AUTOGENOUS REGULATION OF THE BORDETELLA-PERTUSSIS BVGABC OPERON

被引:63
作者
ROY, CR
MILLER, JF
FALKOW, S
机构
[1] Department of Microbiology, Stanford University, Stanford
关键词
Coordinate regulation; Signal transduction; Transcriptional fusions; Two-component system; Virulence genes;
D O I
10.1073/pnas.87.10.3763
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The bvgABC operon of the bacterial pathogen Bordetella pertussis encodes a sensory transduction system that regulates the expression of several virulence genes in response to environmental stimuli. In this study we have examined the transcriptional regulation of the bvgABC operon. Transcriptional bvg::lacZYA fusions in Escherichia coli show that the bvgABC operon is autogenously activated. Autoactivation is Inhibited by the same environmental stimuli that result in the lack of expression of bvg-activated genes in B. pertussis. These observations were confirmed in B. pertussis using a chromosomal chloramphenicol acetyltransferase transcriptional fusion in bvgC. Transcriptional initiation sites upstream of bvgA were mapped by primer extension analysis in E. coli and B. pertussis. Two differentially regulated bvg promoters were identified. The bvgpi promoter is a positively autoregulated promoter located 90 base pairs upstream of bvgA. The bvgP2 promoter is located 141 base pairs upstream of bvgA and does not appear to require any positive regulatory factors for activity. These results suggest a model describing the regulatory events that take place upstream of the bvgABC operon.
引用
收藏
页码:3763 / 3767
页数:5
相关论文
共 26 条
[1]   SEQUENCES REQUIRED FOR EXPRESSION OF BORDETELLA-PERTUSSIS VIRULENCE FACTORS SHARE HOMOLOGY WITH PROKARYOTIC SIGNAL TRANSDUCTION PROTEINS [J].
ARICO, B ;
MILLER, JF ;
ROY, C ;
STIBITZ, S ;
MONACK, D ;
FALKOW, S ;
GROSS, R ;
RAPPUOLI, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6671-6675
[2]   PLASMIDS RELATED TO THE BROAD HOST RANGE VECTOR, PRK290, USEFUL FOR GENE CLONING AND FOR MONITORING GENE-EXPRESSION [J].
DITTA, G ;
SCHMIDHAUSER, T ;
YAKOBSON, E ;
LU, P ;
LIANG, XW ;
FINLAY, DR ;
GUINEY, D ;
HELINSKI, DR .
PLASMID, 1985, 13 (02) :149-153
[3]   HIGH-EFFICIENCY TRANSFORMATION OF ESCHERICHIA-COLI BY HIGH-VOLTAGE ELECTROPORATION [J].
DOWER, WJ ;
MILLER, JF ;
RAGSDALE, CW .
NUCLEIC ACIDS RESEARCH, 1988, 16 (13) :6127-6145
[4]   RECOMBINANT GENOMES WHICH EXPRESS CHLORAMPHENICOL ACETYLTRANSFERASE IN MAMMALIAN-CELLS [J].
GORMAN, CM ;
MOFFAT, LF ;
HOWARD, BH .
MOLECULAR AND CELLULAR BIOLOGY, 1982, 2 (09) :1044-1051
[5]  
HARTZ D, 1988, METHOD ENZYMOL, V164, P419
[6]   COMPILATION AND ANALYSIS OF ESCHERICHIA-COLI PROMOTER DNA-SEQUENCES [J].
HAWLEY, DK ;
MCCLURE, WR .
NUCLEIC ACIDS RESEARCH, 1983, 11 (08) :2237-2255
[7]   2 TRANS-ACTING REGULATORY GENES (VIR AND MOD) CONTROL ANTIGENIC MODULATION IN BORDETELLA-PERTUSSIS [J].
KNAPP, S ;
MEKALANOS, JJ .
JOURNAL OF BACTERIOLOGY, 1988, 170 (11) :5059-5066
[8]   IDENTIFICATION AND LOCATION OF L-GLYCERATE, AN UNUSUAL ACYL SUBSTITUENT IN GELLAN GUM [J].
KUO, MS ;
MORT, AJ ;
DELL, A .
CARBOHYDRATE RESEARCH, 1986, 156 :173-187
[9]  
LACY BW, 1960, J HYG, V58, P57
[10]  
Maniatis T., 1982, MOL CLONING