Ismael Amber, Stone David E
Department of Cell and Developmental Biology, University of Colorado, Denver Anschutz Medical Campus, Aurora, CO, USA.
Department of Biological Sciences, University of Illinois at Chicago, Chicago, IL, USA.
Cell Logist. 2017 Apr 11;7(2):e1314237. doi: 10.1080/21592799.2017.1314237. eCollection 2017.
The ability of cells to direct their movement and growth in response to shallow chemical gradients is essential in the life cycles of all eukaryotic organisms. The signaling mechanisms underlying directional sensing in chemotactic cells have been well studied; however, relatively little is known about how chemotropic cells interpret chemical gradients. Recent studies of chemotropism in budding and fission yeast have revealed 2 quite different mechanisms-biased wandering of the polarity complex, and differential internalization of the receptor and G protein. Each of these mechanisms has been proposed to play a key role in decoding mating pheromone gradients. Here we explore how they may work together as 2 essential components of one gradient sensing machine.
细胞响应浅化学梯度来指导自身运动和生长的能力在所有真核生物的生命周期中至关重要。趋化细胞中定向感知的信号传导机制已得到充分研究;然而,关于向化细胞如何解读化学梯度却知之甚少。最近对芽殖酵母和裂殖酵母向化作用的研究揭示了两种截然不同的机制——极性复合体的偏向性游动,以及受体和G蛋白的差异内化。有人提出这些机制中的每一种在解码交配信息素梯度中都起着关键作用。在这里,我们探讨它们如何作为一个梯度传感机器的两个重要组成部分协同工作。