Kothe Ute, Rodnina Marina V
Institute of Physical Biochemistry, University of Witten/Herdecke, 58448 Witten, Germany.
Mol Cell. 2007 Jan 12;25(1):167-74. doi: 10.1016/j.molcel.2006.11.014.
tRNAs reading four-codon families often have a modified uridine, cmo(5)U(34), at the wobble position of the anticodon. Here, we examine the effects on the decoding mechanism of a cmo(5)U modification in tRNA(1B)(Ala), anticodon C(36)G(35)cmo(5)U(34). tRNA(1B)(Ala) reads its cognate codons in a manner that is very similar to that of tRNA(Phe). As Ala codons are GC rich and Phe codons AU rich, this similarity suggests a uniform decoding mechanism that is independent of the GC content of the codon-anticodon duplex or the identity of the tRNA. The presence of cmo(5)U at the wobble position of tRNA(1B)(Ala) permits fairly efficient reading of non-Watson-Crick and nonwobble bases in the third codon position, e.g., the GCC codon. The ribosome accepts the C-cmo(5)U pair as an almost-correct base pair, unlike third-position mismatches, which lead to the incorporation of incorrect amino acids and are efficiently rejected.
读取四密码子家族的tRNA在反密码子的摆动位置通常含有一个修饰的尿苷cmo(5)U(34)。在此,我们研究了tRNA(1B)(Ala)(反密码子为C(36)G(35)cmo(5)U(34))中cmo(5)U修饰对解码机制的影响。tRNA(1B)(Ala)读取其同源密码子的方式与tRNA(Phe)非常相似。由于丙氨酸密码子富含GC,苯丙氨酸密码子富含AU,这种相似性表明存在一种统一的解码机制,该机制独立于密码子-反密码子双链体的GC含量或tRNA的身份。tRNA(1B)(Ala)摆动位置的cmo(5)U允许在第三密码子位置相当有效地读取非沃森-克里克碱基和非摆动碱基,例如GCC密码子。核糖体将C-cmo(5)U对视为几乎正确的碱基对,这与导致错误氨基酸掺入并被有效排斥的第三位置错配不同。