Cibert Christian
Groupe de Morphométrie et de Modélisation Cellulaire, Département de Biologie du Développement, Institut Jacques Monod, CNRS, Universités Paris 6 and Paris 7, Paris, France.
Cell Motil Cytoskeleton. 2003 Apr;54(4):296-316. doi: 10.1002/cm.10100.
Radial spokes and the consequences of their relationships with the central apparatus seem to play a very important role in the regulation of axonemal activity. We modeled their behavior and observed that it appears to differ in the cilium and the flagellum with respect to the development of bending as a function of time. Specifically, our calculation raises the question of the real function of the radial spokes in the regulation of the axoneme, because a given curvature of the flagellar axoneme may correspond to two opposite of their tilts. The stable nil/low amplitude shear points that we had characterized along the flagellum allowed us to describe their axoneme as a series of modules [Cibert, 2002: Cell Motil. Cytoskeleton 51:89-111]. We observed that a nil/low shearing point moves along each module during beating when a new bend is created at the base of the flagellum [Cibert, 2001: Cell Motil. Cytoskeleton 49:161-175]. We propose that the structural gradients of isoforms of tubulin could be basic verniers that act as structural references for the axonemal machinery during the beating. This allowed us to interpret the axonemal organization as a segmented structure, that could be analyzed according to the complexion(1) theory and Shannon's information theory, which associate entropy and probability in the creation of information. The important consequence of this interpretation is that regulation of the axonemal machinery appears to be due to the upstream and downstream cross-talk between the axonemal segments that do not involve any dedicated integrative structure but depend on the energy level of the entire length of each module.
辐条及其与中心装置的关系所产生的影响似乎在轴丝活动的调节中起着非常重要的作用。我们对它们的行为进行了建模,并观察到在纤毛和鞭毛中,随着时间推移弯曲的发展情况似乎有所不同。具体而言,我们的计算提出了辐条在轴丝调节中的实际功能问题,因为鞭毛轴丝的给定曲率可能对应于它们两种相反的倾斜状态。我们在鞭毛上确定的稳定的零/低振幅剪切点,使我们能够将其轴丝描述为一系列模块[西伯特,2002年:《细胞运动与细胞骨架》51卷:89 - 111页]。我们观察到,当在鞭毛基部产生新的弯曲时,零/低剪切点在每次摆动过程中会沿着每个模块移动[西伯特,2001年:《细胞运动与细胞骨架》49卷:161 - 175页]。我们提出,微管蛋白同工型的结构梯度可能是基本的微调装置,在摆动过程中作为轴丝机制的结构参考。这使我们能够将轴丝组织解释为一种分段结构,可以根据复杂性理论和香农信息论进行分析,这两种理论在信息产生过程中关联了熵和概率。这种解释的重要结果是,轴丝机制的调节似乎是由于轴丝各段之间的上下游相互作用,这种相互作用不涉及任何专门的整合结构,而是取决于每个模块全长的能量水平。