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微小隐孢子虫基因组中编码ABC系统的序列的比较分析。

Comparative analysis of sequences encoding ABC systems in the genome of the microsporidian Encephalitozoon cuniculi.

作者信息

Cornillot Emmanuel, Metenier Guy, Vivares Christian P, Dassa Elie

机构信息

Parasitologie moléculaire et cellulaire, LBP, UMR CNRS 6023, Université Blaise Pascal, 63177 Aubière Cedex, France.

出版信息

FEMS Microbiol Lett. 2002 Apr 23;210(1):39-47. doi: 10.1111/j.1574-6968.2002.tb11157.x.

Abstract

Microsporidia are amitochondriate eukaryotic microbes with fungal affinities and a common status of obligate intracellular parasites. A set of 13 potential genes encoding ATP-binding cassette (ABC) systems was identified in the fully sequenced genome of Encephalitozoon cuniculi. Our analyses of multiple alignments, phylogenetic trees and conserved motifs support a distribution of E. cuniculi ABC systems within only four subfamilies. Six half transporters are homologous to the yeast ATM1 mitochondrial protein, a finding which is in agreement with the hypothesis of a cryptic mitochondrion-derived compartment playing a role in the synthesis and transport of Fe-S clusters. Five half transporters are similar to the human ABCG1 and ABCG2 proteins, involved in regulation of lipid trafficking and anthracyclin resistance respectively. Two proteins with duplicated ABC domains are clearly candidate to non-transport ABC systems: the first is homologous to mammalian RNase L inhibitor and the second to the yeast translation initiation regulator GCN20. An unusual feature of ABC systems in E. cuniculi is the lack of homologs of P-glycoprotein and other ABC transporters which are involved in multiple drug resistance in a large number of eukaryotic microorganisms.

摘要

微孢子虫是一类与真菌有亲缘关系的无线粒体真核微生物,属于专性细胞内寄生虫。在已完成全基因组测序的兔脑炎微孢子虫中,鉴定出一组13个潜在的编码ATP结合盒(ABC)系统的基因。我们对多序列比对、系统发育树和保守基序的分析支持兔脑炎微孢子虫ABC系统仅分布在四个亚科中。六个半转运蛋白与酵母ATM1线粒体蛋白同源,这一发现与一种隐秘的线粒体衍生区室在铁硫簇的合成和转运中起作用的假说一致。五个半转运蛋白与人类ABCG1和ABCG2蛋白相似,分别参与脂质转运调节和蒽环类抗生素抗性。两个具有重复ABC结构域的蛋白显然是非转运ABC系统的候选蛋白:第一个与哺乳动物RNase L抑制剂同源,第二个与酵母翻译起始调节因子GCN20同源。兔脑炎微孢子虫ABC系统的一个不寻常特征是缺乏P-糖蛋白和其他ABC转运蛋白的同源物,而这些蛋白在大量真核微生物中参与多重耐药性。

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