Gallant J, Erlich H, Weiss R, Palmer L, Nyari L
Mol Gen Genet. 1982;186(2):221-7. doi: 10.1007/BF00331853.
A number of nonsense alleles of lacZ exhibit phenotypic suppression (as much as a sixteen-fold increase in leakiness) during partial limitation for certain aminoacyl-tRNA species in relA mutant cells. Each responsive allele has its individual pattern of response to limitation for one or more amino acids or aminoacyl-tRNA's. The phenotypic suppression occurs only during limitation, and ceases once limitation is reversed. Suppression is much reduced by the presence of the relA+ allele or an allele of rpsL which restricts ribosomal ambiguity. In one case, the suppressed product has been identified by radioimmune assay and gel electrophoresis, and is a full-length lacZ protomer. Mechanisms are discussed whereby aberrations of translation at codons calling for an aminoacyl-tRNA species in short supply might lead to readthrough of a nearby nonsense codon.
在relA突变细胞中,当某些氨酰-tRNA种类部分受限期间,许多lacZ的无义等位基因表现出表型抑制(渗漏增加多达16倍)。每个响应等位基因对一种或多种氨基酸或氨酰-tRNA受限都有其独特的响应模式。表型抑制仅在受限期间发生,一旦受限情况逆转就会停止。relA+等位基因或限制核糖体模糊性的rpsL等位基因的存在会大大降低抑制作用。在一个案例中,通过放射免疫测定和凝胶电泳鉴定出了被抑制的产物,它是一个全长的lacZ原体。文中讨论了一些机制,即对供应不足的氨酰-tRNA种类的密码子处翻译异常可能导致附近无义密码子的通读。