Nonsense-mediated decay: assaying for effects on selenoprotein mRNAs (Q43920331)

28 November 2017

title

Nonsense-mediated decay: assaying for effects on selenoprotein mRNAs (English)

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28 November 2017

2

Lynne E Maquat

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28 November 2017

Xiaolei Sun

1

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28 November 2017

language of work or name

English

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publication date

1 January 2002

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28 November 2017

published in

Methods in Enzymology

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28 November 2017

volume

347

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28 November 2017

page(s)

49-57

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

28 November 2017

cites work

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The selenium requirement for glutathione peroxidase mRNA level is half of the selenium requirement for glutathione peroxidase activity in female rats

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Selenium deficiency reduces the abundance of mRNA for Se-dependent glutathione peroxidase 1 by a UGA-dependent mechanism likely to be nonsense codon-mediated decay of cytoplasmic mRNA.

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Selective control of cytosolic glutathione peroxidase and phospholipid hydroperoxide glutathione peroxidase mRNA stability by selenium supply

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

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Analysis of eukaryotic mRNA structures directing cotranslational incorporation of selenocysteine

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Nonsense Surveillance in Lymphocytes?

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A perfect message: RNA surveillance and nonsense-mediated decay

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Intron function in the nonsense-mediated decay of beta-globin mRNA: indications that pre-mRNA splicing in the nucleus can influence mRNA translation in the cytoplasm

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At least one intron is required for the nonsense-mediated decay of triosephosphate isomerase mRNA: a possible link between nuclear splicing and cytoplasmic translation

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A rule for termination-codon position within intron-containing genes: when nonsense affects RNA abundance

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

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A mutated human homologue to yeast Upf1 protein has a dominant-negative effect on the decay of nonsense-containing mRNAs in mammalian cells

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Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA.

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Identifiers

DOI

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28 November 2017

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