Hale Rosalind, Brittle Amy L, Fisher Katherine H, Monk Nicholas A M, Strutt David
Bateson Centre, University of Sheffield, Sheffield, United Kingdom.
School of Mathematics and Statistics, University of Sheffield, Sheffield, United Kingdom.
Elife. 2015 Feb 24;4:e05789. doi: 10.7554/eLife.05789.
To understand how long-range patterning gradients are interpreted at the cellular level, we investigate how a gradient of expression of the Four-jointed kinase specifies planar polarised distributions of the cadherins Fat and Dachsous in the Drosophila wing. We use computational modelling to test different scenarios for how Four-jointed might act and test the model predictions by employing fluorescence recovery after photobleaching as an in vivo assay to measure the influence of Four-jointed on Fat-Dachsous binding. We demonstrate that in vivo, Four-jointed acts both on Fat to promote its binding to Dachsous and on Dachsous to inhibit its binding to Fat, with a bias towards a stronger effect on Fat. Overall, we show that opposing gradients of Fat and Dachsous phosphorylation are sufficient to explain the observed pattern of Fat-Dachsous binding and planar polarisation across the wing, and thus demonstrate the mechanism by which a long-range gradient is interpreted.
为了了解长程模式梯度在细胞水平上是如何被解读的,我们研究了四关节激酶的表达梯度如何在果蝇翅膀中指定钙黏蛋白Fat和Dachsous的平面极化分布。我们使用计算模型来测试四关节激酶可能发挥作用的不同情况,并通过采用光漂白后的荧光恢复作为体内测定方法来测试模型预测,以测量四关节激酶对Fat-Dachsous结合的影响。我们证明,在体内,四关节激酶既作用于Fat以促进其与Dachsous的结合,也作用于Dachsous以抑制其与Fat的结合,且对Fat的影响更强。总体而言,我们表明Fat和Dachsous磷酸化的相反梯度足以解释在翅膀上观察到的Fat-Dachsous结合模式和平面极化,从而证明了长程梯度被解读的机制。