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感知铁的可用性:细菌转录阻遏物RirA的脆弱[4Fe-4S]簇

Sensing iron availability the fragile [4Fe-4S] cluster of the bacterial transcriptional repressor RirA.

作者信息

Pellicer Martinez Ma Teresa, Martinez Ana Bermejo, Crack Jason C, Holmes John D, Svistunenko Dimitri A, Johnston Andrew W B, Cheesman Myles R, Todd Jonathan D, Le Brun Nick E

机构信息

Centre for Molecular and Structural Biochemistry , School of Chemistry , University of East Anglia , Norwich Research Park , Norwich , NR4 7TJ , UK . Email:

School of Biological Sciences , University of East Anglia , Norwich Research Park , Norwich , NR4 7TJ , UK.

出版信息

Chem Sci. 2017 Dec 1;8(12):8451-8463. doi: 10.1039/c7sc02801f. Epub 2017 Oct 23.

DOI:10.1039/c7sc02801f
PMID:29619193
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5863699/
Abstract

Rhizobial iron regulator A (RirA) is a global regulator of iron homeostasis in many nitrogen-fixing Rhizobia and related species of α-proteobacteria. It belongs to the widespread Rrf2 super-family of transcriptional regulators and features three conserved Cys residues that characterise the binding of an iron-sulfur cluster in other Rrf2 family regulators. Here we report biophysical studies demonstrating that RirA contains a [4Fe-4S] cluster, and that this form of the protein binds RirA-regulated DNA, consistent with its function as a repressor of expression of many genes involved in iron uptake. Under low iron conditions, [4Fe-4S] RirA undergoes a cluster conversion reaction resulting in a [2Fe-2S] form, which exhibits much lower affinity for DNA. Under prolonged low iron conditions, the [2Fe-2S] cluster degrades to apo-RirA, which does not bind DNA and can no longer function as a repressor of the cell's iron-uptake machinery. [4Fe-4S] RirA was also found to be sensitive to O, suggesting that both iron and O are important signals for iron metabolism. Consistent with this, data showed that expression of RirA-regulated genes is also affected by O. These data lead us to propose a novel regulatory model for iron homeostasis, in which RirA senses iron the incorporation of a fragile iron-sulfur cluster that is sensitive to iron and O concentrations.

摘要

根瘤菌铁调节蛋白A(RirA)是许多固氮根瘤菌及相关α-变形杆菌中铁稳态的全局调节因子。它属于广泛存在的转录调节因子Rrf2超家族,具有三个保守的半胱氨酸残基,这些残基是其他Rrf2家族调节因子中结合铁硫簇的特征。在此,我们报告的生物物理研究表明,RirA含有一个[4Fe-4S]簇,并且这种形式的蛋白质结合受RirA调节的DNA,这与其作为许多参与铁摄取的基因表达阻遏物的功能一致。在低铁条件下,[4Fe-4S] RirA会发生簇转化反应,生成[2Fe-2S]形式,其对DNA的亲和力要低得多。在长期低铁条件下,[2Fe-2S]簇会降解为脱辅基RirA,后者不结合DNA,并且不再能作为细胞铁摄取机制的阻遏物发挥作用。还发现[4Fe-4S] RirA对氧气敏感,这表明铁和氧气都是铁代谢的重要信号。与此一致的是,数据显示受RirA调节的基因表达也受氧气影响。这些数据使我们提出了一种新的铁稳态调节模型,其中RirA通过一个对铁和氧气浓度敏感的脆弱铁硫簇的掺入来感知铁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/41d77c1b6572/c7sc02801f-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/63fd8e6844e5/c7sc02801f-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/139545da783c/c7sc02801f-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/b8f5b4572463/c7sc02801f-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/81142d113aca/c7sc02801f-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/41d77c1b6572/c7sc02801f-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/63fd8e6844e5/c7sc02801f-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/a48e8e4b555e/c7sc02801f-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/ca94e37e461b/c7sc02801f-f3.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/139545da783c/c7sc02801f-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/b8f5b4572463/c7sc02801f-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/81142d113aca/c7sc02801f-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1756/5863699/41d77c1b6572/c7sc02801f-f8.jpg

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