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发根诱导质粒pRiA4的调控蛋白VirG的推定起始密码子TTG。

Putative start codon TTG for the regulatory protein VirG of the hairy-root-inducing plasmid pRiA4.

作者信息

Aoyama T, Hirayama T, Tamamoto S, Oka A

机构信息

Laboratory of Molecular Biology, Institute for Chemical Research, Kyoto University, Japan.

出版信息

Gene. 1989 May 15;78(1):173-8. doi: 10.1016/0378-1119(89)90325-9.

Abstract

The nucleotide sequence of the virG gene for a transcriptional activator on the agropine-type hairy-root-inducing plasmid pRiA4 was determined. The sequence contained one possible open reading frame. The gene product with a molecular size of 26.5 kDa was identified by an Escherichia coli coupled-transcription-translation system using cloned virG plasmids as templates. However, neither an ATG nor a GTG start codon which could give rise to such a protein was identified in the nucleotide sequence. Instead, TTG was found as a candidate for the start codon. This TTG was preceded, like most other TTG start codons, by both a Shine-Dalgarno (SD) sequence and a T signal which are respectively complementary to the 3'-end region of 16S rRNA and the T psi loop of initiator tRNA. Further evidence for the start at TTG was obtained by gene fusion experiments. When the E. coli lacZ gene, whose expression entirely depends on the transcription and translation from upstream regions, was connected in-phase with virG either directly upstream or downstream of the TTG sequence, only the latter fused gene expressed the beta-galactosidase activity in Agrobacterium cells in response to a plant phenolic compound, acetosyringone. The TTG codon preceded by an SD sequence and a T signal is also conserved in the virG sequences from other three tumor-inducing plasmids previously reported.

摘要

测定了农杆碱型发根诱导质粒pRiA4上转录激活因子virG基因的核苷酸序列。该序列包含一个可能的开放阅读框。使用克隆的virG质粒作为模板,通过大肠杆菌偶联转录-翻译系统鉴定出分子大小为26.5 kDa的基因产物。然而,在核苷酸序列中未鉴定到可产生这种蛋白质的ATG或GTG起始密码子。相反,发现TTG是起始密码子的候选者。与大多数其他TTG起始密码子一样,该TTG之前有一个与16S rRNA的3'端区域互补的Shine-Dalgarno(SD)序列和一个与起始tRNA的T ψ环互补的T信号。通过基因融合实验获得了更多关于从TTG起始的证据。当完全依赖上游区域转录和翻译的大肠杆菌lacZ基因与virG在TTG序列的直接上游或下游同相位连接时,只有后者的融合基因在农杆菌细胞中响应植物酚类化合物乙酰丁香酮时表达β-半乳糖苷酶活性。在先前报道的其他三种致瘤质粒的virG序列中,由SD序列和T信号之前的TTG密码子也保守存在。

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