Engineering, University of Minnesota, Minneapolis, MN 55455 USA.
Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455 USA.
Cell Mol Bioeng. 2018 Feb;11(1):25-36. doi: 10.1007/s12195-017-0500-0. Epub 2017 Aug 21.
The microtubule motor protein kinesin-5 is well known to establish the bipolar spindle by outward sliding of antiparallel interpolar microtubules. In yeast, kinesin-5 also facilitates chromosome alignment "congression" at the spindle equator by preferentially depolymerizing long kinetochore microtubules (kMTs). The motor protein kinesin-8 has also been linked to chromosome congression. Therefore, we sought to determine whether kinesin-5 or kinesin-8 facilitates chromosome congression in insect spindles.
RNAi of the kinesin-5 Klp61F and kinesin-8 Klp67A were performed separately in S2 cells to test for inhibited chromosome congression. Klp61F RNAi, Klp67A RNAi, and control metaphase mitotic spindles expressing fluorescent tubulin and fluorescent Cid were imaged, and their fluorescence distributions were compared.
RNAi of Klp61F with a weak Klp61F knockdown resulted in longer kMTs and less congressed kinetochores compared to control over a range of conditions, consistent with kinesin-5 length-dependent depolymerase activity. RNAi of the kinesin-8 Klp67A revealed that kMTs relative to the spindle lengths were not longer compared to control, but rather that the spindles were longer, indicating that Klp67A acts preferentially as a length-dependent depolymerase on interpolar microtubules without significantly affecting kMT length and chromosome congression.
This study demonstrates that in addition to establishing the bipolar spindle, kinesin-5 regulates kMT length to facilitate chromosome congression in insect spindles. It expands on previous yeast studies, and it expands the role of kinesin-5 to include kMT assembly regulation in eukaryotic mitosis.
微管运动蛋白驱动蛋白-5因通过反向平行的极间微管向外滑动来建立双极纺锤体而广为人知。在酵母中,驱动蛋白-5还通过优先解聚长的动粒微管(kMTs)来促进染色体在纺锤体赤道面的排列“汇聚”。运动蛋白驱动蛋白-8也与染色体汇聚有关。因此,我们试图确定驱动蛋白-5或驱动蛋白-8是否促进昆虫纺锤体中的染色体汇聚。
在S2细胞中分别对驱动蛋白-5 Klp61F和驱动蛋白-8 Klp67A进行RNA干扰,以测试染色体汇聚是否受到抑制。对表达荧光微管蛋白和荧光Cid的Klp61F RNA干扰、Klp67A RNA干扰和对照中期有丝分裂纺锤体进行成像,并比较它们的荧光分布。
与对照相比,在一系列条件下,使用弱敲低的Klp61F进行RNA干扰导致kMTs更长,动粒汇聚更少,这与驱动蛋白-5的长度依赖性解聚酶活性一致。驱动蛋白-8 Klp67A的RNA干扰显示,相对于纺锤体长度,kMTs并不比对照长,而是纺锤体更长,这表明Klp67A优先作为极间微管上的长度依赖性解聚酶起作用,而不会显著影响kMT长度和染色体汇聚。
本研究表明,除了建立双极纺锤体外,驱动蛋白-5还调节kMT长度以促进昆虫纺锤体中的染色体汇聚。它扩展了先前的酵母研究,并将驱动蛋白-5的作用扩展到包括真核有丝分裂中kMT组装的调节。