IRON, DTXR, AND THE REGULATION OF DIPHTHERIA-TOXIN EXPRESSION

被引:112
作者
TAO, X
SCHIERING, N
ZENG, HY
RINGE, D
MURPHY, JR
机构
[1] BOSTON UNIV, MED CTR HOSP, EVANS DEPT CLIN RES, BOSTON, MA 02118 USA
[2] BOSTON UNIV, MED CTR HOSP, DEPT MED, BOSTON, MA 02118 USA
[3] BRANDEIS UNIV, DEPT BIOCHEM, WALTHAM, MA 02254 USA
[4] BRANDEIS UNIV, DEPT CHEM, WALTHAM, MA 02254 USA
关键词
D O I
10.1111/j.1365-2958.1994.tb01280.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
In recent years considerable advances have been made in the understanding of the molecular basis of iron-mediated regulation of diphtheria toxin expression. The fox gene has been shown to be regulated by the heavy metal ion-activated regulatory element DtxR. In the presence of divalent heavy metal ions, DtxR becomes activated and binds to a 9 bp interrupted palindromic sequence. The consensus-binding site has been determined by both the sequence analysis of DtxR-responsive operators cloned from genomic libraries of Corynebacterium diphtheriae as well as by in vitro genetic methods using cyclic amplification of selected targets (CASTing). It Is now clear that DtxR functions as a global iron-sensitive regulatory element in the control of gene expression in C. diphtheriae. In addition, the metal ion-activation domain of DtxR is being characterized by both mutational analysis and determination of the X-ray structure at 3.0 Angstrom resolution.
引用
收藏
页码:191 / 197
页数:7
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