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Journal ArticleDOI

Stress granules: the Tao of RNA triage

Paul A. Anderson, +1 more
- 01 Mar 2008 - 
- Vol. 33, Iss: 3, pp 141-150
TLDR
Although both self-assemble in response to stress-induced perturbations in translation, several recent reports reveal novel proteins and RNAs that are components of these structures but also perform other cellular functions.
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This article is published in Trends in Biochemical Sciences.The article was published on 2008-03-01. It has received 1024 citations till now. The article focuses on the topics: Stress granule & P-bodies.

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Citations
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Journal ArticleDOI

Regulation of Translation Initiation in Eukaryotes: Mechanisms and Biological Targets

TL;DR: Recent advances in understanding of the molecular structures and biochemical functions of the translation initiation machinery are described and key strategies that mediate general or gene-specific translational control are summarized, particularly in mammalian systems.
Journal ArticleDOI

MicroRNA and cancer.

TL;DR: The current knowledge and concepts concerning the involvement of microRNAs in cancer, which have emerged from the study of cell culture and animal model systems, including the regulation of key cancer‐related pathways, such as cell cycle control and the DNA damage response are summarized.
Journal ArticleDOI

Protein arginine methyltransferases and cancer.

TL;DR: There are nine protein arginine methyltransferases (PRMTs) encoded in mammalian genomes, the protein products of which catalyse three types of ARG modifications: monomethylation and two types of dimethylation as discussed by the authors.
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RNA granules: post-transcriptional and epigenetic modulators of gene expression

TL;DR: It is proposed that RNA granules can be both a cause and a consequence of altered mRNA translation, decay or editing and serve as key modulators of post-transcriptional and epigenetic gene expression.
Journal ArticleDOI

MicroRNA functions in stress responses.

TL;DR: This work has shown that miRNAs play key roles in fundamental cellular processes, including how cells respond to changes in environment or stresses, and dysregulation of these processes contributes to chronic diseases, including cancers.
References
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Journal ArticleDOI

Regulated Translation Initiation Controls Stress-Induced Gene Expression in Mammalian Cells

TL;DR: Protein kinases that phosphorylate the alpha subunit of eukaryotic initiation factor 2 (eIF2alpha) are activated in stressed cells and negatively regulate protein synthesis, resulting in the induction of the downstream gene CHOP (GADD153).
Journal ArticleDOI

Perk Is Essential for Translational Regulation and Cell Survival during the Unfolded Protein Response

TL;DR: In this paper, the authors report that mutating the gene encoding the ER stress-activated eIF2alpha kinase PERK abolishes the phosphorylation of eIF 2 alpha in response to accumulation of malfolded proteins in the ER resulting in abnormally elevated protein synthesis and higher levels of ER stress.
Journal ArticleDOI

Stress granules and processing bodies are dynamically linked sites of mRNP remodeling

TL;DR: It is proposed that mRNA released from disassembled polysomes is sorted and remodeled at SGs, from which selected transcripts are delivered to PBs for degradation, an interaction that is promoted by the related mRNA decay factors TTP and BRF1.
Journal ArticleDOI

P Bodies and the Control of mRNA Translation and Degradation

TL;DR: An emerging model of cytoplasmic mRNA function is suggested in which the rates of translation and degradation of mRNAs are influenced by a dynamic equilibrium between polysomes and the mRNPs seen in P bodies.
Journal ArticleDOI

Decapping and Decay of Messenger RNA Occur in Cytoplasmic Processing Bodies

TL;DR: The flux of mRNAs between polysomes and P bodies is defined as a critical aspect of cytoplasmic mRNA metabolism and a possible site for regulation of mRNA degradation.
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