Tracking Shallow Chemical Gradients by Actin-Driven Wandering of the Polarization Site

被引:82
作者
Dyer, Jayme M. [1 ]
Savage, Natasha S. [1 ]
Jin, Meng [2 ]
Zyla, Trevin R. [1 ]
Elston, Timothy C. [3 ]
Lew, Daniel J. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[2] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
关键词
HETEROTRIMERIC G-PROTEIN; YEAST-CELL POLARITY; BUDDING YEAST; CHEMOTACTIC RESPONSE; MYOSIN V; ESTABLISHMENT; DYNAMICS; MORPHOGENESIS; MECHANISM; NETWORK;
D O I
10.1016/j.cub.2012.11.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Many cells are remarkably proficient at tracking very shallow chemical gradients, despite considerable noise from stochastic receptor-ligand interactions. Motile cells appear to undergo a biased random walk: spatial noise in receptor activity may determine the instantaneous direction, but because noise is spatially unbiased, it is filtered out by time averaging, resulting in net movement upgradient. How nonmotile cells might filter out noise is unknown. Results: Using yeast chemotropic mating as a model, we demonstrate that a polarized patch of polarity regulators "wanders" along the cortex during gradient tracking. Computational and experimental findings suggest that actin-directed membrane traffic contributes to wandering by diluting local polarity factors. The pheromone gradient appears to bias wandering via interactions between receptor-activated Gp gamma and polarity regulators. Artificially blocking patch wandering impairs gradient tracking. Conclusions: We suggest that the polarity patch undergoes an intracellular biased random walk that enables noise filtering by time averaging, allowing nonmotile cells to track shallow gradients.
引用
收藏
页码:32 / 41
页数:10
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