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利用恶性疟原虫中的稳定转染和瞬时转染对裂殖子表面蛋白-2启动子进行表征

Characterisation of the merozoite surface protein-2 promoter using stable and transient transfection in Plasmodium falciparum.

作者信息

Wickham Mark E, Thompson Jennifer K, Cowman Alan F

机构信息

The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Melbourne 3050, Australia.

出版信息

Mol Biochem Parasitol. 2003 Jul;129(2):147-56. doi: 10.1016/s0166-6851(03)00118-x.

DOI:10.1016/s0166-6851(03)00118-x
PMID:12850259
Abstract

Plasmodium falciparum merozoite surface protein (MSP)-2, is a polymorphic protein whose variable regions define two allelic families, the 3D7/IC-1 and FC27/D10 families. The gene encoding MSP-2 is located on chromosome 2 immediately 3' of the gene encoding merozoite surface protein-5 (MSP-5) with a 1096 bp intergenic region that presumably contains the MSP-2 promoter. Here we present characterization of the MSP-2 promoter using transient and stable transfection of P. falciparum. The mRNA transcription initiation site was mapped to a position 256 bp upstream of the MSP-2 translation start site. The ability of the intergenic region between MSP-5 and MSP-2 to promote the expression of chloramphenicol acetyl transferase (CAT) has been tested using a series of nested deletions in transient transfection experiments. The minimal region required for CAT expression has been defined and putative regulatory elements delineated. These nested deletions were used for heterologous expression of an FC27 family MSP-2 allele in the 3D7 allelic background in transfected 3D7 lines. In each case, the transgenic P. falciparum lines generated co-express both 3D7 and FC27 allelic forms of MSP-2 at the merozoite surface. These results have identified the functional promoter for MSP-2.

摘要

恶性疟原虫裂殖子表面蛋白(MSP)-2是一种多态性蛋白,其可变区定义了两个等位基因家族,即3D7/IC-1和FC27/D10家族。编码MSP-2的基因位于2号染色体上,紧挨着编码裂殖子表面蛋白-5(MSP-5)的基因的3'端,中间有一个1096 bp的基因间隔区,推测该区域包含MSP-2启动子。在此,我们通过恶性疟原虫的瞬时转染和稳定转染来呈现MSP-2启动子的特征。mRNA转录起始位点被定位到MSP-2翻译起始位点上游256 bp处。在瞬时转染实验中,利用一系列嵌套缺失对MSP-5和MSP-2之间的基因间隔区促进氯霉素乙酰转移酶(CAT)表达的能力进行了测试。已确定了CAT表达所需的最小区域,并划定了推定的调控元件。这些嵌套缺失用于在转染的3D7株系的3D7等位基因背景下对FC27家族MSP-2等位基因进行异源表达。在每种情况下,所产生的转基因恶性疟原虫株系在裂殖子表面共同表达MSP-2的3D7和FC27等位基因形式。这些结果确定了MSP-2的功能性启动子。

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