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Identity and Function of Selenoprotein Genes


Biography

Overview
Selenium is an essential trace element that has roles in cancer prevention, the immune system, brain function, and male reproduction. This element is present in proteins in the form of selenocysteine residue, which is co-translationally inserted into proteins in response to UGA codons. Mutations or single nucleotide polymorphisms in several selenoprotein genes and selenocysteine machinery genes have been associated with disease. Selenocysteine insertion is dependent on the SECIS element, a stem-loop structure present in 3'-untranslated regions of selenoprotein genes. Because UGA codon normally functions as a stop signal, selenoprotein genes are often missed by genome annotation programs. We developed bioinformatics tools that allow identification of selenoprotein genes by searching for SECIS elements and selenocysteine/cysteine pairs in homologous sequences. Using these tools, we identified sets of human and mouse selenoproteins (selenoproteomes). We suggest that in order to understand biological and biomedical effects of dietary selenium, information on identifies and functions of all selenoproteins is required. We propose to address critical questions in the area of selenium biology and its role in human health, including dependence of selenocysteine insertion on the location of UGA codon within coding sequences of selenoprotein genes, comprehensive characterization of mammalian selenoproteomes through bioinformatics and imaging approaches, and analysis of biological functions of an emerging class of endoplasmic reticulum-resident selenoproteins. The three specific aims of this application are as follows: (1) Position-dependent insertion of selenocysteine into mammalian selenoproteins. (2) Characterization of mammalian selenoproteomes. (3) Roles of Selenoprotein S and Selenoprotein K in mammalian endoplasmic reticulum-associated protein degradation. A combination of cell biology, biochemistry, bioinformatics, imaging and animal model approaches will be used to address these questions.
R01GM061603
GLADYSHEV, VADIM N.

Time
2000-07-01
2017-06-30
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.