Treisman Jessica E
Department of Cell Biology and Kimmel Center for Biology and Medicine of the Skirball Institute, NYU School of Medicine, New York, NY, USA.
Wiley Interdiscip Rev Dev Biol. 2013 Jul;2(4):545-57. doi: 10.1002/wdev.100. Epub 2012 Nov 16.
Drosophila eye development has been extensively studied, due to the ease of genetic screens for mutations disrupting this process. The eye imaginal disc is specified during embryonic and larval development by the Pax6 homolog Eyeless and a network of downstream transcription factors. Expression of these factors is regulated by signaling molecules and also indirectly by growth of the eye disc. Differentiation of photoreceptor clusters initiates in the third larval instar at the posterior of the eye disc and progresses anteriorly, driven by the secreted protein Hedgehog. Within each cluster, the combined activities of Hedgehog signaling and Notch-mediated lateral inhibition induce and refine the expression of the transcription factor Atonal, which specifies the founding R8 photoreceptor of each ommatidium. Seven additional photoreceptors, followed by cone and pigment cells, are successively recruited by the signaling molecules Spitz, Delta, and Bride of sevenless. Combinations of these signals and of intrinsic transcription factors give each ommatidial cell its specific identity. During the pupal stages, rhodopsins are expressed, and the photoreceptors and accessory cells take on their final positions and morphologies to form the adult retina. Over the past few decades, the genetic analysis of this small number of cell types arranged in a repetitive structure has allowed a remarkably detailed understanding of the basic mechanisms controlling cell differentiation and morphological rearrangement.
由于易于对破坏果蝇眼睛发育过程的突变进行遗传筛选,果蝇眼睛发育已得到广泛研究。眼成虫盘在胚胎和幼虫发育期间由Pax6同源物无眼蛋白及下游转录因子网络所确定。这些因子的表达受信号分子调控,也间接受眼成虫盘生长的调控。光感受器簇的分化在第三龄幼虫期于眼成虫盘后部开始,并在分泌蛋白刺猬索尼克的驱动下向前推进。在每个簇内,刺猬索尼克信号传导和Notch介导的侧向抑制的联合作用诱导并优化转录因子无调性的表达,该转录因子确定每个小眼的起始R8光感受器。信号分子Spitz、Delta和七无之新娘依次招募另外七个光感受器,随后是视锥细胞和色素细胞。这些信号与内在转录因子的组合赋予每个小眼细胞其特定身份。在蛹期,视紫红质表达,光感受器和辅助细胞占据其最终位置并形成其最终形态,以形成成年视网膜。在过去几十年中,对这种以重复结构排列的少数细胞类型的遗传分析,使得人们对控制细胞分化和形态重排的基本机制有了非常详细的了解。