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光滑念珠菌编码tRNA核苷酸转移酶的基因的鉴定

Characterization of a gene encoding tRNA nucleotidyltransferase from Candida glabrata.

作者信息

Hanic-Joyce Pamela J, Joyce Paul B M

机构信息

Department of Chemistry and Biochemistry, Concordia University, Montréal, Québec, Canada.

出版信息

Yeast. 2002 Dec;19(16):1399-411. doi: 10.1002/yea.926.

DOI:10.1002/yea.926
PMID:12478587
Abstract

A gene encoding ATP (CTP):tRNA nucleotidyltransferase (EC2.7.7.25) was isolated from Candida (Torulopsis) glabrata by complementation in Saccharomyces cerevisiae. The predicted amino acid sequence of the protein revealed a large region with high sequence similarity to members of the Class II group of the nucleotidyltransferase superfamily and an N-terminal region characteristic of a mitochondrial targeting sequence. The essential role of the carboxylates within the conserved DXD and RRD motifs was confirmed by mutagenesis. C. glabrata strains bearing truncated CCA1 genes that lacked sequences encoding the putative mitochondrial targeting peptide were unable to grow on non-fermentable carbon sources but were able to grow on a fermentable carbon source. These results suggest that, as in S. cerevisiae, the C. glabrata CCA-adding enzyme is a sorting isozyme that functions in multiple cellular compartments. Mapping of the 5'-ends of primary transcripts of CCA1 revealed multiple transcription start sites located both upstream of and between two in-frame start codons. When the cells were cultured on a non-fermentable carbon source the longer transcripts appeared more abundant, suggesting that the choice of transcription start sites was influenced by carbon source. The shorter transcripts, which lacked sequences encoding the mitochondrial targeting information, were more predominant in cells grown on glucose. These observations suggest that expression of CCA-adding isozymes in C. glabrata may be regulated. The DNA sequence has been assigned GenBank Accession No. AF098803.

摘要

通过在酿酒酵母中进行互补,从光滑念珠菌(光滑球拟酵母)中分离出了一个编码ATP(CTP):tRNA核苷酸转移酶(EC2.7.7.25)的基因。该蛋白质的预测氨基酸序列显示,有一个与核苷酸转移酶超家族II类成员具有高度序列相似性的大区域,以及一个具有线粒体靶向序列特征的N端区域。通过诱变证实了保守的DXD和RRD基序内羧酸盐的重要作用。携带截短的CCA1基因且缺乏编码假定线粒体靶向肽序列的光滑念珠菌菌株,无法在非发酵碳源上生长,但能够在发酵碳源上生长。这些结果表明,与酿酒酵母一样,光滑念珠菌的CCA添加酶是一种分选同工酶,在多个细胞区室中发挥作用。对CCA1初级转录本5'端的定位揭示了多个转录起始位点,这些位点位于两个读码框内起始密码子的上游和之间。当细胞在非发酵碳源上培养时,较长的转录本似乎更为丰富,这表明转录起始位点的选择受碳源影响。缺乏编码线粒体靶向信息序列的较短转录本,在葡萄糖培养的细胞中更为占主导。这些观察结果表明,光滑念珠菌中CCA添加同工酶的表达可能受到调控。该DNA序列已被GenBank收录,登录号为AF098803。

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引用本文的文献

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Domain movements during CCA-addition: a new function for motif C in the catalytic core of the human tRNA nucleotidyltransferases.添加CCA过程中的结构域运动:人tRNA核苷酸转移酶催化核心中基序C的新功能。
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