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Human SepSecS or SLA/LP: selenocysteine formation and autoimmune hepatitis

期刊

BIOLOGICAL CHEMISTRY
卷 391, 期 7, 页码 771-776

出版社

WALTER DE GRUYTER GMBH
DOI: 10.1515/BC.2010.078

关键词

selenium; selenocysteine tRNA; Sep-tRNA:Sec-tRNA synthase; Soluble Liver Antigen/Liver Pancreas; stop codon recoding; UGA recoding

资金

  1. Department of Energy
  2. National Institute for General Medical Sciences
  3. National Science Foundation
  4. Yale University School of Medicine

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Selenocysteine, the 21st genetically encoded amino acid, is the major form of the antioxidant trace element selenium in the human body. In eukaryotes and archaea its synthesis proceeds through a phosphorylated intermediate in a tRNA-dependent fashion. The final step of selenocysteine formation is catalyzed by O-phosphoseryl-tRNA:selenocysteinyl-tRNA synthase (SepSecS) that converts phosphoseryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec). The human SepSecS protein is also known as soluble liver antigen/liver pancreas (SLA/LP), which represents one of the antigens of autoimmune hepatitis. Here we review the discovery of human SepSecS and the current understanding of the immunogenicity of SLA/LP in autoimmune hepatitis.

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