Fulton C, Walsh C
J Cell Biol. 1980 May;85(2):346-60. doi: 10.1083/jcb.85.2.346.
This paper presents evidence that the phenotypic transformation of Naegleria gruberi from amebae to flagellates that occurs when cells are placed in a nutrient-free aqueous environment is dependent on transcription and translation. RNA and protein are synthesized during the hour-long differentiation. Actinomycin D and daunomycin selectively inhibit RNA synthesis, and cycloheximide selectively inhibits protein synthesis, throughout the time required for differentiation. These inhibitors prevent differentiation if added soon after the cells are transferred to nonnutrient buffer but cease to block specific differentiation events at subsequent, reproducible times, the transition points. After each transition point, morphogenesis can occur in the presence of the inhibitor and in the virtual absence of transcription or translation. A map of the transition points indicates that RNA synthesis is required until halfway through the temporal process from initiation to flagellum assembly, and that protein synthesis is required until three-fourths of the way through. Even when flagellum outgrowth can occur in the presence of cycloheximide, the length of the flagella formed is determined by the extent of synthesis of an unknown "limiting precursor." The transition points for formation of flagella and for formation of the streamlined flagellate body shape are temporally separate. These results indicate that differentiation in Naegleria involves a redirection of cell metabolism to produce new RNA and protein molecules that are essential for morphogenesis.
本文提供了证据表明,当细胞置于无营养的水环境中时,格氏耐格里变形虫从阿米巴转变为鞭毛虫的表型转化依赖于转录和翻译。在长达一小时的分化过程中会合成RNA和蛋白质。放线菌素D和柔红霉素在整个分化所需时间内选择性抑制RNA合成,环己酰亚胺选择性抑制蛋白质合成。如果在细胞转移到无营养缓冲液后不久添加这些抑制剂,会阻止分化,但在随后可重复的时间点(转变点),它们会停止阻断特定的分化事件。在每个转变点之后,形态发生可以在抑制剂存在且几乎没有转录或翻译的情况下发生。转变点图谱表明,从起始到鞭毛组装的时间过程进行到一半之前都需要RNA合成,而蛋白质合成则需要进行到四分之三的时间。即使在环己酰亚胺存在的情况下鞭毛可以长出,所形成鞭毛的长度也由一种未知的“限制性前体”的合成程度决定。鞭毛形成和流线型鞭毛虫体型形成的转变点在时间上是分开的。这些结果表明,耐格里变形虫的分化涉及细胞代谢的重新定向,以产生对形态发生至关重要的新RNA和蛋白质分子。