Scherf A, Carter R, Petersen C, Alano P, Nelson R, Aikawa M, Mattei D, Pereira da Silva L, Leech J
Unité de Parasitologie Expérimentale, CNRS URA 361, Institut Pasteur, Paris, France.
EMBO J. 1992 Jun;11(6):2293-301. doi: 10.1002/j.1460-2075.1992.tb05288.x.
We report the identification of the product of the Plasmodium falciparum Pf11-1 gene and demonstrate that it is a gametocyte-specific protein that has a potential role in the rupture of the host erythrocyte and emergence of the gametes (gametogenesis). The Pf11-1 gene is a large locus (30 kb) whose sequence predicts a glutamic acid-rich polypeptide. Our identification of the Pf11-1 gene product as gametocyte specific was greatly facilitated by the isolation of a mutant parasite clone in which greater than 90% of the Pf11-1 gene was deleted. Molecular analysis of the mutant locus suggests that the underlying genetic mechanism is chromosome breakage and subsequent healing by the addition of telomere repeats. PCR-based analysis showed that similar DNA rearrangements occur commonly in small subpopulations of most laboratory strains, suggesting that the Pf11-1 locus represents a fragile chromosome region. Northern blot analysis demonstrates that a large Pf11-1 gene-specific transcript (much greater than 10 kb) is present in gametocytes but not in asexual blood stage parasites. The Pf11-1 protein was localized by electron microscopy to granules in the cytoplasm of gametocytes adjacent to the membrane of the parasitophorous vacuole. Following in vitro stimulation of gametogenesis, the Pf11-1 protein was found in the membrane of lysed erythrocytes, suggesting a role for Pf11-1 in erythrocyte rupture within the mosquito gut.
我们报告了恶性疟原虫Pf11-1基因产物的鉴定,并证明它是一种配子体特异性蛋白,在宿主红细胞破裂和配子出现(配子发生)过程中具有潜在作用。Pf11-1基因是一个大的基因座(30 kb),其序列预测有一个富含谷氨酸的多肽。通过分离一个突变寄生虫克隆,其中超过90%的Pf11-1基因被删除,极大地促进了我们对Pf11-1基因产物作为配子体特异性的鉴定。对突变基因座的分子分析表明,潜在的遗传机制是染色体断裂以及随后通过添加端粒重复序列进行修复。基于PCR的分析表明,类似的DNA重排在大多数实验室菌株的小亚群中普遍存在,这表明Pf11-1基因座代表一个脆弱的染色体区域。Northern印迹分析表明,一个大的Pf11-1基因特异性转录本(远大于10 kb)存在于配子体中,但不存在于无性血液阶段的寄生虫中。通过电子显微镜将Pf11-1蛋白定位到配子体细胞质中与寄生泡膜相邻的颗粒中。在体外刺激配子发生后,在裂解红细胞的膜中发现了Pf11-1蛋白,这表明Pf11-1在蚊子肠道内的红细胞破裂中起作用。