Lanzer M, de Bruin D, Ravetch J V
DeWitt Wallace Research Laboratory, Sloan-Kettering Institute, Division of Molecular Biology, New York, New York 10021.
Nature. 1993 Feb 18;361(6413):654-7. doi: 10.1038/361654a0.
Classical genetic studies on the human malaria parasite Plasmodium falciparum have been hampered by a complex life cycle which alternates between vertebrate and invertebrate hosts. Consequently, only a few genetic crosses have been performed so far. In addition, molecular genetics has provided only limited access to the genes of this pathogen, a consequence of an unusually high A + T content. To overcome these limitations we have constructed an ordered telomere-to-telomere contig map of P. falciparum chromosome 2 by isolating overlapping yeast artificial chromosome clones. This approach was used to examine the strain-dependent polymorphisms commonly observed for P. falciparum chromosomes. Our analysis reveals that polymorphisms of chromosome 2 are restricted to regions at either end, representing 20% of the chromosome. Transcription mapping of the entire chromosome suggests a compartmentalization of chromosome 2 into a transcribed central domain and silent polymorphic ends.
对人类疟原虫恶性疟原虫的经典遗传学研究一直受到其复杂生命周期的阻碍,该生命周期在脊椎动物和无脊椎动物宿主之间交替。因此,到目前为止只进行了少数遗传杂交实验。此外,由于异常高的A + T含量,分子遗传学对该病原体基因的研究也非常有限。为了克服这些限制,我们通过分离重叠的酵母人工染色体克隆构建了恶性疟原虫2号染色体的端粒到端粒的有序重叠群图谱。该方法用于研究恶性疟原虫染色体常见的菌株依赖性多态性。我们的分析表明,2号染色体的多态性仅限于两端区域,占染色体的20%。对整个染色体的转录图谱分析表明,2号染色体可分为一个转录的中央结构域和沉默的多态性末端。