Re-programming of translation following cell stress allows IRES-mediated translation to predominate. - Wikidata - wikimedia - TriplyDB

Re-programming of translation following cell stress allows IRES-mediated translation to predominate.

Re-programming of translation following cell stress allows IRES-mediated translation to predominate.

http://www.wikidata.org/entity/Q37029410

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Diverse RNA-binding proteins interact with functionally related sets of RNAs, suggesting an extensive regulatory system Translational control in the stress adaptive response of cancer cells: a novel role for the heat shock protein TRAP1 Regulation of mRNA cap methylation Translational Control of the HIV Unspliced Genomic RNA Localized IRES-dependent translation of ER chaperone protein mRNA in sensory axons RPS25 is essential for translation initiation by the Dicistroviridae and hepatitis C viral IRESs Diverse diseases from a ubiquitous process: the ribosomopathy paradox The Sua5 protein is essential for normal translational regulation in yeast.Rpl22 is required for IME1 mRNA translation and meiotic induction in S. cerevisiae.Translation initiation: variations in the mechanism can be anticipated Inflammatory conditions induce IRES-dependent translation of cyp24a1 Elaborate uORF/IRES features control expression and localization of human glycyl-tRNA synthetase Differential regulation of polysome mRNA levels in mouse Hepa-1C1C7 cells exposed to dioxin Eukaryotic stress granules: the ins and outs of translation eEF2 and Ras-GAP SH3 domain-binding protein (G3BP1) modulate stress granule assembly during HIV-1 infection Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6 FGF2 translationally induced by hypoxia is involved in negative and positive feedback loops with HIF-1alpha.Translational reprogramming following UVB irradiation is mediated by DNA-PKcs and allows selective recruitment to the polysomes of mRNAs encoding DNA repair enzymes.N-terminal proteomics and ribosome profiling provide a comprehensive view of the alternative translation initiation landscape in mice and men Involvement of 4E-BP1 in the protection induced by HDLs on pancreatic beta-cells.Initiation factor eIF2-independent mode of c-Src mRNA translation occurs via an internal ribosome entry site.Specialized ribosomes: a new frontier in gene regulation and organismal biology.Transcriptional control of human antigen R by bone morphogenetic protein LIN-35/Rb causes starvation-induced germ cell apoptosis via CED-9/Bcl2 downregulation in Caenorhabditis elegans.A highly conserved family of domains related to the DNA-glycosylase fold helps predict multiple novel pathways for RNA modifications Internal ribosome entry site of bFGF is the target of thalidomide for IMiDs development in multiple myeloma.The multifunctional SNM1 gene family: not just nucleases Toward a structural understanding of IRES RNA function Stress-inducible alternative translation initiation of human cytomegalovirus latency protein pUL138.BH3-only protein Bmf mediates apoptosis upon inhibition of CAP-dependent protein synthesis.The human IGF1R IRES likely operates through a Shine-Dalgarno-like interaction with the G961 loop (E-site) of the 18S rRNA and is kinetically modulated by a naturally polymorphic polyU loop.EIF2A-dependent translational arrest protects leukemia cells from the energetic stress induced by NAMPT inhibition Comprehensive structural annotation of Pichia pastoris transcriptome and the response to various carbon sources using deep paired-end RNA sequencing.Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning Cellular IRES-mediated translation: the war of ITAFs in pathophysiological states.PI3K-mTORC1 attenuates stress response by inhibiting cap-independent Hsp70 translation.The genetic code as expressed through relationships between mRNA structure and protein function.Genome-wide profiling of human cap-independent translation-enhancing elements.BRCA1-Dependent Translational Regulation in Breast Cancer Cells.Phosphomimetic substitution of heterogeneous nuclear ribonucleoprotein A1 at serine 199 abolishes AKT-dependent internal ribosome entry site-transacting factor (ITAF) function via effects on strand annealing and results in mammalian target of rapamy

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Re-programming of translation following cell stress allows IRES-mediated translation to predominate.

http://www.wikidata.org/entity/Q37029410

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on January 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Re-programming of translation ...... ed translation to predominate.

@en

Re-programming of translation ...... ed translation to predominate.

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type

label

Re-programming of translation ...... ed translation to predominate.

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Re-programming of translation ...... ed translation to predominate.

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prefLabel

Re-programming of translation ...... ed translation to predominate.

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Re-programming of translation ...... ed translation to predominate.

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Biology of the Cell

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Re-programming of translation ...... ed translation to predominate.

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Anne E Willis

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Keith A Spriggs

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Mark Stoneley

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Martin Bushell

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P2860

Identification and characterization of a novel cell cycle-regulated internal ribosome entry site

4E-BP3, a new member of the eukaryotic initiation factor 4E-binding protein family

Insulin-dependent stimulation of protein synthesis by phosphorylation of a regulator of 5'-cap function

Hypoxia-inducible factor-1alpha mRNA contains an internal ribosome entry site that allows efficient translation during normoxia and hypoxia

UNR translation can be driven by an IRES element that is negatively regulated by polypyrimidine tract binding protein

Regulation of protein synthesis by hypoxia via activation of the endoplasmic reticulum kinase PERK and phosphorylation of the translation initiation factor eIF2alpha.

Hypoxia inhibits protein synthesis through a 4E-BP1 and elongation factor 2 kinase pathway controlled by mTOR and uncoupled in breast cancer cells

Suppression of cap-dependent translation in mitosis

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

The Apaf-1 internal ribosome entry segment attains the correct structural conformation for function via interactions with PTB and unr

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27-38

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scholarly article

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10.1042/BC20070098

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1

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100

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2008-01-01T00:00:00Z

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18072942

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