Oh Doogie, Yu Che-Hang, Needleman Daniel J
John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138; Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138; Faculty of Arts and Sciences Center for Systems Biology, Harvard University, Cambridge, MA 02138
John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138;
Proc Natl Acad Sci U S A. 2016 Aug 2;113(31):8729-34. doi: 10.1073/pnas.1607498113. Epub 2016 Jul 20.
Concentration gradients of soluble proteins are believed to be responsible for control of morphogenesis of subcellular systems, but the mechanisms that generate the spatial organization of these subcellular gradients remain poorly understood. Here, we use a newly developed multipoint fluorescence fluctuation spectroscopy technique to study the ras-related nuclear protein (Ran) pathway, which forms soluble gradients around chromosomes in mitosis and is thought to spatially regulate microtubule behaviors during spindle assembly. We found that the distribution of components of the Ran pathway that influence microtubule behaviors is determined by their interactions with microtubules, resulting in microtubule nucleators being localized by the microtubules whose formation they stimulate. Modeling and perturbation experiments show that this feedback makes the length of the spindle insensitive to the length scale of the Ran gradient, allows the spindle to assemble outside the peak of the Ran gradient, and explains the scaling of the spindle with cell size. Such feedback between soluble signaling pathways and the mechanics of the cytoskeleton may be a general feature of subcellular organization.
可溶性蛋白质的浓度梯度被认为是负责亚细胞系统形态发生的控制,但产生这些亚细胞梯度空间组织的机制仍知之甚少。在这里,我们使用一种新开发的多点荧光涨落光谱技术来研究Ras相关核蛋白(Ran)途径,该途径在有丝分裂过程中围绕染色体形成可溶性梯度,并被认为在纺锤体组装过程中对微管行为进行空间调节。我们发现,影响微管行为的Ran途径成分的分布是由它们与微管的相互作用决定的,导致微管成核剂被它们所刺激形成的微管所定位。建模和扰动实验表明,这种反馈使纺锤体的长度对Ran梯度的长度尺度不敏感,允许纺锤体在Ran梯度峰值之外组装,并解释了纺锤体与细胞大小的比例关系。可溶性信号通路与细胞骨架力学之间的这种反馈可能是亚细胞组织的一个普遍特征。