School of Applied Biosciences, Kyungpook National University, Daegu, 702-701, Republic of Korea.
Plant Reprod. 2014 Mar;27(1):7-17. doi: 10.1007/s00497-013-0235-6. Epub 2013 Oct 22.
Arabidopsis Fused kinase TWO-IN-ONE (TIO) controls phragmoplast expansion through its interaction with the Kinesin-12 subfamily proteins that anchor the plus ends of interdigitating microtubules in the phragmoplast midzone. Previous analyses of loss-of-function mutants and RNA interference lines revealed that TIO positively controls both somatic and gametophytic cell cytokinesis; however, knowledge of the full spectrum of TIO functions during plant development remains incomplete. To characterize TIO functions further, we expressed TIO and a range of TIO variants under control of the TIO promoter in wild-type Arabidopsis plants. We discovered that TIO-overexpressing transgenic lines produce enlarged pollen grains, arising from incomplete cytokinesis during male meiosis, and show sporophytic abnormalities indicative of polyploidy. These phenotypes arose independently in TIO variants in which either gametophytic function or the ability of TIO to interact with Kinesin-12 subfamily proteins was abolished. Interaction assays in yeast showed TIO to bind to the AtNACK2/TETRASPORE, and plants doubly homozygous for kinesin-12a and kinesin-12b knockout mutations to produce enlarged pollen grains. Our results show TIO to dominantly inhibit male meiotic cytokinesis in a dosage-dependent manner that may involve direct binding to a component of the canonical NACK-PQR cytokinesis signaling pathway.
拟南芥融合激酶 TWO-IN-ONE(TIO)通过与其锚定在胞质分裂中期的交错微管的正极的 Kinesin-12 亚家族蛋白相互作用来控制成膜体的扩展。对功能丧失突变体和 RNA 干扰系的分析表明,TIO 正向控制体细胞和配子体细胞胞质分裂;然而,对 TIO 在植物发育过程中的全部功能的了解仍然不完整。为了进一步表征 TIO 的功能,我们在野生型拟南芥植物中表达了 TIO 和一系列 TIO 变体,并受 TIO 启动子的控制。我们发现,TIO 过表达转基因系产生了增大的花粉粒,这是由于雄性减数分裂期间不完全的胞质分裂引起的,并且表现出多倍体的孢子体异常。这些表型在 TIO 变体中独立出现,这些变体要么丧失了配子体功能,要么丧失了 TIO 与 Kinesin-12 亚家族蛋白相互作用的能力。酵母中的相互作用测定表明,TIO 与 AtNACK2/TETRASPORE 结合,并且植物双重纯合缺失突变体 kinesin-12a 和 kinesin-12b 产生增大的花粉粒。我们的结果表明,TIO 以剂量依赖的方式显性抑制雄性减数分裂胞质分裂,这可能涉及与经典 NACK-PQR 胞质分裂信号通路的一个成分的直接结合。