Expression of the cold-shock gene cspB in Salmonella typhimurium occurs below a threshold temperature

被引:23
作者
Craig, JE [1 ]
Boyle, D [1 ]
Francis, KP [1 ]
Gallagher, MP [1 ]
机构
[1] Univ Edinburgh, Inst Cell & Mol Biol, Div Biol, Edinburgh EH9 3JR, Midlothian, Scotland
来源
MICROBIOLOGY-UK | 1998年 / 144卷
关键词
bioluminescence; cold shock; CspB; temperature threshold; Salmonella typhimurium;
D O I
10.1099/00221287-144-3-697
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Previous studies have shown that several bacterial species exhibit a multigenic response following temperature downshift (cold shock). Evidence for such a response in Salmonella typhimurium is reported, based on the isolation of a range of low-induction-temperature gene fusions containing Mudlux insertions. The fusions exhibited different levels of basal light at 30 degrees C, and were induced at different rates and to different degrees over several hours following a reduction in temperature to 10 degrees C. Of the Mudlux gene fusions isolated, one was found which produced essentially no light when grown at 30 degrees C but exhibited rapid and high-level induction when the temperature was reduced to 10 degrees C. The target of this gene fusion (which was named cspB) was shown to lie adjacent to the umuDC operon and to encode a homologue of the major cold-shock protein of Escherichia coli, CspA. Luminescence studies revealed that substantial light production occurred from the cspB::Mudlux fusion at or below 22 degrees C but not at higher temperatures, even following a temperature drop from 30 degrees C. Moreover, cspB mRNA levels were found to mimic this pattern of luminescence, suggesting that cspB expression occurs below a defined temperature threshold. The cspB mRNA was also found to be very stable at 10 degrees C but to become highly unstable when the temperature was raised towards the threshold temperature, even in the presence of rifampicin. Existing cellular RNases therefore appear to mediate the decay of cspB mRNA at high temperatures, but are incapable of this at low temperatures.
引用
收藏
页码:697 / 704
页数:8
相关论文
共 37 条
[1]  
Ausubel F.M., 1992, CURRENT PROTOCOLS MO
[2]   STREPTOMYCES CONTAIN A 7.0 KDA COLD SHOCK LIKE PROTEIN [J].
AVGAY, Y ;
AHARONOWITZ, Y ;
COHEN, G .
NUCLEIC ACIDS RESEARCH, 1992, 20 (20) :5478-5478
[3]   RAPID MAPPING IN SALMONELLA-TYPHIMURIUM WITH MUD-P22 PROPHAGES [J].
BENSON, NR ;
GOLDMAN, BS .
JOURNAL OF BACTERIOLOGY, 1992, 174 (05) :1673-1681
[4]   Post-transcriptional regulation of CspA expression in Escherichia coli [J].
Brandi, A ;
Pietroni, P ;
Gualerzi, CO ;
Pon, CL .
MOLECULAR MICROBIOLOGY, 1996, 19 (02) :231-240
[5]   Differential thermoregulation of two highly homologous cold-shock genes, cspA and cspB, of Escherichia coli [J].
Etchegaray, JP ;
Jones, PG ;
Inouye, M .
GENES TO CELLS, 1996, 1 (02) :171-178
[6]   Promoter-independent cold-shock induction of cspA and its derepression at 37 degrees C by mRNA stabilization [J].
Fang, L ;
Jiang, WN ;
Bae, WH ;
Inouye, M .
MOLECULAR MICROBIOLOGY, 1997, 23 (02) :355-364
[7]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[8]  
FEINBERG AP, 1984, ANAL BIOCHEM, V137, P266
[9]   LIGHT-EMISSION FROM A MUDLUX TRANSCRIPTIONAL FUSION IN SALMONELLA-TYPHIMURIUM IS STIMULATED BY HYDROGEN-PEROXIDE AND BY INTERACTION WITH THE MOUSE MACROPHAGE CELL-LINE J774.2 [J].
FRANCIS, KP ;
GALLAGHER, MP .
INFECTION AND IMMUNITY, 1993, 61 (02) :640-649
[10]   Differential mRNA stability of the cspA gene in the cold-shock response of Escherichia coli [J].
Goldenberg, D ;
Azar, I ;
Oppenheim, AB .
MOLECULAR MICROBIOLOGY, 1996, 19 (02) :241-248