Langford C K, Ewbank S A, Hanson S S, Ullman B, Landfear S M
Department of Microbiology and Immunology, Oregon Health Sciences University, Portland 97201.
Mol Biochem Parasitol. 1992 Oct;55(1-2):51-64. doi: 10.1016/0166-6851(92)90126-5.
The polymerase chain reaction was used to clone two genes from Leishmania donovani, each of which encodes a member of a superfamily of membrane transporters which include the mammalian facilitative glucose transporters. One of these transporters, designated D2, is similar in sequence and overall structural features to a previously cloned Leishmania transporter Pro-1. Both D2 and Pro-1 are developmentally regulated genes which are expressed primarily in the insect stage of the parasite life cycle. In contrast, the second novel transporter, D1, is structurally quite different from either D2 or Pro-1, and its expression is not regulated during the parasite life cycle. All three genes are located on different chromosomes in L. donovani.
聚合酶链反应被用于从杜氏利什曼原虫中克隆两个基因,每个基因编码一个膜转运蛋白超家族的成员,该超家族包括哺乳动物易化葡萄糖转运蛋白。其中一种转运蛋白命名为D2,其序列和整体结构特征与先前克隆的利什曼原虫转运蛋白Pro-1相似。D2和Pro-1都是发育调控基因,主要在寄生虫生命周期的昆虫阶段表达。相比之下,第二个新的转运蛋白D1在结构上与D2或Pro-1有很大不同,并且其表达在寄生虫生命周期中不受调控。这三个基因都位于杜氏利什曼原虫的不同染色体上。