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GCV3的分子特征,即编码甘氨酸裂解系统氢载体蛋白的酿酒酵母基因。

Molecular characterization of GCV3, the Saccharomyces cerevisiae gene coding for the glycine cleavage system hydrogen carrier protein.

作者信息

Nagarajan L, Storms R K

机构信息

Department of Chemistry and Biochemistry and the Department of Biology, Concordia University, Montreal, Quebec H3G 1M8, Canada.

出版信息

J Biol Chem. 1997 Feb 14;272(7):4444-50. doi: 10.1074/jbc.272.7.4444.

Abstract

YAL044, a gene on the left arm of Saccharomyces cerevisiae chromosome one, is shown to code for the H-protein subunit of the multienzyme glycine cleavage system. The gene designation has therefore been changed to GCV3, reflecting its role in the glycine cleavage system. GCV3 encodes a 177-residue protein with a putative mitochondrial targeting signal at its amino terminus. Targeted gene replacement shows that GCV3 is not required for growth on minimal medium; however, it is essential when glycine serves as the sole nitrogen source. Studies of GCV3 expression revealed that it is highly regulated. Supplementation of minimal medium with glycine, the glycine cleavage system's substrate, induced expression at least 30-fold. In contrast, and consistent with the cleavage of glycine providing activated single-carbon units, the addition of the metabolic end products that require activated single-carbon units repressed expression about 10-fold. Finally, like many amino acid biosynthetic genes, GCV3 is subject to regulation by the general amino acid control system.

摘要

YAL044是酿酒酵母一号染色体左臂上的一个基因,已证明它编码多酶甘氨酸裂解系统的H蛋白亚基。因此,该基因命名已改为GCV3,以反映其在甘氨酸裂解系统中的作用。GCV3编码一个177个残基的蛋白质,在其氨基末端有一个假定的线粒体靶向信号。靶向基因置换表明,在基本培养基上生长不需要GCV3;然而,当甘氨酸作为唯一氮源时,它是必不可少的。对GCV3表达的研究表明,它受到高度调控。用甘氨酸(甘氨酸裂解系统的底物)补充基本培养基可诱导其表达至少30倍。相反,与甘氨酸裂解产生活化的单碳单位一致,添加需要活化单碳单位的代谢终产物可使表达抑制约10倍。最后,与许多氨基酸生物合成基因一样,GCV3受一般氨基酸控制系统的调控。

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