IscR-dependent gene expression links iron-sulphur cluster assembly to the control of O2-regulated genes in Escherichia coli

被引:214
作者
Giel, JL
Rodionov, D
Liu, MZ
Blattner, FR
Kiley, PJ [1 ]
机构
[1] Univ Wisconsin, Dept Biomol Chem, Madison, WI 53706 USA
[2] Univ Wisconsin, Microbiol Doctoral Training Program, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
[4] Russian Acad Sci, Inst Informat Transmiss Problems, Moscow 127994, Russia
关键词
D O I
10.1111/j.1365-2958.2006.05160.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
IscR is an iron-sulphur (Fe-S) cluster-containing transcription factor that represses transcription of the operon containing its own gene and the iscSUA-hscBA-fdx genes, whose products are involved in Fe-S cluster biogenesis. In this study, global transcriptional profiling of Escherichia coli IscR(+) and IscR(-) strains grown under aerobic and anaerobic conditions indicated that 40 genes in 20 predicted operons were regulated by IscR. DNase I footprinting and/or in vitro transcription reactions identified seven new promoters under direct IscR control. Among these were genes encoding known or proposed functions in Fe-S cluster biogenesis (sufABCDSE, yadR and yhgI) and Fe-S cluster-containing anaerobic respiratory enzymes (hyaABCDEF, hybOABCDEFG and napFDAGHBC). The finding that IscR repressed expression of the hyaA, hybO and napF promoters specifically under aerobic growth conditions suggests a new mechanism to explain their upregulation under anaerobic growth conditions. Phylogenetic footprinting of the DNase I protected regions of seven promoters implies that there are at least two different classes of IscR binding sites conserved among many bacteria. The findings presented here indicate a more general role of IscR in the regulation of Fe-S cluster biogenesis and that IscR contributes to the O-2 regulation of several promoters controlling the expression of anaerobic Fe-S proteins.
引用
收藏
页码:1058 / 1075
页数:18
相关论文
共 64 条
[1]   IscU as a scaffold for iron-sulfur cluster biosynthesis: Sequential assembly of [2Fe-2S] and [4Fe-4S] clusters in IscU [J].
Agar, JN ;
Krebs, C ;
Frazzon, J ;
Huynh, BH ;
Dean, DR ;
Johnson, MK .
BIOCHEMISTRY, 2000, 39 (27) :7856-7862
[2]   Predicting bacterial transcription units using sequence and expression data [J].
Bockhorst, Joseph ;
Qiu, Yu ;
Glasner, Jeremy ;
Liu, Mingzhu ;
Blattner, Frederick ;
Craven, Mark .
BIOINFORMATICS, 2003, 19 :i34-i43
[3]  
BRONDSTED L, 1994, J BACTERIOL, V176, P5423
[4]   Interaction network containing conserved and essential protein complexes in Escherichia coli [J].
Butland, G ;
Peregrín-Alvarez, JM ;
Li, J ;
Yang, WH ;
Yang, XC ;
Canadien, V ;
Starostine, A ;
Richards, D ;
Beattie, B ;
Krogan, N ;
Davey, M ;
Parkinson, J ;
Greenblatt, J ;
Emili, A .
NATURE, 2005, 433 (7025) :531-537
[5]   Multiple sequence alignment with the Clustal series of programs [J].
Chenna, R ;
Sugawara, H ;
Koike, T ;
Lopez, R ;
Gibson, TJ ;
Higgins, DG ;
Thompson, JD .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3497-3500
[6]   IDENTIFICATION OF THE REGULATORY SEQUENCE OF ANAEROBICALLY EXPRESSED LOCUS AEG-46.5 [J].
CHOE, M ;
REZNIKOFF, WS .
JOURNAL OF BACTERIOLOGY, 1993, 175 (04) :1165-1172
[7]   ANAEROBICALLY EXPRESSED ESCHERICHIA-COLI GENES IDENTIFIED BY OPERON FUSION TECHNIQUES [J].
CHOE, M ;
REZNIKOFF, WS .
JOURNAL OF BACTERIOLOGY, 1991, 173 (19) :6139-6146
[8]   INTERACTION OF 6 GLOBAL TRANSCRIPTION REGULATORS IN EXPRESSION OF MANGANESE SUPEROXIDE-DISMUTASE IN ESCHERICHIA-COLI K-12 [J].
COMPAN, I ;
TOUATI, D .
JOURNAL OF BACTERIOLOGY, 1993, 175 (06) :1687-1696
[9]   WebLogo: A sequence logo generator [J].
Crooks, GE ;
Hon, G ;
Chandonia, JM ;
Brenner, SE .
GENOME RESEARCH, 2004, 14 (06) :1188-1190
[10]   NITRATE AND NITRITE REGULATION OF THE FNR-DEPENDENT AEG-46.5 PROMOTER OF ESCHERICHIA-COLI K-12 IS MEDIATED BY COMPETITION BETWEEN HOMOLOGOUS RESPONSE REGULATORS (NARL AND NARP) FOR A COMMON DNA-BINDING SITE [J].
DARWIN, AJ ;
STEWART, V .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 251 (01) :15-29