Molecular and Cellular Biology Program, University of Washington, Box 355065, Seattle, WA 98195-5065, USA.
Development. 2009 Dec;136(24):4187-97. doi: 10.1242/dev.042770.
Organ morphogenesis requires cooperation between cells, which determine their course of action based upon location within a tissue. Just as important, cells must synchronize their activities, which requires awareness of developmental time. To understand how cells coordinate behaviors in time and space, we analyzed Drosophila egg chamber development. We found that the transcription factor Tramtrack69 (TTK69) controls the fates and shapes of all columnar follicle cells by integrating temporal and spatial information, restricting characteristic changes in morphology and expression that occur at stage 10B to appropriate domains. TTK69 is required again later in oogenesis: it controls the volume of the dorsal-appendage (DA) tubes by promoting apical re-expansion and lateral shortening of DA-forming follicle cells. We show that TTK69 and Notch compete to repress each other's expression and that a local Ecdysone signal is required to shift the balance in favor of TTK69. We hypothesize that TTK69 then cooperates with spatially restricted co-factors to define appropriate responses to a globally available (but as yet unidentified) temporal signal that initiates the S10B transformations.
器官形态发生需要细胞之间的合作,细胞根据其在组织中的位置来决定其行动方向。同样重要的是,细胞必须协调它们的活动,这需要了解发育时间。为了了解细胞如何在时间和空间上协调行为,我们分析了果蝇卵室的发育。我们发现,转录因子 Tramtrack69(TTK69)通过整合时间和空间信息来控制所有柱状滤泡细胞的命运和形状,将在 10B 期发生的特征性形态和表达变化限制在适当的区域。TTK69 在卵母细胞发生的后期再次被需要:它通过促进形成 DA 的滤泡细胞的顶端重新扩张和侧向缩短来控制背附肢(DA)管的体积。我们表明,TTK69 和 Notch 竞争以相互抑制对方的表达,并且需要局部的蜕皮激素信号来使平衡有利于 TTK69。我们假设 TTK69 然后与空间上受限的共因子合作,以响应全局可用(但尚未鉴定)的时间信号,该信号启动 S10B 转化。