Gallant J A, Lindsley D
Department of Genetics, University of Washington, Seattle 98195.
J Mol Biol. 1992 Jan 5;223(1):31-40. doi: 10.1016/0022-2836(92)90713-t.
Previous experiments have shown that limitation for certain aminoacyl-tRNA species results in phenotypic suppression of a subset of frameshift mutant alleles, including members in both the (+) and (-) incorrect reading frames. Here, we demonstrate that such phenotypic suppression can occur through a ribosome reading frame shift at a hungry AAG codon calling for lysyl-tRNA in short supply. Direct amino acid sequence analysis of the product and DNA sequence manipulation of the gene demonstrate that the ribosome frameshift occurs through a movement of one base to the left, so as to decode the triplet overlapping the hungry codon from the left or 5' side, followed by continued normal translation in the new, shifted reading frame.
先前的实验表明,对某些氨酰 - tRNA种类的限制会导致一部分移码突变等位基因的表型抑制,包括(+)和( - )错误阅读框中的成员。在这里,我们证明这种表型抑制可以通过核糖体在急需赖氨酸 - tRNA的AAG密码子处发生阅读框移位来实现。对产物的直接氨基酸序列分析和基因的DNA序列操作表明,核糖体移码是通过向左移动一个碱基发生的,以便从左侧或5'端解码与急需密码子重叠的三联体,然后在新的移位阅读框中继续正常翻译。