TY - JOUR
T1 - Putative start codon TTG for the regulatory protein VirG of the hairy-root-inducing plasmid pRiA4
AU - Takashi, Aoyama
AU - Takashi, Hirayama
AU - Satoshi, Tamamoto
AU - Atsuhiro, Oka
N1 - Funding Information:
We thank Dr. T. Itoh for a gift of pMY 12-6A. This work was supported in part by Grants-in-Aid for Scientific Research from the Ministry of Education, Science and Culture of Japan (62480463)a nd from Yamada Science Foundation.
PY - 1989/5/15
Y1 - 1989/5/15
N2 - The nucleotide sequence of the virG gene for a transcriptional activator on the agropine-type hairy-rootinducing 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 Tψ/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 β-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.
AB - The nucleotide sequence of the virG gene for a transcriptional activator on the agropine-type hairy-rootinducing 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 Tψ/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 β-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.
KW - Recombinant DNA
KW - Ri and Ti plasmids
KW - acetosyringone
KW - agropine-type
KW - plant phenolic compounds
KW - plasmid evolution
KW - positive regulator
KW - transcriptional activator
KW - transformation
KW - virulence gene
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U2 - 10.1016/0378-1119(89)90325-9
DO - 10.1016/0378-1119(89)90325-9
M3 - Article
C2 - 2670679
AN - SCOPUS:0024970322
SN - 0378-1119
VL - 78
SP - 173
EP - 178
JO - Gene
JF - Gene
IS - 1
ER -