Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California; Bioinformatics Graduate Group, University of California, San Francisco, San Francisco, California.
Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California.
Biophys J. 2018 Feb 6;114(3):663-674. doi: 10.1016/j.bpj.2017.11.3784.
An important question in cell biology is whether cells are able to measure size, either whole cell size or organelle size. Perhaps cells have an internal chemical representation of size that can be used to precisely regulate growth, or perhaps size is just an accident that emerges due to constraint of nutrients. The eukaryotic flagellum is an ideal model for studying size sensing and control because its linear geometry makes it essentially one-dimensional, greatly simplifying mathematical modeling. The assembly of flagella is regulated by intraflagellar transport (IFT), in which kinesin motors carry cargo adaptors for flagellar proteins along the flagellum and then deposit them at the tip, lengthening the flagellum. The rate at which IFT motors are recruited to begin transport into the flagellum is anticorrelated with the flagellar length, implying some kind of communication between the base and the tip and possibly indicating that cells contain some mechanism for measuring flagellar length. Although it is possible to imagine many complex scenarios in which additional signaling molecules sense length and carry feedback signals to the cell body to control IFT, might the already-known components of the IFT system be sufficient to allow length dependence of IFT? Here we investigate a model in which the anterograde kinesin motors unbind after cargo delivery, diffuse back to the base, and are subsequently reused to power entry of new IFT trains into the flagellum. By mathematically modeling and simulating such a system, we are able to show that the diffusion time of the motors can in principle be sufficient to serve as a proxy for length measurement. We found that the diffusion model can not only achieve a stable steady-state length without the addition of any other signaling molecules or pathways, but also is able to produce the anticorrelation between length and IFT recruitment rate that has been observed in quantitative imaging studies.
细胞生物学中的一个重要问题是细胞是否能够测量大小,无论是整个细胞大小还是细胞器大小。也许细胞内部有一种化学物质可以代表大小,用于精确调节生长,或者大小只是由于营养物质的限制而产生的偶然现象。真核鞭毛是研究大小感应和控制的理想模型,因为它的线性几何形状使其基本上是一维的,极大地简化了数学建模。鞭毛的组装受到鞭毛内运输 (IFT) 的调节,其中驱动蛋白马达沿着鞭毛携带鞭毛蛋白的货物衔接器,然后将它们沉积在尖端,从而使鞭毛伸长。IFT 马达被招募开始向鞭毛运输的速度与鞭毛长度呈反相关,这表明基部和尖端之间存在某种通讯,并且细胞可能包含某种测量鞭毛长度的机制。尽管可以想象许多复杂的情况,其中额外的信号分子可以感知长度并将反馈信号传递到细胞体以控制 IFT,但 IFT 系统的已知组件是否足以允许 IFT 依赖于长度?在这里,我们研究了一种模型,其中顺行驱动蛋白马达在货物传递后解联,扩散回基部,随后被重新用于为新的 IFT 列车进入鞭毛提供动力。通过对该系统进行数学建模和模拟,我们能够表明马达的扩散时间原则上可以作为长度测量的代理。我们发现,扩散模型不仅可以在不添加任何其他信号分子或途径的情况下实现稳定的稳态长度,而且还能够产生定量成像研究中观察到的长度与 IFT 招募率之间的反相关关系。