Brokaw C J
Division of Biology, California Institute of Technology, Pasadena.
Cell Motil Cytoskeleton. 1994;28(3):199-204. doi: 10.1002/cm.970280303.
Observations that were interpreted to provide evidence for equivalent functions of all axonemal dyneins should be reinterpreted, and models based on this assumption should be abandoned. In the future, attempts to understand the mechanisms for flagellar bending, oscillation, and bend propagation should start from the assumption that each type of axonemal dynein may have a specific function. At least three distinct functions can now be identified: bend initiation, maintenance of the angle of propagating bends, and generation of power to overcome viscous resistances. Only the last of these three functions is an outer arm dynein function.
那些被解释为提供所有轴丝动力蛋白功能等效证据的观察结果应重新解释,基于此假设的模型也应摒弃。未来,试图理解鞭毛弯曲、摆动和弯曲传播机制的研究应从这样一个假设出发,即每种类型的轴丝动力蛋白可能都有特定功能。目前至少可确定三种不同功能:弯曲起始、传播性弯曲角度的维持以及产生克服粘性阻力的动力。这三种功能中只有最后一种是外臂动力蛋白的功能。