Department of Chemical and Biological Engineering and Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA.
Chaos. 2013 Jun;23(2):025105. doi: 10.1063/1.4808157.
Terminal regions of the Drosophila embryo are patterned by the localized activation of Mitogen Activated Protein Kinase (MAPK), which induces zygotic genes through relief of their repression by transcriptional repressor Capicua. The levels of MAPK activation at the anterior and posterior termini are close to each other, but the expression patterns of MAPK-target genes, such as zerknüllt (zen) and tailless (tll), display strong anterior-posterior (AP) asymmetry. This region-specific response to MAPK activation provides a clear example of context-dependent interpretation of inductive signaling, a common developmental effect that remains poorly understood. In the past, the AP asymmetry of zen expression was attributed to a mechanism that depends on MAPK substrate competition. We present data suggesting that the asymmetric expression of tll is generated by a different mechanism, based on feedforward control and multiple enhancers of the tll gene. A simple mathematical model of this mechanism correctly predicts how the wild-type expression pattern of tll changes in mutants affecting the anterior, dorsoventral, and terminal patterning systems and some of their direct targets.
果蝇胚胎的末端区域是通过有丝分裂原激活蛋白激酶(MAPK)的局部激活来模式化的,MAPK 通过解除转录抑制因子 Capicua 对合子基因的抑制来诱导合子基因。在前、后末端处的 MAPK 激活水平彼此接近,但 MAPK 靶基因(如 zerknüllt (zen) 和 tailless (tll))的表达模式显示出强烈的前后(AP)不对称性。这种对 MAPK 激活的区域特异性反应提供了一个明确的例子,说明了诱导信号的上下文相关解释,这是一种常见的发育效应,但仍知之甚少。过去,zen 表达的 AP 不对称性归因于一种依赖于 MAPK 底物竞争的机制。我们提供的数据表明,tll 的不对称表达是由一种不同的机制产生的,该机制基于前馈控制和 tll 基因的多个增强子。该机制的一个简单数学模型正确地预测了影响前、背腹和末端模式系统及其一些直接靶标的突变体如何改变 tll 的野生型表达模式。