An SmtB-like repressor from Synechocystis PCC 6803 regulates a zinc exporter

被引:140
作者
Thelwell, C [1 ]
Robinson, NJ [1 ]
Turner-Cavet, JS [1 ]
机构
[1] Newcastle Univ, Sch Med, Dept Biochem & Genet, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
D O I
10.1073/pnas.95.18.10728
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ORF slr0798, now designated ziaA, from Synechocystis PCC 6803 encodes a polypeptide with sequence features of heavy metal transporting P-type ATPases, Increased Zn2+ tolerance and reduced Zn-65 accumulation was observed in Synechococcus PCC 7942, strain R2-PIM8(smt), containing ziaA and upstream regulatory sequences, compared with control cells. Conversely, reduced Zn2+ tolerance was observed following disruption of ziaA in Synechocystis PCC 6803, and ziaA-mediated restoration of Zn2+ tolerance has subsequently been used as a selectable marker for transformation. Nucleotide sequences upstream of ziaA, fused to a promoterless lacZ gene, conferred Zn2+-dependent beta-galactosidase activity when introduced into R2-PIM8(smt). The product of ORF sll0792, designated ZiaR, is a Zn2+-responsive repressor of ziaA transcription. Reporter gene constructs lacking ziaR conferred elevated Zn2+-independent expression from the ziaA operator-promoter in R2-PIM8(smt), Gel retardation assays detected ZiaR-dependent complexes forming with the zia operator-promoter and ZiaR-DNA binding was enhanced by treatment with a metal-chelator in vitro. Two mutants of ZiaR (C71S/C73S and H116R) bound to, and repressed expression from, the ziaA operator-promoter hut were unable to sense Zn2+, Metal coordination to His-imidazole and Cys-thiolate ligands at these residues of ZiaR is thus implicated in Zn2+-perception by Synechocystis PCC 6803.
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页码:10728 / 10733
页数:6
相关论文
共 27 条
[1]   Zinc(II) tolerance in Escherichia coli K-12: evidence that the zntA gene (o732) encodes a cation transport ATPase [J].
Beard, SJ ;
Hashim, R ;
MembrilloHernandez, J ;
Hughes, MN ;
Poole, RK .
MOLECULAR MICROBIOLOGY, 1997, 25 (05) :883-891
[2]  
Blencowe D. K., 1997, BIOTECHNOLOGY ELIA, V2, P1
[3]   Crystal structure of the cyanobacterial metallothionein repressor SmtB: A model for metalloregulatory proteins [J].
Cook, WJ ;
Kar, SR ;
Taylor, KB ;
Hall, LM .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (02) :337-346
[4]   Expression, purification, and metal binding properties of the N-terminal domain from the Wilson disease putative copper-transporting ATPase (ATP7B) [J].
DiDonato, M ;
Narindrasorasak, S ;
Forbes, JR ;
Cox, DW ;
Sarkar, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (52) :33279-33282
[5]   CADC, THE TRANSCRIPTIONAL REGULATORY PROTEIN OF THE CADMIUM RESISTANCE SYSTEM OF STAPHYLOCOCCUS-AUREUS PLASMID PI258 [J].
ENDO, G ;
SILVER, S .
JOURNAL OF BACTERIOLOGY, 1995, 177 (15) :4437-4441
[6]   METALLOREGULATION OF THE CYANOBACTERIAL SMT LOCUS - IDENTIFICATION OF SMTB BINDING-SITES AND DIRECT INTERACTION WITH METALS [J].
ERBE, JL ;
TAYLOR, KB ;
HALL, LM .
NUCLEIC ACIDS RESEARCH, 1995, 23 (13) :2472-2478
[7]   SEQUENCE, MAPPING AND DISRUPTION OF CCC2, A GENE THAT CROSS-COMPLEMENTS THE CA2+-SENSITIVE PHENOTYPE OF CSG1 MUTANTS AND ENCODES A P-TYPE ATPASE BELONGING TO THE CU2+-ATPASE SUBFAMILY [J].
FU, DD ;
BEELER, TJ ;
DUNN, TM .
YEAST, 1995, 11 (03) :283-292
[8]   ISOLATION OF A PROKARYOTIC METALLOTHIONEIN LOCUS AND ANALYSIS OF TRANSCRIPTIONAL CONTROL BY TRACE-METAL IONS [J].
HUCKLE, JW ;
MORBY, AP ;
TURNER, JS ;
ROBINSON, NJ .
MOLECULAR MICROBIOLOGY, 1993, 7 (02) :177-187
[9]   A COPPER-TRANSPORTING P-TYPE ATPASE FOUND IN THE THYLAKOID MEMBRANE OF THE CYANOBACTERIUM SYNECHOCOCCUS SPECIES PCC7942 [J].
KANAMARU, K ;
KASHIWAGI, S ;
MIZUNO, T .
MOLECULAR MICROBIOLOGY, 1994, 13 (02) :369-377
[10]  
Kaneko T, 1996, DNA Res, V3, P109