An early step in wobble uridine tRNA modification requires the Elongator complex

被引:360
作者
Huang, B [1 ]
Johansson, MJO [1 ]
Byström, AS [1 ]
机构
[1] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
关键词
5-methoxycarbonylmethyl-2-thiouridine; 5-methoxycarbonylmethyluridine; 5-carbamoylmethyluridine; Elongator complex; KTI genes;
D O I
10.1261/rna.7247705
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Elongator has been reported to be a histone acetyltransferase complex involved in elongation of RNA polymerase 11 transcription. In Saccharomyces cerevisiae, mutations in any of the six Elongator protein subunit (ELP1-ELP6) genes or the three killer toxin insensitivity (KTI11-KTI13) genes cause similar pleiotropic phenotypes. By analyzing modified nucleosides in individual tRNA species, we show that the ELP1-ELP6 and KTI11-KTI13 genes are all required for an early step in synthesis of 5-methoxycarbonylmethyl (mcm(5)) and 5-carbamoylmethyl (ncm(5)) groups present on uridines at the wobble position in tRNA. Transfer RNA immunoprecipitation experiments showed that the Elp1 and Elp3 proteins specifically coprecipitate a tRNA susceptible to formation of an mcm(5) side chain, indicating a direct role of Elongator in tRNA modification. The presence of mcm(5)U, ncm(5)U, or derivatives thereof at the wobble position is required for accurate and efficient translation, suggesting that the phenotypes of elp1-elp6 and kti11-kti13 mutants could be caused by a translational defect. Accordingly, a deletion of any ELP1-ELP6 or. KTI11-KTI13 gene prevents an ochre suppressor tRNA that normally contains mcm(5)U from reading ochre stop codons.
引用
收藏
页码:424 / 436
页数:13
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