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粟酒裂殖酵母10kb DNA片段上arg3和arg11基因的克隆与测序。其翻译产物的异源表达及线粒体靶向定位。

Cloning and sequencing of arg3 and arg11 genes of Schizosaccharomyces pombe on a 10-kb DNA fragment. Heterologous expression and mitochondrial targeting of their translation products.

作者信息

Van Huffel C, Dubois E, Messenguy F

机构信息

Laboratoire de Microbiologie, Universite Libre de Bruxelles, Belgium.

出版信息

Eur J Biochem. 1992 Apr 1;205(1):33-43. doi: 10.1111/j.1432-1033.1992.tb16749.x.

Abstract

The Schizosaccharomyces pombe arginine anabolic genes encoding ornithine carbamoyltransferase (arg3) and acetylglutamate kinase/acetylglutamyl-phosphate reductase (arg11) were cloned by functional complementation of S. pombe arg3 and arg11 mutant strains from S. pombe DNA genomic libraries. Restriction analysis and sequencing of the two clones showed that both genes are located on a common DNA fragment. The arg3 gene encodes a 327-amino-acid polypeptide presenting a strong identity to Saccharomyces cerevisiae and human ornithine carbamoyltransferases. The arg11 gene encodes a 884-amino-acid polypeptide. The acetylglutamate kinase and acetylglutamate-phosphate reductase domains have been defined by their identity with the S. cerevisiae ARG5,6 protein. The cloned arg11 gene from S. pombe does not complement an arg5,6 mutation in S. cerevisiae, nor does the ARG5,6 gene complement the S. pombe arg11- mutation. In contrast, both ornithine-carbamoyltransferase-encoding genes function in S. pombe. However, the S. pombe arg3 gene complements only weakly an arg3 S. cerevisiae strain, which is in agreement with the low level of expression of the S. pombe gene in S. cerevisiae. The subcellular localization of both ornithine carbamoyltransferases in the two yeasts indicates that, in contrast to the S. pombe enzyme, more than 95% of the S. cerevisiae enzyme remains in the S. pombe cytoplasm. The low expression of S. pombe ornithine carbamoyltransferases in S. cerevisiae did not allow its localization. The promoters of S. pombe arg3 and arg11 genes do not present striking similarities among themselves nor with the promoters of the equivalent genes of S. cerevisiae.

摘要

通过来自粟酒裂殖酵母DNA基因组文库对粟酒裂殖酵母arg3和arg11突变株进行功能互补,克隆了编码鸟氨酸氨甲酰基转移酶(arg3)和乙酰谷氨酸激酶/乙酰谷氨酰磷酸还原酶(arg11)的粟酒裂殖酵母精氨酸合成基因。对这两个克隆进行的限制性分析和测序表明,这两个基因位于一个共同的DNA片段上。arg3基因编码一个327个氨基酸的多肽,与酿酒酵母和人类鸟氨酸氨甲酰基转移酶具有高度同源性。arg11基因编码一个884个氨基酸的多肽。乙酰谷氨酸激酶和乙酰谷氨酸磷酸还原酶结构域已通过与酿酒酵母ARG5,6蛋白的同源性得以确定。从粟酒裂殖酵母中克隆的arg11基因不能互补酿酒酵母中的arg5,6突变,同样,ARG5,6基因也不能互补粟酒裂殖酵母的arg11突变。相反,两个编码鸟氨酸氨甲酰基转移酶的基因在粟酒裂殖酵母中都能发挥作用。然而,粟酒裂殖酵母arg3基因对酿酒酵母arg3菌株的互补作用较弱,这与粟酒裂殖酵母基因在酿酒酵母中的低表达水平相一致。两种酵母中鸟氨酸氨甲酰基转移酶的亚细胞定位表明,与粟酒裂殖酵母的酶不同,超过95%的酿酒酵母酶保留在粟酒裂殖酵母的细胞质中。粟酒裂殖酵母鸟氨酸氨甲酰基转移酶在酿酒酵母中的低表达使其无法定位。粟酒裂殖酵母arg3和arg11基因的启动子彼此之间以及与酿酒酵母等效基因的启动子之间没有显著的相似性。

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