Murgola E J, Pagel F T, Hijazi K A
J Mol Biol. 1984 May 5;175(1):19-27. doi: 10.1016/0022-2836(84)90442-x.
After our first observation of codon context effects in missense suppression ( Murgola & Pagel , 1983), we measured the suppression of missense mutations at two positions in trpA in Escherichia coli. The suppressible codons in the trpA messenger RNA were the lysine codons, AAA and AAG, and the glutamic acid codons, GAA and GAG. The mRNA sites of the codons correspond to amino acids 211 and 234 of the trpA polypeptide, positions at which glycine is the wild-type amino acid. Our data demonstrated codon context effects with both pairs of codons. The results indicate that suppression of AAA and AAG by mutant lysine transfer RNAs was more efficient at 211 than at 234, whereas suppression of GAA and GAG by two different mutant glycine tRNAs was more efficient at 234 than at 211. In general, the context effects were more pronounced with GAG and AAG than with GAA and AAA. (In some instances it appeared that suppression of GAA or AAA at a given position was more effective than suppression of GAG or AAG.) By contrast, no context effects were observed with a glyT suppressor of AAA and AAG, a glyT GAA/G-suppressor, and a glyU suppressor of GAG. Our observation of this phenomenon in missense suppression demonstrates that codon context can affect polypeptide elongation and that the effects can be different depending on the codons and tRNAs examined. It is suggested that tRNA-tRNA interaction on the ribosome is involved in the observed context effects.
在我们首次观察到错义抑制中的密码子上下文效应(Murgola & Pagel,1983)之后,我们测量了大肠杆菌中trpA基因两个位置上错义突变的抑制情况。trpA信使RNA中的可抑制密码子是赖氨酸密码子AAA和AAG,以及谷氨酸密码子GAA和GAG。这些密码子在mRNA上的位点对应于trpA多肽的第211和234位氨基酸,野生型氨基酸在此位置为甘氨酸。我们的数据表明这两对密码子都存在密码子上下文效应。结果表明,突变的赖氨酸转运RNA对AAA和AAG的抑制在211位比在234位更有效,而两种不同的突变甘氨酸tRNA对GAA和GAG的抑制在234位比在211位更有效。一般来说,GAG和AAG的上下文效应比GAA和AAA更明显。(在某些情况下,给定位置上GAA或AAA的抑制似乎比GAG或AAG的抑制更有效。)相比之下,对于AAA和AAG的glyT抑制子、glyT GAA/G抑制子以及GAG的glyU抑制子,未观察到上下文效应。我们在错义抑制中对这一现象的观察表明,密码子上下文可以影响多肽延伸,并且根据所检测的密码子和tRNA不同,这种影响也会不同。有人提出,核糖体上的tRNA - tRNA相互作用与所观察到的上下文效应有关。