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Transcripts of developmentally regulated Plasmodium falciparum genes quantified by real-time RT-PCR

机译:通过实时RT-PCR定量分析受发育调节的恶性疟原虫基因的转录本

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Plasmodium falciparum intraerythrocytic development is a complex process. Development proceeds rapidly from the trophozoite phase of nutrient acquisition and growth through tot he synthetic and reproductive schizont phase, which ends with production of new invasive merozoites. During this process, the malaria parasite must express a series of different gene products, depending on its metabolic and synthetic needs. We are particularly interested in the development of the merozoite's organelles in the apical complex, which form during the later schizont stages. We have used quantitative real-time RT-PCR fluorogenic 5' nuclease assays (TaqMan) for the first time on malaria parasites for analysis of erythrocytic stage-specific gene expression. We analyzed transcripts of the P.falciparum eba-175 and other erythrocyte binding-like (ebl) family genes in temperature-synchronized parasites and found ebl genes have tightly controlled, stage-specific transcription. As expected, eba-175 transcripts were abundant only at the end of schizont development in a pattern most common among ebl, including baebl, pebl and jesebl. The maebl transcript pattern was unique, peaking at mid-late trophozoite stage, but absent in late-stage schizonts. ebl-1 demonstrated another pattern of expression, which peaked during mid-schizont stage and then significantly diminished in late-stage schizonts. Our analysis demonstrates that using real-time RT-PCR fluorogenic 5' nuclease assays is a sensitive, quantitative method for analysis of Plasmodium transcripts.
机译:恶性疟原虫红细胞内发育是一个复杂的过程。从营养获取和滋养的滋养体阶段一直到合成和生殖裂殖体阶段,发展迅速,最后发展成新的侵入性裂殖子。在此过程中,疟疾寄生虫必须表达一系列不同的基因产物,这取决于其代谢和合成需求。我们对裂殖体后期形成的根尖复杂的裂殖子细胞器的发育特别感兴趣。我们首次在疟疾寄生虫上使用了定量实时RT-PCR荧光5'核酸酶测定(TaqMan),用于分析红细胞阶段特异性基因表达。我们分析了温度同步寄生虫中恶性疟原虫eba-175和其他红细胞结合样(ebl)家族基因的转录本,发现ebl基因具有严格控制的,阶段特异性的转录。如预期的那样,eba-175转录物仅在裂殖体发育结束时才丰富,并且以ebl(包括baebl,pebl和jesebl)最为常见。 maebl转录本模式是独特的,在滋养体中期晚期达到顶峰,但在后期裂殖体中则不存在。 ebl-1表现出另一种表达模式,该模式在裂殖体中期达到顶峰,而在后期裂殖体中则明显降低。我们的分析表明,使用实时RT-PCR荧光5'核酸酶测定法是分析疟原虫转录本的灵敏,定量方法。

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