SKAR links pre-mRNA splicing to mTOR/S6K1-mediated enhanced translation efficiency of spliced mRNAs (Q24323236)

DNA polymerase delta interacting protein 3

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Eukaryotic translation initiation factor 4A3

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positive regulation of translation

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5

John Blenis

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author name string

Xiaoju Max Ma

1

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Sang-Oh Yoon

2

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Celeste J Richardson

3

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Kristina Jülich

A nuclear cap binding protein complex involved in pre-mRNA splicing

4

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language of work or name

English

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publication date

18 April 2008

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language of work

Cell

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volume

133

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issue

2

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page(s)

303-13

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cites work

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The ever-increasing complexities of the exon junction complex

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Mechanistic links between nonsense-mediated mRNA decay and pre-mRNA splicing in mammalian cells

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TREX, SR proteins and export of mRNA.

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mTOR and S6K1 mediate assembly of the translation preinitiation complex through dynamic protein interchange and ordered phosphorylation events

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Human mRNA export machinery recruited to the 5' end of mRNA

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SKAR is a specific target of S6 kinase 1 in cell growth control

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A new function for nonsense-mediated mRNA-decay factors

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Evidence for a pioneer round of mRNA translation: mRNAs subject to nonsense-mediated decay in mammalian cells are bound by CBP80 and CBP20

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Translation is required to remove Y14 from mRNAs in the cytoplasm

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How introns influence and enhance eukaryotic gene expression

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Pre-mRNA splicing imprints mRNA in the nucleus with a novel RNA-binding protein that persists in the cytoplasm

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Purification and characterization of native spliceosomes suitable for three-dimensional structural analysis

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Shuttling of pre-mRNA binding proteins between nucleus and cytoplasm

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Comprehensive proteomic analysis of the human spliceosome

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eIF4AIII binds spliced mRNA in the exon junction complex and is essential for nonsense-mediated decay

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eIF4G is required for the pioneer round of translation in mammalian cells

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RNA splicing promotes translation and RNA surveillance

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Target of rapamycin (TOR): an integrator of nutrient and growth factor signals and coordinator of cell growth and cell cycle progression

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Exon junction complexes mediate the enhancing effect of splicing on mRNA expression

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Heterologous introns can enhance expression of transgenes in mice

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A simple whole cell lysate system for in vitro splicing reveals a stepwise assembly of the exon-exon junction complex

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Nuclear history of a pre-mRNA determines the translational activity of cytoplasmic mRNA.

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The spliceosome deposits multiple proteins 20-24 nucleotides upstream of mRNA exon-exon junctions

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Magoh, a human homolog of Drosophila mago nashi protein, is a component of the splicing-dependent exon-exon junction complex

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The role of Upf proteins in modulating the translation read-through of nonsense-containing transcripts

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The exon junction complex is detected on CBP80-bound but not eIF4E-bound mRNA in mammalian cells: dynamics of mRNP remodeling

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Pseudouridylation (Psi) of U2 snRNA in S. cerevisiae is catalyzed by an RNA-independent mechanism

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Intron-less RNA injected into the nucleus of Xenopus oocytes accesses a regulated translation control pathway

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Introns increase gene expression in cultured maize cells

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Splicing enhances translation in mammalian cells: an additional function of the exon junction complex

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The pioneer translation initiation complex is functionally distinct from but structurally overlaps with the steady-state translation initiation complex

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Upstream and downstream of mTOR

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Regulation of translation initiation by FRAP/mTOR

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S6K1- and betaTRCP-mediated degradation of PDCD4 promotes protein translation and cell growth

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eIF4 initiation factors: effectors of mRNA recruitment to ribosomes and regulators of translation

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The nonsense-mediated decay RNA surveillance pathway

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A quantitative analysis of intron effects on mammalian gene expression

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Analysis of the stimulatory effect of splicing on mRNA production and utilization in mammalian cells

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