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UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins

It is thought that the SelenoCysteine Insertion Sequence (SECIS) element and UGA codon are sufficient for selenocysteine (Sec) insertion. However, we found that UGA supported Sec insertion only at its natural position or in its close proximity in mammalian thioredoxin reductase 1 (TR1). In contrast,...

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Autores principales: Turanov, Anton A., Lobanov, Alexei V., Hatfield, Dolph L., Gladyshev, Vadim N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737529/
https://www.ncbi.nlm.nih.gov/pubmed/23716634
http://dx.doi.org/10.1093/nar/gkt409
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author Turanov, Anton A.
Lobanov, Alexei V.
Hatfield, Dolph L.
Gladyshev, Vadim N.
author_facet Turanov, Anton A.
Lobanov, Alexei V.
Hatfield, Dolph L.
Gladyshev, Vadim N.
author_sort Turanov, Anton A.
collection PubMed
description It is thought that the SelenoCysteine Insertion Sequence (SECIS) element and UGA codon are sufficient for selenocysteine (Sec) insertion. However, we found that UGA supported Sec insertion only at its natural position or in its close proximity in mammalian thioredoxin reductase 1 (TR1). In contrast, Sec could be inserted at any tested position in mammalian TR3. Replacement of the 3′-UTR of TR3 with the corresponding segment of a Euplotes crassus TR restricted Sec insertion into the C-terminal region, whereas the 3′-UTR of TR3 conferred unrestricted Sec insertion into E. crassus TR, in which Sec insertion is normally limited to the C-terminal region. Exchanges of 3′-UTRs between mammalian TR1 and E. crassus TR had no effect, as both proteins restricted Sec insertion. We further found that these effects could be explained by the use of selenoprotein-specific SECIS elements. Examination of Sec insertion into other selenoproteins was consistent with this model. The data indicate that mammals evolved the ability to limit Sec insertion into natural positions within selenoproteins, but do so in a selenoprotein-specific manner, and that this process is controlled by the SECIS element in the 3′-UTR.
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spelling pubmed-37375292013-08-08 UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins Turanov, Anton A. Lobanov, Alexei V. Hatfield, Dolph L. Gladyshev, Vadim N. Nucleic Acids Res Molecular Biology It is thought that the SelenoCysteine Insertion Sequence (SECIS) element and UGA codon are sufficient for selenocysteine (Sec) insertion. However, we found that UGA supported Sec insertion only at its natural position or in its close proximity in mammalian thioredoxin reductase 1 (TR1). In contrast, Sec could be inserted at any tested position in mammalian TR3. Replacement of the 3′-UTR of TR3 with the corresponding segment of a Euplotes crassus TR restricted Sec insertion into the C-terminal region, whereas the 3′-UTR of TR3 conferred unrestricted Sec insertion into E. crassus TR, in which Sec insertion is normally limited to the C-terminal region. Exchanges of 3′-UTRs between mammalian TR1 and E. crassus TR had no effect, as both proteins restricted Sec insertion. We further found that these effects could be explained by the use of selenoprotein-specific SECIS elements. Examination of Sec insertion into other selenoproteins was consistent with this model. The data indicate that mammals evolved the ability to limit Sec insertion into natural positions within selenoproteins, but do so in a selenoprotein-specific manner, and that this process is controlled by the SECIS element in the 3′-UTR. Oxford University Press 2013-08 2013-05-28 /pmc/articles/PMC3737529/ /pubmed/23716634 http://dx.doi.org/10.1093/nar/gkt409 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Turanov, Anton A.
Lobanov, Alexei V.
Hatfield, Dolph L.
Gladyshev, Vadim N.
UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
title UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
title_full UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
title_fullStr UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
title_full_unstemmed UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
title_short UGA codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
title_sort uga codon position-dependent incorporation of selenocysteine into mammalian selenoproteins
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737529/
https://www.ncbi.nlm.nih.gov/pubmed/23716634
http://dx.doi.org/10.1093/nar/gkt409
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