Rezaul Karim, Gupta Dipika, Semenova Irina, Ikeda Kazuho, Kraikivski Pavel, Yu Ji, Cowan Ann, Zaliapin Ilya, Rodionov Vladimir
R.D.Berlin Center for Cell Analysis and Modeling, and Department of Cell Biology, UConn Health, 400 Farmington Avenue, Farmington, CT 06030-6406, USA.
Current address: Quantitative Biology Center, RIKEN, Osaka 565-0874, Japan.
Traffic. 2016 May;17(5):475-86. doi: 10.1111/tra.12385. Epub 2016 Mar 28.
Bidirectional transport of membrane organelles along microtubules (MTs) is driven by plus-end directed kinesins and minus-end directed dynein bound to the same cargo. Activities of opposing MT motors produce bidirectional movement of membrane organelles and cytoplasmic particles along MT transport tracks. Directionality of MT-based transport might be controlled by a protein complex that determines which motor type is active at any given moment of time, or determined by the outcome of a tug-of-war between MT motors dragging cargo organelles in opposite directions. However, evidence in support of each mechanisms of regulation is based mostly on the results of theoretical analyses or indirect experimental data. Here, we test whether the direction of movement of membrane organelles in vivo can be controlled by the tug-of-war between opposing MT motors alone, by attaching a large number of kinesin-1 motors to organelles transported by dynein to minus-ends of MTs. We find that recruitment of kinesin significantly reduces the length and velocity of minus-end-directed dynein-dependent MT runs, leading to a reversal of the overall direction of dynein-driven organelles in vivo. Therefore, in the absence of external regulators tug-of-war between opposing MT motors alone is sufficient to determine the directionality of MT transport in vivo.
膜性细胞器沿微管(MTs)的双向运输由结合在同一货物上的正端定向驱动蛋白和负端定向动力蛋白驱动。相反方向的微管马达活动促使膜性细胞器和细胞质颗粒沿微管运输轨道进行双向移动。基于微管的运输方向性可能由一个蛋白质复合体控制,该复合体决定在任何给定时刻哪种马达类型处于活跃状态,或者由微管马达向相反方向拖动货物细胞器时的拔河结果决定。然而,支持每种调节机制的证据大多基于理论分析结果或间接实验数据。在这里,我们通过将大量驱动蛋白-1马达附着到由动力蛋白向微管负端运输的细胞器上,来测试体内膜性细胞器的移动方向是否仅能由相反方向的微管马达之间的拔河来控制。我们发现,驱动蛋白的募集显著降低了依赖负端定向动力蛋白的微管运行的长度和速度,导致动力蛋白驱动的细胞器在体内的整体移动方向发生逆转。因此,在没有外部调节因子的情况下,仅相反方向的微管马达之间的拔河就足以决定体内微管运输的方向性。