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硒蛋白和硒代半胱氨酸生物合成机制中的致病变体。

Pathogenic Variants in Selenoproteins and Selenocysteine Biosynthesis Machinery.

机构信息

Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Int J Mol Sci. 2021 Oct 27;22(21):11593. doi: 10.3390/ijms222111593.

Abstract

Selenium is incorporated into selenoproteins as the 21st amino acid selenocysteine (Sec). There are 25 selenoproteins encoded in the human genome, and their synthesis requires a dedicated machinery. Most selenoproteins are oxidoreductases with important functions in human health. A number of disorders have been associated with deficiency of selenoproteins, caused by mutations in selenoprotein genes or Sec machinery genes. We discuss mutations that are known to cause disease in humans and report their allele frequencies in the general population. The occurrence of protein-truncating variants in the same genes is also presented. We provide an overview of pathogenic variants in selenoproteins genes from a population genomics perspective.

摘要

硒作为第 21 种氨基酸——硒代半胱氨酸(Sec)被掺入到硒蛋白中。人类基因组中编码了 25 种硒蛋白,其合成需要专门的机制。大多数硒蛋白是氧化还原酶,在人类健康中具有重要功能。一些疾病与硒蛋白缺乏有关,这是由于硒蛋白基因或 Sec 机制基因发生突变引起的。我们讨论了已知会导致人类疾病的突变,并报告了它们在普通人群中的等位基因频率。还呈现了相同基因中导致蛋白截断的变异体的发生情况。我们从群体基因组学的角度概述了硒蛋白基因中的致病变异体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/8584023/e1d2afaa32aa/ijms-22-11593-g001.jpg

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