Weasner Brandon P, Anderson Jason, Kumar Justin P
Department of Biology,Indiana University1001 E. 3rd StreetBloomington, IN 47401.
Proc Indian Natl Sci Acad B Biol Sci. 2004;B70(5-6):517-530.
One of the most exciting revelations in retinal biology is the realization that the molecules and mechanisms that regulate eye development have been conserved in all seeing animals including such diverse organisms as the fruit fly, mouse and man. The emerging commonality among mechanisms used in eye development allows for the use of model systems such as the fruit fly, Drosophila melanogaster, to provide key insights into the development and diseases of the mammalian eye. Eye specification in Drosophila is controlled, in part, by the concerted activities of eight nuclear proteins and several signal transduction cascades that together form a tightly woven regulatory network. Loss of function mutations in several components lead to the complete derailment of eye development while ectopic expression of threse genes in non-retinal tissues can direct the fates of these tissues towards eye formation. Here we will describe what is currently known about this remarkable regulatory cassettee highlight some of the outstanding questions that still need to be answered.
视网膜生物学中最令人兴奋的发现之一是,人们认识到调节眼睛发育的分子和机制在所有视觉动物中都是保守的,这些动物包括果蝇、小鼠和人类等多种生物。眼睛发育所使用的机制中出现的共性使得能够利用果蝇等模型系统来深入了解哺乳动物眼睛的发育和疾病。果蝇的眼睛特化部分受八种核蛋白的协同作用以及几个信号转导级联反应的控制,这些共同构成了一个紧密交织的调控网络。几个组件中的功能丧失突变会导致眼睛发育完全脱轨,而这些基因在非视网膜组织中的异位表达可以将这些组织的命运导向眼睛形成。在这里,我们将描述目前对这个非凡的调控盒的了解,并突出一些仍有待解答的重要问题。