Reuven N B, Zhou Z, Deutscher M P
Department of Biochemistry,University of Connecticut Health Center, Farmington, Connecticut 06030, USA.
J Biol Chem. 1997 Dec 26;272(52):33255-9. doi: 10.1074/jbc.272.52.33255.
Repair of the 3'-terminal -CCA sequence of tRNA generally requires the action of the enzyme tRNA nucleotidyltransferase. However, in Escherichia coli in the absence of this enzyme, a decreased level of tRNA end repair continues. To ascertain the enzymes responsible for this residual repair, mutant strains were constructed lacking tRNA nucleotidyltransferase and other enzymes potentially involved in the process, poly(A) polymerase I and polynucleotide phosphorylase (PNPase). Strains lacking tRNA nucleotidyltransferase and either one of the other enzymes displayed decreased growth rates and increased levels of defective tRNA compared with the single cca mutant. Triple mutants lacking all three enzymes grew very slowly, had even more defective tRNA, and were devoid of activity incorporating AMP into tRNA-C-C. Overexpression of poly(A) polymerase I, but not PNPase, partially compensated for the absence of tRNA nucleotidyltransferase. These data show that poly(A) polymerase I and PNPase participate in the end repair process and are required to maintain functional tRNA levels when tRNA nucleotidyltransferase is absent.
tRNA 3'-末端-CCA序列的修复通常需要tRNA核苷酸转移酶的作用。然而,在缺乏这种酶的大肠杆菌中,tRNA末端修复水平仍会降低。为了确定负责这种残余修复的酶,构建了缺乏tRNA核苷酸转移酶以及其他可能参与该过程的酶(聚腺苷酸聚合酶I和多核苷酸磷酸化酶(PNPase))的突变菌株。与单个cca突变体相比,缺乏tRNA核苷酸转移酶和其他一种酶的菌株生长速率降低,有缺陷的tRNA水平增加。缺乏所有三种酶的三重突变体生长非常缓慢,有更多有缺陷的tRNA,并且没有将AMP掺入tRNA-C-C的活性。聚腺苷酸聚合酶I(而非PNPase)的过表达部分补偿了tRNA核苷酸转移酶的缺失。这些数据表明,聚腺苷酸聚合酶I和PNPase参与末端修复过程,并且在缺乏tRNA核苷酸转移酶时是维持功能性tRNA水平所必需的。