IDENTIFICATION OF AMINO-ACIDS INSERTED DURING SUPPRESSION OF UAA AND UGA TERMINATION CODONS AT THE GAG-POL JUNCTION OF MOLONEY MURINE LEUKEMIA-VIRUS

被引:81
作者
FENG, YX
COPELAND, TD
OROSZLAN, S
REIN, A
LEVIN, JG
机构
[1] NICHHD, MOLEC GENET LAB, BETHESDA, MD 20892 USA
[2] NCI, FREDERICK CANC RES & DEV CTR, BASIC RES PROGRAM, ADV BIOSCI LABS, FREDERICK, MD 21701 USA
关键词
codon context; genetic code; retroviruses; translational readthrough; tRNA;
D O I
10.1073/pnas.87.22.8860
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Expression of the murine leukemia virus pol gene occurs by translational readthrough of an in-frame UAG codon between the gag and pol coding regions. In a previous study, we mutated the UAG codon to UAA or UGA and demonstrated that both of these termination codons could be suppressed in reticulocyte lysates and in infected cells with the same efficiency as UAG. We now report the identity of the amino acids inserted in vitro in response to UAA and UGA in fusion products containing the gag-pol junction region. The results show that UAA, like UAG, directs the incorporation of glutamine, whereas UGA directs the incorporation of three amino acids, arginine, cysteine, and tryptophan. To our knowledge, this is the first report indicating misreading of UAA as glutamine and UGA as arginine and cysteine in higher eukaryotes. Interestingly, although our protein synthesis system presumably contains other known UAG and UGA suppressors, these tRNAs did not suppress the termination codons in our experiments. Thus, it seems possible that the sequence surrounding the gag-pol junction not only promotes suppression but also helps determine which tRNAs function in suppression.
引用
收藏
页码:8860 / 8863
页数:4
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