Nitrosative stress: Activation of the transcription factor OxyR

被引:293
作者
Hausladen, A
Privalle, CT
Keng, T
DeAngelo, J
Stamler, JS
机构
[1] DUKE UNIV, MED CTR, DEPT MED, DURHAM, NC 27710 USA
[2] DUKE UNIV, MED CTR, DEPT CELL BIOL, DURHAM, NC 27710 USA
[3] APEX BIOSCI INC, RES TRIANGLE PK, NC 27709 USA
关键词
D O I
10.1016/S0092-8674(00)80147-6
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
Hydrogen peroxide (H2O2) imposes an oxidative stress to Escherichia coli that is manifested by oxidation of glutathione and related redox-sensitive targets. OxyR is a thiol-containing transcriptional activator whose oxidation controls the expression of genes involved in H2O2 detoxification. Here we report that certain S-nitrosothiols (RSNOs) impose what we term a ''nitrosative stress'' to E. coli, evidenced by lowering of intracellular thiol and the transcriptional activation of OxyR by S-nitrosylation. This cellular and genetic response determines the metabolic fate of RSNOs and thereby contributes to bacterial rescue from stasis. Our studies reveal that signaling by S-nitrosylation can extend to the level of transcription and describe a metabolic pathway that constitutes an adaptation to nitrosative stress.
引用
收藏
页码:719 / 729
页数:11
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