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本文引用的文献

1
Contribution of selenocysteine to the peroxidase activity of selenoprotein S.硒代半胱氨酸对硒蛋白 S 过氧化物酶活性的贡献。
Biochemistry. 2013 Aug 20;52(33):5514-6. doi: 10.1021/bi400741c. Epub 2013 Aug 12.
2
The PACAP-regulated gene selenoprotein T is abundantly expressed in mouse and human β-cells and its targeted inactivation impairs glucose tolerance.PACAP 调节的基因硒蛋白 T 在小鼠和人β细胞中大量表达,其靶向失活会损害葡萄糖耐量。
Endocrinology. 2013 Oct;154(10):3796-806. doi: 10.1210/en.2013-1167. Epub 2013 Aug 2.
3
MsrB1 and MICALs regulate actin assembly and macrophage function via reversible stereoselective methionine oxidation.MsrB1 和 MICALs 通过可逆立体选择性蛋氨酸氧化调节肌动蛋白组装和巨噬细胞功能。
Mol Cell. 2013 Aug 8;51(3):397-404. doi: 10.1016/j.molcel.2013.06.019. Epub 2013 Aug 1.
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Selective activation of oxidized PTP1B by the thioredoxin system modulates PDGF-β receptor tyrosine kinase signaling.硫氧还蛋白系统选择性激活氧化型 PTP1B 调节 PDGF-β 受体酪氨酸激酶信号转导。
Proc Natl Acad Sci U S A. 2013 Aug 13;110(33):13398-403. doi: 10.1073/pnas.1302891110. Epub 2013 Jul 30.
5
Deletion of selenoprotein M leads to obesity without cognitive deficits.硒蛋白 M 缺失导致肥胖而认知功能无缺陷。
J Biol Chem. 2013 Sep 6;288(36):26121-26134. doi: 10.1074/jbc.M113.471235. Epub 2013 Jul 23.
6
Selenium and diabetes--evidence from animal studies.硒与糖尿病——来自动物研究的证据。
Free Radic Biol Med. 2013 Dec;65:1548-1556. doi: 10.1016/j.freeradbiomed.2013.07.012. Epub 2013 Jul 16.
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Selenocysteine confers resistance to inactivation by oxidation in thioredoxin reductase: comparison of selenium and sulfur enzymes.硒半胱氨酸赋予硫氧还蛋白还原酶抗氧化失活的抗性:硒酶和硫酶的比较。
Biochemistry. 2013 Aug 13;52(32):5472-81. doi: 10.1021/bi400462j. Epub 2013 Jul 31.
8
SECISearch3 and Seblastian: new tools for prediction of SECIS elements and selenoproteins.SECISearch3 和 Seblastian:预测 SECIS 元件和硒蛋白的新工具。
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A Txnrd1-dependent metabolic switch alters hepatic lipogenesis, glycogen storage, and detoxification.Txnrd1 依赖性代谢转换改变肝脏的脂肪生成、糖原储存和解毒功能。
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10
UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins.UGA 密码子位置依赖性地将硒代半胱氨酸掺入哺乳动物硒蛋白中。
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硒蛋白:分子途径与生理作用

Selenoproteins: molecular pathways and physiological roles.

作者信息

Labunskyy Vyacheslav M, Hatfield Dolph L, Gladyshev Vadim N

机构信息

Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts; and Molecular Biology of Selenium Section, Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

出版信息

Physiol Rev. 2014 Jul;94(3):739-77. doi: 10.1152/physrev.00039.2013.

DOI:10.1152/physrev.00039.2013
PMID:24987004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4101630/
Abstract

Selenium is an essential micronutrient with important functions in human health and relevance to several pathophysiological conditions. The biological effects of selenium are largely mediated by selenium-containing proteins (selenoproteins) that are present in all three domains of life. Although selenoproteins represent diverse molecular pathways and biological functions, all these proteins contain at least one selenocysteine (Sec), a selenium-containing amino acid, and most serve oxidoreductase functions. Sec is cotranslationally inserted into nascent polypeptide chains in response to the UGA codon, whose normal function is to terminate translation. To decode UGA as Sec, organisms evolved the Sec insertion machinery that allows incorporation of this amino acid at specific UGA codons in a process requiring a cis-acting Sec insertion sequence (SECIS) element. Although the basic mechanisms of Sec synthesis and insertion into proteins in both prokaryotes and eukaryotes have been studied in great detail, the identity and functions of many selenoproteins remain largely unknown. In the last decade, there has been significant progress in characterizing selenoproteins and selenoproteomes and understanding their physiological functions. We discuss current knowledge about how these unique proteins perform their functions at the molecular level and highlight new insights into the roles that selenoproteins play in human health.

摘要

硒是一种必需的微量营养素,在人类健康中具有重要功能,并与多种病理生理状况相关。硒的生物学效应很大程度上由含硒蛋白(硒蛋白)介导,这些蛋白存在于生命的所有三个域中。尽管硒蛋白代表了不同的分子途径和生物学功能,但所有这些蛋白都至少含有一个硒代半胱氨酸(Sec),一种含硒氨基酸,并且大多数发挥氧化还原酶功能。Sec在共翻译过程中响应UGA密码子插入新生多肽链,UGA的正常功能是终止翻译。为了将UGA解码为Sec,生物体进化出了Sec插入机制,该机制允许在需要顺式作用的Sec插入序列(SECIS)元件的过程中,在特定的UGA密码子处掺入这种氨基酸。尽管对原核生物和真核生物中Sec合成及插入蛋白质的基本机制已进行了详细研究,但许多硒蛋白的身份和功能仍 largely unknown。在过去十年中,在表征硒蛋白和硒蛋白组以及了解它们的生理功能方面取得了重大进展。我们讨论了关于这些独特蛋白如何在分子水平上发挥功能的当前知识,并强调了对硒蛋白在人类健康中所起作用的新见解。