TY - JOUR
T1 - Overlapping divergent promoters control expression of Tn10 tetracycline resistance
AU - Bertrand, Kevin P.
AU - Postle, Kathleen
AU - Wray, Lewis V.
AU - Reznikoff, William S.
N1 - Funding Information:
We thank Mrs. Rhonda Good for excellent technical assistance, Drs. Craig Adams, Kenneth Draper, and Edward Wagner for helpful discussions and Dr. Wolfgang Hillen for ~mmunicating results prior to publication. This work was supported by grants from the National Institutes of Health. Work conducted at the University of California was supported by Research Grant AI 16735 (K.P.B.), Research Fellowship F32 GM06702 (K.P.), and Research Career Development Award AI00470 (K.P.B.). Work conducted at the University of Wisconsin was supported by Oncogenic Virus Training Grant CA09075 (K.P.B.), Predoctoral Training Grant GM072 15 (L.V.W.), and Research Grant GM19670 (W.S.R.).
PY - 1983/8
Y1 - 1983/8
N2 - We have previously examined the genetic organization and regulation of the Tn10 tetracycline-resistance determinant in Escherichia coli K-12. The structural genes for tetA, the Tn10 tetracycline-resistance function, and for tetR, the Tn10 tet represser, are transcribed in opposite directions from promoters in a regulatory region located between the two structural genes. Expression of both tetA and tetR is induced by tetracycline. Here we report the DNA sequence of the Tn10 tet regulatory region. The locations of the tetA and tetR promoters within this region were defined by S1 nuclease mapping of the 5′ ends of in vivo tet RNA. The tetA and tetR promoters overlap; the transcription start points are separated by 36 bp. We propose that two similar regions of dyad symmetry within the Tn10 tet regulatory region are operator sites at which tet repressor binds to tet DNA, thereby inhibiting transcription initiation at the tetA and tetR promoters. The Tn10 tet regulatory region and the pBR322 tet regulatory region show significant DNA sequence homology (53%).
AB - We have previously examined the genetic organization and regulation of the Tn10 tetracycline-resistance determinant in Escherichia coli K-12. The structural genes for tetA, the Tn10 tetracycline-resistance function, and for tetR, the Tn10 tet represser, are transcribed in opposite directions from promoters in a regulatory region located between the two structural genes. Expression of both tetA and tetR is induced by tetracycline. Here we report the DNA sequence of the Tn10 tet regulatory region. The locations of the tetA and tetR promoters within this region were defined by S1 nuclease mapping of the 5′ ends of in vivo tet RNA. The tetA and tetR promoters overlap; the transcription start points are separated by 36 bp. We propose that two similar regions of dyad symmetry within the Tn10 tet regulatory region are operator sites at which tet repressor binds to tet DNA, thereby inhibiting transcription initiation at the tetA and tetR promoters. The Tn10 tet regulatory region and the pBR322 tet regulatory region show significant DNA sequence homology (53%).
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U2 - 10.1016/0378-1119(83)90046-X
DO - 10.1016/0378-1119(83)90046-X
M3 - Article
C2 - 6311683
AN - SCOPUS:0020595444
SN - 0378-1119
VL - 23
SP - 149
EP - 156
JO - Gene
JF - Gene
IS - 2
ER -