Deutsch W A
Department of Biochemistry, Louisiana State University, Baton Rouge 70803, USA.
Insect Mol Biol. 1995 Feb;4(1):1-5. doi: 10.1111/j.1365-2583.1995.tb00001.x.
Although uracil-DNA glycosylases were at one time considered to be ubiquitous in nature, this DNA repair activity is notably absent in Drosophila melanogaster and other pupating insects. On the other hand, a nuclease has been identified in Drosophila that is specific for uracil-containing DNA, but curiously the expression of this activity is restricted to late larval stages of development. Since the nuclease activity is only detected near the time of histolysation, we began questioning the possible role uracil might play in the events associated with the eventual DNA degradation that is involved in the metamorphotic process. The results of these studies have provided us with a molecular model for pupating insects that contains all the necessary elements to program cells for their ultimate death, and in so doing, shows why uracil-DNA glycosylases would be incompatible with our proposed pathway for apoptosis.
虽然尿嘧啶-DNA糖基化酶曾一度被认为在自然界中普遍存在,但这种DNA修复活性在黑腹果蝇和其他化蛹昆虫中明显缺失。另一方面,在果蝇中已鉴定出一种对含尿嘧啶DNA具有特异性的核酸酶,但奇怪的是,这种活性的表达仅限于发育的幼虫后期阶段。由于核酸酶活性仅在组织溶解时被检测到,我们开始质疑尿嘧啶在与变态过程中最终DNA降解相关事件中可能发挥的作用。这些研究结果为化蛹昆虫提供了一个分子模型,该模型包含了将细胞编程使其最终死亡所需的所有必要元素,并且这样做表明了为什么尿嘧啶-DNA糖基化酶与我们提出的细胞凋亡途径不相容。