Shaw M K, Thompson J, Sinden R E
Molecular and Cellular Parasitology Group, Department of Biology, Imperial College of Science, Technology and Medicine, London/United Kingdom.
Eur J Cell Biol. 1996 Nov;71(3):270-6.
A reproducible technique for the ultrastructural localization of RNAs in malaria parasites has been developed which combines excellent structural preservation with high hybridization signals. Signals obtained following in situ hybridization with an antisense rRNA probe which recognizes all forms of small subunit (SSU) rRNA correlate with the density of ribosomes in the parasite cytoplasm and show that a) the male gametocyte has only 12 to 25% the ribosomes found in the female cell and asexual parasite and b) the probe did not hybridize with an electron-dense nuclear body previously called a nucleolus. We suggest this structure is either a transcription-, or a replication-factory. Using a probe for the sexual stage-specific protein Pbs21 mRNA, signal was found only in female gametocytes, zygotes and ookinetes and showed a non-random, clumped cytoplasmic distribution. It is not known at present whether the non-random distribution of the Pbs 21 mRNA is critical to the very delayed translation of the Pbs21 message into protein, which occurs only in the zygote and ookinete.
已开发出一种用于疟原虫RNA超微结构定位的可重复技术,该技术将出色的结构保存与高杂交信号相结合。用识别所有形式小亚基(SSU)rRNA的反义rRNA探针进行原位杂交后获得的信号与寄生虫细胞质中核糖体的密度相关,并表明:a)雄配子体的核糖体数量仅为雌细胞和无性寄生虫的12%至25%;b)该探针未与先前称为核仁的电子致密核体杂交。我们认为这种结构要么是转录工厂,要么是复制工厂。使用针对性别阶段特异性蛋白Pbs21 mRNA的探针,仅在雌配子体、合子和动合子中发现信号,且显示出非随机的、成簇的细胞质分布。目前尚不清楚Pbs 21 mRNA的非随机分布是否对Pbs21信息非常延迟地翻译成蛋白质至关重要,这种翻译仅发生在合子和动合子中。