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恶性疟原虫血液期表达的大核糖体亚基rRNA的结构

The structure of the large subunit rRNA expressed in blood stages of Plasmodium falciparum.

作者信息

Waters A P, White W, McCutchan T F

机构信息

Growth and Development Section, National Institutes of Health, Bethesda, MD 20892-0425, USA.

出版信息

Mol Biochem Parasitol. 1995 Jun;72(1-2):227-37. doi: 10.1016/0166-6851(94)00077-z.

Abstract

Here we present the sequence of the large subunit (LSU) rRNA expressed in blood-stage forms (and therefore A-type) of the malaria parasite, Plasmodium falciparum, from two different isolates. We determined the genomic sequence of a rRNA unit of the CAMP parasite strain from within the internal transcribed spacer 1 (ITS1) through the 5.8S rRNA gene, the ITS2 and the entire large subunit rRNA gene. We have also determined the corresponding sequence of the gene of the FVO strain by sequencing cDNA clones derived from blood-stage asexual parasites. Differences between the two were due to scattered point mutations in expansion segments of the mature rRNA regions. In addition to the point mutations, the rRNA genes from the two strains could be distinguished by the presence of a more complex polymorphism near the 3' end of the molecule. The most complex polymorphic form was localized on a single chromosome and found in only a subset of geographically distinct isolates. The sequences of the 5.8S rRNA unit and the LSU rRNA unit reported here can be logically assembled into a complete secondary structure which conforms to the standard structure conserved in all eukaryotic ribosomes. The construction of a model of secondary structure for the LSU rRNA has allowed the identification of phylogenetically conserved sequences involved in drug interaction with the ribosome, as well as those sequences involved in tertiary interactions within the rRNA itself.

摘要

在此,我们展示了来自两种不同分离株的恶性疟原虫血液阶段形式(因此为A型)中表达的大核糖体亚基(LSU)rRNA的序列。我们确定了CAMP寄生虫株rRNA单位从内部转录间隔区1(ITS1)到5.8S rRNA基因、ITS2以及整个大核糖体亚基rRNA基因的基因组序列。我们还通过对来自血液阶段无性寄生虫的cDNA克隆进行测序,确定了FVO株基因的相应序列。两者之间的差异是由于成熟rRNA区域扩展段中的散在点突变。除了点突变外,两种菌株的rRNA基因还可通过分子3'端附近存在更复杂的多态性来区分。最复杂的多态形式位于一条染色体上,且仅在地理上不同的分离株的一个子集中发现。本文报道的5.8S rRNA单位和LSU rRNA单位的序列可以合理地组装成一个完整的二级结构,该结构符合所有真核核糖体中保守的标准结构。LSU rRNA二级结构模型的构建使得能够识别与核糖体药物相互作用相关的系统发育保守序列,以及rRNA自身内三级相互作用相关的序列。

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