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stevor和rif是恶性疟原虫多拷贝基因家族,可能编码可变抗原。

stevor and rif are Plasmodium falciparum multicopy gene families which potentially encode variant antigens.

作者信息

Cheng Q, Cloonan N, Fischer K, Thompson J, Waine G, Lanzer M, Saul A

机构信息

The Queensland Institute of Medical Research, Royal Brisbane Hospital, Australia.

出版信息

Mol Biochem Parasitol. 1998 Nov 30;97(1-2):161-76. doi: 10.1016/s0166-6851(98)00144-3.

Abstract

Several multicopy gene families have been described in Plasmodium falciparum, including the var genes that code for the variant surface antigen PfEMP1, the stevor family of subtelomeric open reading frames and the rif interspersed repetitive elements. This report documents the chromosomal location of stevor genes, their transcription and characteristics of the deduced protein. On 14 chromosomes, 34 stevor copies were identified from the Dd2 parasite line. Most are in subtelomeric regions within 50 kb of the telomere. stevor genes are located close to var genes and rij. All stevor genes sequenced had two exons: a short exon 1 encoding a start codon and a transmembrane domain; exon 2 encoding for the remainder of the approximately 30 kDa protein and including two more transmembrane segments. A similar structure was found for copies of rif and its predicted protein. In both STEVOR and RIF proteins, a highly polymorphic region is predicted to be a loop on the outer side of the membrane. We propose that stevor and rif are members of a larger superfamily. The number of copies of stevor and rif, their location close to the var genes, their extreme polymorphism and the predicted structure of the proteins suggest that stevor and rif code for variant surface antigens.

摘要

恶性疟原虫中已发现了几个多拷贝基因家族,包括编码可变表面抗原PfEMP1的var基因、亚端粒开放阅读框的stevor家族以及rif散布重复元件。本报告记录了stevor基因的染色体定位、转录情况以及推导蛋白的特征。从Dd2寄生虫株中,在14条染色体上鉴定出了34个stevor拷贝。大多数位于端粒50 kb内的亚端粒区域。stevor基因位于var基因和rij附近。所有测序的stevor基因都有两个外显子:短的外显子1编码起始密码子和一个跨膜结构域;外显子2编码约30 kDa蛋白的其余部分,并包括另外两个跨膜片段。rif及其预测蛋白的拷贝也发现了类似结构。在STEVOR和RIF蛋白中,一个高度多态性区域预计是膜外侧的一个环。我们提出stevor和rif是一个更大超家族的成员。stevor和rif的拷贝数、它们与var基因的接近位置、它们的极端多态性以及蛋白质的预测结构表明,stevor和rif编码可变表面抗原。

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