Certa U, Rotmann D, Matile H, Reber-Liske R
Central Research Units, F. Hoffman-La Roche and Co. Ltd., Basel, Switzerland.
EMBO J. 1987 Dec 20;6(13):4137-42. doi: 10.1002/j.1460-2075.1987.tb02759.x.
Plasmodium falciparum merozoites have variable surface proteins that are processed from a 190-kd precursor protein (p190). The gene encoding p190 exists in two allelic forms and cross-over events occurring mainly near the 5' end, combined with isolate-specific tripeptide repeats, contribute to its antigen diversity. We have sequenced a large portion of the p190 gene from the parasite isolate RO-33 (Ghana). Remarkably, the typical N-terminal tripeptide repeat structure is lacking. Apart from mutations in the variable parts, the gene appears identical to the MAD-20 allele (Papua, New Guinea). Southern blot analysis detects p190 genes similar to RO-33 in other parasite isolates independent of their geographical origin. The lack of p190 repeats in RO-33 eliminates the possibility that they are involved in host cell recognition or integration and restricts their function to immune escape.
恶性疟原虫子孢子具有可变表面蛋白,这些蛋白由一种190-kd前体蛋白(p190)加工而成。编码p190的基因存在两种等位基因形式,主要在5'端附近发生的交叉事件,与分离株特异性三肽重复序列相结合,导致其抗原多样性。我们对来自寄生虫分离株RO-33(加纳)的大部分p190基因进行了测序。值得注意的是,典型的N端三肽重复结构缺失。除了可变部分的突变外,该基因似乎与MAD-20等位基因(巴布亚新几内亚)相同。Southern印迹分析在其他寄生虫分离株中检测到与RO-33相似的p190基因,而与它们的地理来源无关。RO-33中缺乏p190重复序列,排除了它们参与宿主细胞识别或整合的可能性,并将其功能限制为免疫逃逸。