Mannhaupt G, van der Linden G, Vetter I, Maurer K, Pilz U, Planta R, Feldmann H
Institut für Physiologische Chemie, Universität München, F.R.G.
Yeast. 1990 Jul-Aug;6(4):353-61. doi: 10.1002/yea.320060408.
The gene encoding threonine synthase (THR4) from the yeast Saccharomyces cerevisiae was cloned by complementation of a thr4 mutant. This gene was also found on a lambda clone (5239) consisting of a fragment of chromosome III inserted in the vector lambdaMG3. The THR4 gene encodes a protein of 514 amino acids (M.W. 58 kDa), which has extensive homologies with E. coli threonine synthase (thrC) and B subtilis threonine synthase. The 5' flanking region of the gene contains three regulatory sequences [TGACT(C)] for the general amino acid control (GCN). About 130 bp downstream of the THR4 gene another large open reading frame (563 amino acids) is found in the opposite orientation. This may imply that this open reading frame, called CTR86, shares a terminator region with THR4. The function of the protein encoded by CTR86 is not yet clear, but the fact that the upstream region contains a GCN4 responsive site suggests that the gene product may also be involved in amino acid biosynthesis.
通过互补苏氨酸营养缺陷型突变体,克隆了来自酿酒酵母的编码苏氨酸合成酶(THR4)的基因。该基因也存在于一个λ克隆(5239)上,该克隆由插入载体λMG3中的第三条染色体片段组成。THR4基因编码一个含514个氨基酸(分子量58 kDa)的蛋白质,它与大肠杆菌苏氨酸合成酶(thrC)和枯草芽孢杆菌苏氨酸合成酶有广泛的同源性。该基因的5'侧翼区域包含三个用于一般氨基酸控制(GCN)的调控序列[TGACT(C)]。在THR4基因下游约130 bp处,发现另一个大的开放阅读框(563个氨基酸),方向相反。这可能意味着这个称为CTR86的开放阅读框与THR4共享一个终止区域。CTR86编码的蛋白质的功能尚不清楚,但上游区域含有一个GCN4反应位点这一事实表明,该基因产物可能也参与氨基酸生物合成。