TY - JOUR
T1 - A regulatory gene, angR, of the iron uptake system of Vibrio anguillarum
T2 - similarity with phage P22 cro and regulation by iron
AU - Farrell, David H.
AU - Mikesell, Perry
AU - Actis, Luis A.
AU - Crosa, Jorge H.
N1 - Funding Information:
The authors wish to thank Drs. Richard Brennan and Brian Matthews for their assistance in the analysis of the helix-turn-helix domain of AngR, and Dr. Toby Bradshaw for assistance in searching the Protein Identification Resource database. This work was supported by NIH grant AIIg018 to J.H.C.
PY - 1990/1/31
Y1 - 1990/1/31
N2 - The angR locus in Vibrio anguillarum encodes a trans-acting transcriptional activator which modulates several Fe2+ -regulated loci in the anguibactin biosynthesis gene cluster. In this paper, the complete nucleotide (nt) sequence of the angR gene and deduced amino acid (aa) sequence of the AngR protein are presented. A region upstream from the angR gene is shown to have similarity with Fe2+- regulated operators in Escherichia coli which bind the Fur protein. The involvement of a Fur-like regulator is supported by transcription analysis which show that angR itself is Fe2+- regulated. The aa sequence of the AngR protein predicts a helix-turn-helix motif which shows striking homology with prokaryotic DNA-binding proteins, particularly the λ and P22 Cro proteins. In addition, there are two 18-nt regions, upstream from the angR gene, which show similarity with the oR1 and oR2 operators of P22 cro. These regions overlap with, respectively, the -35, -10 region and the putative Fur-binding region upstream from angR. These results suggest that AngR may be a DNA-binding protein which modulates Fe2+- regulated transcription and is itself Fe2+- regulated at the transcriptional level.
AB - The angR locus in Vibrio anguillarum encodes a trans-acting transcriptional activator which modulates several Fe2+ -regulated loci in the anguibactin biosynthesis gene cluster. In this paper, the complete nucleotide (nt) sequence of the angR gene and deduced amino acid (aa) sequence of the AngR protein are presented. A region upstream from the angR gene is shown to have similarity with Fe2+- regulated operators in Escherichia coli which bind the Fur protein. The involvement of a Fur-like regulator is supported by transcription analysis which show that angR itself is Fe2+- regulated. The aa sequence of the AngR protein predicts a helix-turn-helix motif which shows striking homology with prokaryotic DNA-binding proteins, particularly the λ and P22 Cro proteins. In addition, there are two 18-nt regions, upstream from the angR gene, which show similarity with the oR1 and oR2 operators of P22 cro. These regions overlap with, respectively, the -35, -10 region and the putative Fur-binding region upstream from angR. These results suggest that AngR may be a DNA-binding protein which modulates Fe2+- regulated transcription and is itself Fe2+- regulated at the transcriptional level.
KW - DNA-binding protein
KW - Sequence analysis
KW - anguibactin
KW - mRNA
KW - tranporation mutagenesis
KW - transcriptional activator
UR - http://www.scopus.com/inward/record.url?scp=0025159493&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025159493&partnerID=8YFLogxK
U2 - 10.1016/0378-1119(90)90112-5
DO - 10.1016/0378-1119(90)90112-5
M3 - Article
C2 - 2311935
AN - SCOPUS:0025159493
SN - 0378-1119
VL - 86
SP - 45
EP - 51
JO - Gene
JF - Gene
IS - 1
ER -