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硫氧还蛋白-2通过还原SqrR中的多硫化物连接来调节SqrR介导的多硫化物响应转录。

Thioredoxin-2 Regulates SqrR-Mediated Polysulfide-Responsive Transcription via Reduction of a Polysulfide Link in SqrR.

作者信息

Shimizu Takayuki, Hashimoto Masaru, Masuda Tatsuru

机构信息

Graduate School of Arts and Sciences, The University of Tokyo, Tokyo 153-8902, Japan.

出版信息

Antioxidants (Basel). 2023 Mar 11;12(3):699. doi: 10.3390/antiox12030699.

Abstract

Polysulfide plays an essential role in controlling various physiological activities in almost all organisms. We recently investigated the impact of polysulfide metabolic enzymes on the temporal dynamics of cellular polysulfide speciation and transcriptional regulation by the polysulfide-responsive transcription factor SqrR in . However, how the polysulfidation of thiol groups in SqrR is reduced remains unclear. In the present study, we examined the reduction of polysulfidated thiol residues by the thioredoxin system. TrxC interacted with SqrR in vitro and reduced the polysulfide crosslink between two cysteine residues in SqrR. Furthermore, we found that exogenous sulfide-induced SqrR de-repression during longer culture times is maintained upon disruption of the gene. These results establish a novel signaling pathway in SqrR-mediated polysulfide-induced transcription, by which thioredoxin-2 restores SqrR to a transcriptionally repressed state via the reduction of polysulfidated thiol residues.

摘要

多硫化物在几乎所有生物体中控制各种生理活动方面发挥着重要作用。我们最近研究了多硫化物代谢酶对细胞多硫化物形态的时间动态以及多硫化物反应转录因子SqrR在[具体生物]中的转录调控的影响。然而,SqrR中硫醇基团的多硫化作用如何被还原仍不清楚。在本研究中,我们研究了硫氧还蛋白系统对多硫化硫醇残基的还原作用。TrxC在体外与SqrR相互作用,并减少了SqrR中两个半胱氨酸残基之间的多硫化物交联。此外,我们发现,在较长培养时间内,外源性硫化物诱导的SqrR去抑制在[具体基因]被破坏后仍得以维持。这些结果在SqrR介导的多硫化物诱导转录中建立了一条新的信号通路,通过该通路硫氧还蛋白-2通过还原多硫化硫醇残基将SqrR恢复到转录抑制状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e9c/10044876/b2b31d1d50d6/antioxidants-12-00699-g004.jpg

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