Identification and characterization of a regulatory sequence recognized by Mycobacterium tuberculosis persistence regulator MprA

被引:65
作者
He, HJ [1 ]
Zahrt, TC [1 ]
机构
[1] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
关键词
D O I
10.1128/JB.187.1.202-212.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Establishment and maintenance of persistent, latent infection by Mycobacterium tuberculosis are dependent on expression of the mprA-mprB regulatory system. Previously, MprA and MprB were shown to participate in phosphotransfer reactions characteristic of two-component signaling systems. To begin identifying downstream effector genes regulated by mprA-mprB during persistent stages of infection, a search for the regulatory sequence(s) recognized by response regulator MprA was carried out. Here, evidence is presented demonstrating that MprA recognizes a 19-bp sequence comprising two loosely conserved 8-bp direct repeat subunits separated by 3 nucleotides. This motif, termed the MprA box, is found upstream of the mprA coding sequence and that of downstream gene pepD (Rv0983). Protein phosphorylation was not required for binding to this DNA sequence by MprA in vitro; however, phosphorylation enhanced DNA binding by MprA and was required for the regulation of mprA and pepD by MprA in vivo. Binding of MprA to the MprA box was dependent on conserved nucleotides contained within repeat subunits and on the spacer length separating these repeats. In addition, recognition of this sequence proceeded via tandem binding of two monomers of MprA. Identification of the genetic determinants regulated by MprA will ultimately enhance our understanding of the mechanisms utilized by M. tuberculosis to undergo latency.
引用
收藏
页码:202 / 212
页数:11
相关论文
共 45 条
[1]   The pandemic of antibiotic resistance [J].
Anderson, RM .
NATURE MEDICINE, 1999, 5 (02) :147-149
[2]   The evolving relation between humans and Mycobacterium tuberculosis [J].
Bloom, BR ;
Small, PM .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (10) :677-678
[3]   TUBERCULOSIS - COMMENTARY ON A REEMERGENT KILLER [J].
BLOOM, BR ;
MURRAY, CJL .
SCIENCE, 1992, 257 (5073) :1055-1064
[4]   SYNERGISTIC BINDING OF RNA-POLYMERASE AND BVGA PHOSPHATE TO THE PERTUSSIS TOXIN PROMOTER OF BORDETELLA-PERTUSSIS [J].
BOUCHER, PE ;
STIBITZ, S .
JOURNAL OF BACTERIOLOGY, 1995, 177 (22) :6486-6491
[5]   The HtrA family of proteases: Implications for protein composition and cell fate [J].
Clausen, T ;
Southan, C ;
Ehrmann, M .
MOLECULAR CELL, 2002, 10 (03) :443-455
[6]   Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence [J].
Cole, ST ;
Brosch, R ;
Parkhill, J ;
Garnier, T ;
Churcher, C ;
Harris, D ;
Gordon, SV ;
Eiglmeier, K ;
Gas, S ;
Barry, CE ;
Tekaia, F ;
Badcock, K ;
Basham, D ;
Brown, D ;
Chillingworth, T ;
Connor, R ;
Davies, R ;
Devlin, K ;
Feltwell, T ;
Gentles, S ;
Hamlin, N ;
Holroyd, S ;
Hornby, T ;
Jagels, K ;
Krogh, A ;
McLean, J ;
Moule, S ;
Murphy, L ;
Oliver, K ;
Osborne, J ;
Quail, MA ;
Rajandream, MA ;
Rogers, J ;
Rutter, S ;
Seeger, K ;
Skelton, J ;
Squares, R ;
Squares, S ;
Sulston, JE ;
Taylor, K ;
Whitehead, S ;
Barrell, BG .
NATURE, 1998, 393 (6685) :537-+
[7]   Role of the htrA gene in Klebsiella pneumoniae virulence [J].
Cortés, G ;
de Astorza, B ;
Benedí, VJ ;
Albertí, S .
INFECTION AND IMMUNITY, 2002, 70 (09) :4772-4776
[8]   Characterization of a two component system, devR-devS, of Mycobacterium tuberculosis [J].
Dasgupta, N ;
Kapur, V ;
Singh, KK ;
Das, TK ;
Sachdeva, S ;
Jyothisri, K ;
Tyagi, JS .
TUBERCLE AND LUNG DISEASE, 2000, 80 (03) :141-159
[9]   Global burden of tuberculosis - Estimated incidence, prevalence, and mortality by country [J].
Dye, C ;
Scheele, S ;
Dolin, P ;
Pathania, V ;
Raviglione, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 282 (07) :677-686
[10]   Microarray analysis of the Mycobacterium tuberculosis transcriptional response to the acidic conditions found in phagosomes [J].
Fisher, MA ;
Plikaytis, BB ;
Shinnick, TM .
JOURNAL OF BACTERIOLOGY, 2002, 184 (14) :4025-4032