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UV-light-driven prebiotic synthesis of iron-sulfur clusters.紫外光驱动的类生命合成铁硫簇。
Nat Chem. 2017 Dec;9(12):1229-1234. doi: 10.1038/nchem.2817. Epub 2017 Jul 10.
2
The R213G polymorphism in SOD3 protects against allergic airway inflammation.SOD3 中的 R213G 多态性可预防过敏气道炎症。
JCI Insight. 2017 Sep 7;2(17). doi: 10.1172/jci.insight.95072.
3
Timing and tempo of the Great Oxidation Event.大氧化事件的时间和节奏。
Proc Natl Acad Sci U S A. 2017 Feb 21;114(8):1811-1816. doi: 10.1073/pnas.1608824114. Epub 2017 Feb 6.
4
Superoxide Dismutase 3 R213G Single-Nucleotide Polymorphism Blocks Murine Bleomycin-Induced Fibrosis and Promotes Resolution of Inflammation.超氧化物歧化酶3 R213G单核苷酸多态性可阻止小鼠博来霉素诱导的纤维化并促进炎症消退。
Am J Respir Cell Mol Biol. 2017 Mar;56(3):362-371. doi: 10.1165/rcmb.2016-0153OC.
5
The evolution of reactive oxygen species metabolism.活性氧代谢的演变。
J Exp Bot. 2016 Nov;67(21):5933-5943. doi: 10.1093/jxb/erw382. Epub 2016 Oct 14.
6
Oxidative stress and antioxidants: Distress or eustress?氧化应激与抗氧化剂:逆境还是良性应激?
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7
Lack of EC-SOD worsens alveolar and vascular development in a neonatal mouse model of bleomycin-induced bronchopulmonary dysplasia and pulmonary hypertension.在博来霉素诱导的支气管肺发育不良和肺动脉高压新生小鼠模型中,细胞外超氧化物歧化酶(EC-SOD)的缺乏会使肺泡和血管发育恶化。
Pediatr Res. 2015 Dec;78(6):634-40. doi: 10.1038/pr.2015.166. Epub 2015 Aug 31.
8
Extracellular Superoxide Dismutase Protects against Proteinuric Kidney Disease.细胞外超氧化物歧化酶可预防蛋白尿性肾病。
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9
Loss of SOD3 (EcSOD) Expression Promotes an Aggressive Phenotype in Human Pancreatic Ductal Adenocarcinoma.超氧化物歧化酶3(细胞外超氧化物歧化酶)表达缺失促进人胰腺导管腺癌的侵袭性表型。
Clin Cancer Res. 2015 Apr 1;21(7):1741-51. doi: 10.1158/1078-0432.CCR-14-1959. Epub 2015 Jan 29.
10
A common polymorphism in extracellular superoxide dismutase affects cardiopulmonary disease risk by altering protein distribution.细胞外超氧化物歧化酶中的一种常见多态性通过改变蛋白质分布影响心肺疾病风险。
Circ Cardiovasc Genet. 2014 Oct;7(5):659-66. doi: 10.1161/CIRCGENETICS.113.000504. Epub 2014 Aug 1.

超氧化物歧化酶的起源:超氧化物介导的氧化还原信号传导的进化视角

On the Origin of Superoxide Dismutase: An Evolutionary Perspective of Superoxide-Mediated Redox Signaling.

作者信息

Case Adam J

机构信息

Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, 985850 Nebraska Medical Center, Omaha, NE 68198, USA.

出版信息

Antioxidants (Basel). 2017 Oct 30;6(4):82. doi: 10.3390/antiox6040082.

DOI:10.3390/antiox6040082
PMID:29084153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5745492/
Abstract

The field of free radical biology originated with the discovery of superoxide dismutase (SOD) in 1969. Over the last 5 decades, a plethora of research has been performed in species ranging from bacteria to mammals that has elucidated the molecular reaction, subcellular location, and specific isoforms of SOD. However, while humans have only begun to study this class of enzymes over the past 50 years, it has been estimated that these enzymes have existed for billions of years, and may be some of the original enzymes found in primitive life. As life evolved over this expanse of time, these enzymes have taken on new and different functional roles potentially in contrast to how they were originally derived. Herein, examination of the evolutionary history of these enzymes provides both an explanation and further inquiries into the modern-day role of SOD in physiology and disease.

摘要

自由基生物学领域起源于1969年超氧化物歧化酶(SOD)的发现。在过去的50年里,针对从细菌到哺乳动物等物种开展了大量研究,阐明了SOD的分子反应、亚细胞定位和特定同工型。然而,尽管人类在过去50年才开始研究这类酶,但据估计这些酶已经存在了数十亿年,可能是原始生命中最早发现的一些酶。随着生命在这段漫长时间里不断进化,这些酶可能承担了与最初来源不同的新功能角色。在此,对这些酶进化史的研究既为SOD在生理学和疾病中的现代作用提供了解释,也引发了进一步的探究。