Vernick K D, Walliker D, McCutchan T F
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892.
Nucleic Acids Res. 1988 Jul 25;16(14B):6973-85. doi: 10.1093/nar/16.14.6973.
Sequences related to those near chromosome telomeres in the human malaria parasite, Plasmodium falciparum, were extremely unstable during a genetic cross between two different clonal genotypes. Many progeny of the heterologous cross displayed telomere-homologous restriction fragments found in neither parent. A significant number of the new fragments resulted from rearrangements at chromosome-internal locations which were bounded by more complex tracts of DNA sequence. The same instability was not seen to arise during an inbreeding cross, nor during mitotic replication of parasites. Thus, a form of genetic hypervariability results from molecular events which occur during meiotic reduction and is apparent only in a cross between heterologous strains of parasite. Since other sequences were entirely stable under the same conditions, it appears that chromosome-internal blocks of telomeric sequences in the P. falciparum genome may designate conditionally unstable chromosomal domains. We discuss some potential implications of these findings for the population biology of P. falciparum.
在人类疟原虫恶性疟原虫中,与染色体端粒附近序列相关的序列在两种不同克隆基因型之间的遗传杂交过程中极其不稳定。异源杂交的许多后代显示出在双亲中均未发现的端粒同源限制性片段。相当数量的新片段源于染色体内部位置的重排,这些位置由更复杂的DNA序列片段界定。在近亲杂交过程中以及寄生虫的有丝分裂复制过程中均未观察到同样的不稳定性。因此,一种遗传高变异性源于减数分裂减数过程中发生的分子事件,并且仅在寄生虫异源菌株之间的杂交中明显。由于其他序列在相同条件下完全稳定,因此恶性疟原虫基因组中的染色体内部端粒序列块似乎可能指定有条件不稳定的染色体结构域。我们讨论了这些发现对恶性疟原虫种群生物学的一些潜在影响。