Welz Tobias, Kerkhoff Eugen
a University Hospital Regensburg, Department of Neurology , Molecular Cell Biology Laboratory , Regensburg , Germany.
Small GTPases. 2019 Mar;10(2):111-121. doi: 10.1080/21541248.2017.1281863. Epub 2017 Apr 10.
Spir actin nucleators and myosin V motor proteins were recently discovered to coexist in a protein complex. The direct interaction allows the coordinated activation of actin motor proteins and actin filament track generation at vesicle membranes. By now the cooperation of myosin V (MyoV) motors and Spir actin nucleation function has only been shown in the exocytic transport of Rab11 vesicles in metaphase mouse oocytes. Next to Rab11, myosin V motors however interact with a variety of Rab GTPases including Rab3, Rab8 and Rab10. As a common theme most of the MyoV interacting Rab GTPases function at different steps along the exocytic transport routes. We here summarize the different transport functions of class V myosins and provide as proof of principle data showing a colocalization of Spir actin nucleators and MyoVa at Rab8a vesicles. This suggests that besides Rab11/MyoV transport also the Rab8/MyoV and possibly other MyoV transport processes recruit Spir actin filament nucleation function.
螺旋肌动蛋白成核因子和肌球蛋白V运动蛋白最近被发现共存于一个蛋白质复合物中。这种直接相互作用使得肌动蛋白运动蛋白的协同激活以及囊泡膜上肌动蛋白丝轨道的生成成为可能。到目前为止,肌球蛋白V(MyoV)运动蛋白与螺旋肌动蛋白成核功能的协同作用仅在中期小鼠卵母细胞中Rab11囊泡的胞吐运输中得到证实。然而,除了Rab11之外,肌球蛋白V运动蛋白还与多种Rab GTP酶相互作用,包括Rab3、Rab8和Rab10。作为一个共同特点,大多数与MyoV相互作用的Rab GTP酶在胞吐运输途径的不同步骤发挥作用。我们在此总结了V类肌球蛋白的不同运输功能,并提供了原理性数据证明螺旋肌动蛋白成核因子和MyoVa在Rab8a囊泡处共定位。这表明除了Rab11/MyoV运输外,Rab8/MyoV以及可能的其他MyoV运输过程也招募螺旋肌动蛋白丝成核功能。