Lee Yuh-Ru Julie, Li Yan, Liu Bo
Section of Plant Biology, University of California, Davis, California 95616, USA.
Plant Cell. 2007 Aug;19(8):2595-605. doi: 10.1105/tpc.107.050716. Epub 2007 Aug 24.
In plant cells, cytokinesis is brought about by the phragmoplast. The phragmoplast has a dynamic microtubule array of two mirrored sets of microtubules, which are aligned perpendicularly to the division plane with their plus ends located at the division site. It is not well understood how the phragmoplast microtubule array is organized. In Arabidopsis thaliana, two homologous microtubule motor kinesins, PAKRP1/Kinesin-12A and PAKRP1L/Kinesin-12B, localize exclusively at the juxtaposing plus ends of the antiparallel microtubules in the middle region of the phragmoplast. When either kinesin was knocked out by T-DNA insertions, mutant plants did not show a noticeable defect. However, in the absence of both kinesins, postmeiotic development of the male gametophyte was severely inhibited. In dividing microspores of the double mutant, microtubules often became disorganized following chromatid segregation and failed to form an antiparallel microtubule array between reforming nuclei. Consequently, the first postmeiotic cytokinesis was abolished without the formation of a cell plate, which led to failures in the birth of the generative cell and, subsequently, the sperm. Thus, our results indicate that Kinesin-12A and Kinesin-12B jointly play a critical role in the organization of phragmoplast microtubules during cytokinesis in the microspore that is essential for cell plate formation. Furthermore, we conclude that Kinesin-12 members serve as dynamic linkers of the plus ends of antiparallel microtubules in the phragmoplast.
在植物细胞中,胞质分裂是由成膜体完成的。成膜体有两组镜像微管组成的动态微管阵列,它们垂直于分裂平面排列,其正端位于分裂位点。目前对于成膜体微管阵列是如何组织的还不太清楚。在拟南芥中,两种同源微管运动驱动蛋白,PAKRP1/驱动蛋白-12A和PAKRP1L/驱动蛋白-12B,仅定位在成膜体中间区域反平行微管并列的正端。当通过T-DNA插入敲除任何一种驱动蛋白时,突变植株并未表现出明显的缺陷。然而,在两种驱动蛋白都缺失的情况下,雄配子体的减数分裂后发育受到严重抑制。在双突变体的分裂小孢子中,微管在染色单体分离后常常变得紊乱,并且在重新形成的细胞核之间无法形成反平行微管阵列。因此,第一次减数分裂后胞质分裂被废除,没有形成细胞板,这导致生殖细胞以及随后精子的产生失败。因此,我们的结果表明,驱动蛋白-12A和驱动蛋白-12B在小孢子胞质分裂过程中成膜体微管的组织中共同发挥关键作用,这对于细胞板形成至关重要。此外,我们得出结论,驱动蛋白-12成员作为成膜体中反平行微管正端的动态连接物。