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乳酸克鲁维酵母中编码18S rRNA的m2(6)A二甲基化酶的KlDIM1基因的克隆与特性分析

Cloning and characterization of the KlDIM1 gene from Kluyveromyces lactis encoding the m2(6)A dimethylase of the 18S rRNA.

作者信息

Housen I, Demonté D, Lafontaine D, Vandenhaute J

机构信息

Unité de Recherches en Biologie Moléculaire, Facultés Notre-Dame de la Paix, Namur, Belgium.

出版信息

Yeast. 1997 Jun 30;13(8):777-81. doi: 10.1002/(SICI)1097-0061(19970630)13:8<777::AID-YEA140>3.0.CO;2-1.

Abstract

The KlDIM1 gene encoding the m2(6)A rRNA dimethylase was cloned from a Kluyveromyces lactis genomic library using a PCR amplicon from the Saccharomyces cerevisiae ScDIM1 gene as probe. The KlDIM1 gene encodes a 320-amino acid protein which shows 81% identity to ScDim1p from S. cerevisiae and 25% identity to ksgAp from Escherichia coli. Complementation of the kasugamycin-resistant ksgA-mutant of E. coli lacking dimethylase activity demonstrates that KlDim1p is the functional homologue of the bacterial enzyme. Multiple alignment of dimethylases from prokaryotes and yeasts shows that the two yeast enzymes display distinctive structural motives including a putative nuclear localization signal.

摘要

使用来自酿酒酵母ScDIM1基因的PCR扩增子作为探针,从乳酸克鲁维酵母基因组文库中克隆了编码m2(6)A rRNA二甲基化酶的KlDIM1基因。KlDIM1基因编码一种320个氨基酸的蛋白质,与酿酒酵母的ScDim1p有81%的同一性,与大肠杆菌的ksgAp有25%的同一性。对缺乏二甲基化酶活性的大肠杆菌卡那霉素抗性ksgA突变体的互补实验表明,KlDim1p是该细菌酶的功能同源物。原核生物和酵母中二甲基化酶的多序列比对表明,这两种酵母酶表现出独特的结构基序,包括一个假定的核定位信号。

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