Hou Y M, Schimmel P
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Biochemistry. 1992 Oct 27;31(42):10310-4. doi: 10.1021/bi00157a019.
A single G3:U70 base pair in the acceptor helix is the major determinant of alanine acceptance in alanine transfer RNAs. Transfer of this base pair into other transfer RNAs confers alanine acceptance. A G3:C70 substitution eliminates alanine acceptance in vivo and in vitro. In this work, a population of mutagenized G3:C70 alanine tRNA amber suppressors was subjected to a selection for mutations that compensate for the inactivating G3:C70 substitution. No compensatory mutations located in the acceptor helix were obtained. Instead, a U27:U43 substitution that replaced the wild-type C27:G43 in the anticodon stem created a U27:U43/G3:C70 mutant alanine tRNA that inserts alanine at amber codons in vivo. The U27:U43 substitution is at a location where previous footprinting work established an RNA-protein contact. Thus, this mutation may act by functionally coupling a distal part of the tRNA structure to the active site.
受体螺旋中的单个G3:U70碱基对是丙氨酸转运RNA接受丙氨酸的主要决定因素。将此碱基对转移到其他转运RNA中可赋予其接受丙氨酸的能力。G3:C70替换会在体内和体外消除丙氨酸接受能力。在这项研究中,对一群诱变的G3:C70丙氨酸tRNA琥珀抑制子进行筛选,以寻找能补偿失活的G3:C70替换的突变。未获得位于受体螺旋中的补偿性突变。相反,一个U27:U43替换(在反密码子茎中取代了野生型的C27:G43)产生了一个U27:U43/G3:C70突变丙氨酸tRNA,它能在体内的琥珀密码子处插入丙氨酸。U27:U43替换位于先前足迹分析确定有RNA-蛋白质接触的位置。因此,这种突变可能通过在功能上将tRNA结构的远端部分与活性位点偶联而起作用。