Developmental switch of S-layer protein synthesis in Bacillus anthracis

被引:81
作者
Mignot, T
Mesnage, S
Couture-Tosi, E
Mock, M
Fouet, A
机构
[1] Inst Pasteur, CNRS, URA 2172, F-75724 Paris 15, France
[2] Inst Pasteur, CNRS, URA 2185, Grp Microscopie Struct Mol, F-75724 Paris, France
关键词
D O I
10.1046/j.1365-2958.2002.02852.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adjustment of the synthesis of abundant protein to the requirements of the cell involves processes critical to the minimization of energy expenditure. The regulation of S-layer genes might be a good model for such processes because expression must be controlled, such that the encoded proteins exactly cover the surface of the bacterium. Bacillus anthracis has two S-layer genes, sap and eag, encoding the S-layer proteins Sap and EA1 respectively. We report that the production and surface localization of Sap and EA1 are under developmental control, suggesting that an exponential phase 'Sap layer' is subsequently replaced by a stationary phase 'EA1 layer'. This switch is controlled at the transcriptional level: sap is most certainly transcribed by RNA polymerase containing sigma(A), whereas eag expression depends on sigma(H). More importantly, Sap is required for the temporal control of eag, and EA1 is involved in strict feedback regulation of eag. This control may be direct because both S-layer proteins bind, in vitro, the eag promoter, specifically suggesting that they might act as transcriptional repressors.
引用
收藏
页码:1615 / 1627
页数:13
相关论文
共 40 条
[1]   STAB-SD: A Shine-Dalgarno sequence in the 5' untranslated region is a determinant of mRNA stability [J].
Agaisse, H ;
Lereclus, D .
MOLECULAR MICROBIOLOGY, 1996, 20 (03) :633-643
[2]   PATHOGENESIS OF CAMPYLOBACTER-FETUS INFECTIONS - SERUM RESISTANCE ASSOCIATED WITH HIGH-MOLECULAR-WEIGHT SURFACE-PROTEINS [J].
BLASER, MJ ;
SMITH, PF ;
HOPKINS, JA ;
HEINZER, I ;
BRYNER, JH ;
WANG, WLL .
JOURNAL OF INFECTIOUS DISEASES, 1987, 155 (04) :696-706
[3]   The Lactobacillus acidophilus S-layer protein gene expression site comprises two consensus promoter sequences, one of which directs transcription of stable mRNA [J].
Boot, HJ ;
Kolen, CPAM ;
Andreadaki, FJ ;
Leer, RJ ;
Pouwels, PH .
JOURNAL OF BACTERIOLOGY, 1996, 178 (18) :5388-5394
[4]   Multiple regulatory mechanisms act on the 5′ untranslated region of the S-layer gene from Thermus thermophilus HB8 [J].
Castán, P ;
de Pedro, MA ;
Risco, C ;
Vallés, C ;
Fernández, LA ;
Schwarz, H ;
Berenguer, J .
JOURNAL OF BACTERIOLOGY, 2001, 183 (04) :1491-1494
[5]   Distinct affinity of binding sites for S-layer homologous domains in Clostridium thermocellum and Bacillus anthracis cell envelopes [J].
Chauvaux, S ;
Matuschek, M ;
Beguin, P .
JOURNAL OF BACTERIOLOGY, 1999, 181 (08) :2455-2458
[6]   AN AEROMONAS-SALMONICIDA GENE WHICH INFLUENCES A-PROTEIN EXPRESSION IN ESCHERICHIA-COLI ENCODES A PROTEIN CONTAINING AN ATP-BINDING CASSETTE AND MAPS BESIDE THE SURFACE ARRAY PROTEIN GENE [J].
CHU, S ;
TRUST, TJ .
JOURNAL OF BACTERIOLOGY, 1993, 175 (10) :3105-3114
[7]   TRANSCRIPTIONAL ANALYSIS OF THE AEROMONAS-SALMONICIDA S-LAYER PROTEIN GENE VAPA [J].
CHU, SJ ;
GUSTAFSON, CE ;
FEUTRIER, J ;
CAVAIGNAC, S ;
TRUST, TJ .
JOURNAL OF BACTERIOLOGY, 1993, 175 (24) :7968-7975
[8]   CtsR, a novel regulator of stress and heat shock response, controls clp and molecular chaperone gene expression in Gram-positive bacteria [J].
Derré, I ;
Rapoport, G ;
Msadek, T .
MOLECULAR MICROBIOLOGY, 1999, 31 (01) :117-131
[9]   RELATIONSHIP BETWEEN ACONITASE GENE-EXPRESSION AND SPORULATION IN BACILLUS-SUBTILIS [J].
DINGMAN, DW ;
ROSENKRANTZ, MS ;
SONENSHEIN, AL .
JOURNAL OF BACTERIOLOGY, 1987, 169 (07) :3068-3075
[10]   Nested DNA inversion of Campylobacter fetus S-layer genes is recA dependent [J].
Dworkin, J ;
Shedd, OL ;
Blaser, MJ .
JOURNAL OF BACTERIOLOGY, 1997, 179 (23) :7523-7529