Discovery of Fur binding site clusters in Escherichia coli by information theory models

被引:73
作者
Chen, Zehua
Lewis, Karen A.
Shultzaberger, Ryan K.
Lyakhov, Ilya G.
Zheng, Ming
Doan, Bernard
Storz, Gisela
Schneider, Thomas D. [1 ]
机构
[1] NCI, Ctr Canc Res Nanobiol Program, Ft Detrick, MD 21702 USA
[2] NCI, Basic Res Program, SAIC Frederick Inc, Ft Detrick, MD 21702 USA
[3] NICHHD, Cell Biol & Metab Branch, Bethesda, MD 20892 USA
[4] NIAID, Referral & Program Anal Branch, Div Extramural Activities, Bethesda, MD 20892 USA
关键词
D O I
10.1093/nar/gkm631
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
Fur is a DNA binding protein that represses bacterial iron uptake systems. Eleven footprinted Escherichia coli Fur binding sites were used to create an initial information theory model of Fur binding, which was then refined by adding 13 experimentally confirmed sites. When the refined model was scanned across all available footprinted sequences, sequence walkers, which are visual depictions of predicted binding sites, frequently appeared in clusters that fit the footprints (83 coverage). This indicated that the model can accurately predict Fur binding. Within the clusters, individual walkers were separated from their neighbors by exactly 3 or 6 bases, consistent with models in which Fur dimers bind on different faces of the DNA helix. When the E. coli genome was scanned, we found 363 unique clusters, which includes all known Fur-repressed genes that are involved in iron metabolism. In contrast, only a few of the known Fur-activated genes have predicted Fur binding sites at their promoters. These observations suggest that Fur is either a direct repressor or an indirect activator. The Pseudomonas aeruginosa and Bacillus subtilis Fur models are highly similar to the E. coli Fur model, suggesting that the FurDNA recognition mechanism may be conserved for even distantly related bacteria.
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收藏
页码:6762 / 6777
页数:16
相关论文
共 85 条
[1]   The ferric uptake regulation (Fur) repressor is a zinc metalloprotein [J].
Althaus, EW ;
Outten, CE ;
Olson, KE ;
Cao, H ;
O'Halloran, TV .
BIOCHEMISTRY, 1999, 38 (20) :6559-6569
[2]   Bacterial iron homeostasis [J].
Andrews, SC ;
Robinson, AK ;
Rodríguez-Quiñones, F .
FEMS MICROBIOLOGY REVIEWS, 2003, 27 (2-3) :215-237
[3]   Iron regulates transcription of the Escherichia coli ferric citrate transport genes directly and through the transcription initiation proteins [J].
Angerer, A ;
Braun, V .
ARCHIVES OF MICROBIOLOGY, 1998, 169 (06) :483-490
[4]  
[Anonymous], 1980, An Introduction to Information Theory
[5]   Novel small RNA-encoding genes in the intergenic regions of Escherichia coli [J].
Argaman, L ;
Hershberg, R ;
Vogel, J ;
Bejerano, G ;
Wagner, EGH ;
Margalit, H ;
Altuvia, S .
CURRENT BIOLOGY, 2001, 11 (12) :941-950
[6]   FERRIC UPTAKE REGULATION PROTEIN ACTS AS A REPRESSOR, EMPLOYING IRON(II) AS A COFACTOR TO BIND THE OPERATOR OF AN IRON TRANSPORT OPERON IN ESCHERICHIA-COLI [J].
BAGG, A ;
NEILANDS, JB .
BIOCHEMISTRY, 1987, 26 (17) :5471-5477
[7]   MOLECULAR MECHANISM OF REGULATION OF SIDEROPHORE-MEDIATED IRON ASSIMILATION [J].
BAGG, A ;
NEILANDS, JB .
MICROBIOLOGICAL REVIEWS, 1987, 51 (04) :509-518
[8]   Recognition of DNA by Fur: a reinterpretation of the Fur box consensus sequence [J].
Baichoo, N ;
Helmann, JD .
JOURNAL OF BACTERIOLOGY, 2002, 184 (21) :5826-5832
[9]   Global analysis of the Bacillus subtilis Fur regulon and the iron starvation stimulon [J].
Baichoo, N ;
Wang, T ;
Ye, R ;
Helmann, JD .
MOLECULAR MICROBIOLOGY, 2002, 45 (06) :1613-1629
[10]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+