Nuclear assembly of UGA decoding complexes on selenoprotein mRNAs: a mechanism for eluding nonsense-mediated decay? - Wikidata - wikimedia - TriplyDB

Nuclear assembly of UGA decoding complexes on selenoprotein mRNAs: a mechanism for eluding nonsense-mediated decay?

Nuclear assembly of UGA decoding complexes on selenoprotein mRNAs: a mechanism for eluding nonsense-mediated decay?

http://www.wikidata.org/entity/Q40316297

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An improved definition of the RNA-binding specificity of SECIS-binding protein 2, an essential component of the selenocysteine incorporation machinery The human selenoproteome: recent insights into functions and regulation Cellular and molecular basis of deiodinase-regulated thyroid hormone signaling Does constructive neutral evolution play an important role in the origin of cellular complexity? Making sense of the origins and uses of biological complexity Supramolecular complexes mediate selenocysteine incorporation in vivo Selective up-regulation of human selenoproteins in response to oxidative stress Threading the needle: getting selenocysteine into proteins Hypermethylated-capped selenoprotein mRNAs in mammals.Regulation and function of selenoproteins in human disease Impact of trivalent arsenicals on selenoprotein synthesis The selenoproteome exhibits widely varying, tissue-specific dependence on selenoprotein P for selenium supply.The Selenocysteine-Specific Elongation Factor Contains Unique Sequences That Are Required for Both Nuclear Export and Selenocysteine Incorporation.Arsenic trioxide and auranofin inhibit selenoprotein synthesis: implications for chemotherapy for acute promyelocytic leukaemia.Functional characterization of alternatively spliced human SECISBP2 transcript variants.Exposure to monomethylarsonous acid (MMA(III)) leads to altered selenoprotein synthesis in a primary human lung cell model.Interplay between selenium levels, selenoprotein expression, and replicative senescence in WI-38 human fibroblasts.Characterization of the UGA-recoding and SECIS-binding activities of SECIS-binding protein 2 SBP2 binding affinity is a major determinant in differential selenoprotein mRNA translation and sensitivity to nonsense-mediated decay.

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Nuclear assembly of UGA decoding complexes on selenoprotein mRNAs: a mechanism for eluding nonsense-mediated decay?

http://www.wikidata.org/entity/Q40316297

description

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Nuclear assembly of UGA decodi ...... uding nonsense-mediated decay?

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MCB.26.5.1795-1805.2006

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Molecular and Cellular Biology

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Nuclear assembly of UGA decodi ...... uding nonsense-mediated decay?

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Andrea Small-Howard

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Erin P Forry

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John W Harney

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Lucia A de Jesus

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Marla J Berry

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Nadya Morozova

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Peter R Hoffmann

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Robert J Stillwell

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Tanya Michaud

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P2860

A novel shuttling protein, 4E-T, mediates the nuclear import of the mRNA 5' cap-binding protein, eIF4E

Human Upf proteins target an mRNA for nonsense-mediated decay when bound downstream of a termination codon

Functional characterization of the eukaryotic SECIS elements which direct selenocysteine insertion at UGA codons

Tight control of gene expression in mammalian cells by tetracycline-responsive promoters

A novel RNA binding protein, SBP2, is required for the translation of mammalian selenoprotein mRNAs

Nonsense-mediated mRNA decay in Drosophila: at the intersection of the yeast and mammalian pathways

Selenium regulation of transcript abundance and translational efficiency of glutathione peroxidase-1 and -4 in rat liver

Nonsense-mediated decay of mRNA for the selenoprotein phospholipid hydroperoxide glutathione peroxidase is detectable in cultured cells but masked or inhibited in rat tissues

Decoding apparatus for eukaryotic selenocysteine insertion.

Ribosomal protein L30 is a component of the UGA-selenocysteine recoding machinery in eukaryotes

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1795-1805

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10.1128/MCB.26.5.1795-1805.2006

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