Literature DB >> 16520386

RNA granules.

Paul Anderson1, Nancy Kedersha.   

Abstract

Cytoplasmic RNA granules in germ cells (polar and germinal granules), somatic cells (stress granules and processing bodies), and neurons (neuronal granules) have emerged as important players in the posttranscriptional regulation of gene expression. RNA granules contain various ribosomal subunits, translation factors, decay enzymes, helicases, scaffold proteins, and RNA-binding proteins, and they control the localization, stability, and translation of their RNA cargo. We review the relationship between different classes of these granules and discuss how spatial organization regulates messenger RNA translation/decay.

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Year:  2006        PMID: 16520386      PMCID: PMC2063724          DOI: 10.1083/jcb.200512082

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  60 in total

1.  DcpS can act in the 5'-3' mRNA decay pathway in addition to the 3'-5' pathway.

Authors:  Erwin van Dijk; Hervé Le Hir; Bertrand Séraphin
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-01       Impact factor: 11.205

2.  Decapping and decay of messenger RNA occur in cytoplasmic processing bodies.

Authors:  Ujwal Sheth; Roy Parker
Journal:  Science       Date:  2003-05-02       Impact factor: 47.728

Review 3.  Transcriptional silencing and translational control: key features of early germline development.

Authors:  Judith L Leatherman; Thomas A Jongens
Journal:  Bioessays       Date:  2003-04       Impact factor: 4.345

4.  Human Dcp2: a catalytically active mRNA decapping enzyme located in specific cytoplasmic structures.

Authors:  Erwin van Dijk; Nicolas Cougot; Sylke Meyer; Sylvie Babajko; Elmar Wahle; Bertrand Séraphin
Journal:  EMBO J       Date:  2002-12-16       Impact factor: 11.598

5.  Mammalian stress granules represent sites of accumulation of stalled translation initiation complexes.

Authors:  Scot R Kimball; Rick L Horetsky; David Ron; Leonard S Jefferson; Heather P Harding
Journal:  Am J Physiol Cell Physiol       Date:  2002-10-03       Impact factor: 4.249

6.  MK2-induced tristetraprolin:14-3-3 complexes prevent stress granule association and ARE-mRNA decay.

Authors:  Georg Stoecklin; Tiffany Stubbs; Nancy Kedersha; Stephen Wax; William F C Rigby; T Keith Blackwell; Paul Anderson
Journal:  EMBO J       Date:  2004-03-11       Impact factor: 11.598

7.  The GW182 protein colocalizes with mRNA degradation associated proteins hDcp1 and hLSm4 in cytoplasmic GW bodies.

Authors:  Theophany Eystathioy; Andrew Jakymiw; Edward K L Chan; Bertrand Séraphin; Nicolas Cougot; Marvin J Fritzler
Journal:  RNA       Date:  2003-10       Impact factor: 4.942

8.  BDNF induces translocation of initiation factor 4E to mRNA granules: evidence for a role of synaptic microfilaments and integrins.

Authors:  Fiona M Smart; Gerald M Edelman; Peter W Vanderklish
Journal:  Proc Natl Acad Sci U S A       Date:  2003-11-17       Impact factor: 11.205

9.  Stressful initiations.

Authors:  Paul Anderson; Nancy Kedersha
Journal:  J Cell Sci       Date:  2002-08-15       Impact factor: 5.285

10.  The RasGAP-associated endoribonuclease G3BP assembles stress granules.

Authors:  Helene Tourrière; Karim Chebli; Latifa Zekri; Brice Courselaud; Jean Marie Blanchard; Edouard Bertrand; Jamal Tazi
Journal:  J Cell Biol       Date:  2003-03-17       Impact factor: 10.539

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  469 in total

1.  The stress granule protein G3BP1 binds viral dsRNA and RIG-I to enhance interferon-β response.

Authors:  Susana Soo-Yeon Kim; Lynette Sze; ChengCheng Liu; Kong-Peng Lam
Journal:  J Biol Chem       Date:  2019-02-25       Impact factor: 5.157

2.  A genome-wide RNAi screen identifies genes regulating the formation of P bodies in C. elegans and their functions in NMD and RNAi.

Authors:  Yinyan Sun; Peiguo Yang; Yuxia Zhang; Xin Bao; Jun Li; Wenru Hou; Xiangyu Yao; Jinghua Han; Hong Zhang
Journal:  Protein Cell       Date:  2011-12-17       Impact factor: 14.870

3.  3'-UTR-located inverted Alu repeats facilitate mRNA translational repression and stress granule accumulation.

Authors:  Terry Fitzpatrick; Sui Huang
Journal:  Nucleus       Date:  2012-06-12       Impact factor: 4.197

Review 4.  P-bodies and stress granules: possible roles in the control of translation and mRNA degradation.

Authors:  Carolyn J Decker; Roy Parker
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-09-01       Impact factor: 10.005

5.  Evidence for translational regulation by the herpes simplex virus virion host shutoff protein.

Authors:  Holly A Saffran; G Sullivan Read; James R Smiley
Journal:  J Virol       Date:  2010-03-31       Impact factor: 5.103

6.  Dynein motor contributes to stress granule dynamics in primary neurons.

Authors:  N-P Tsai; Y-C Tsui; L-N Wei
Journal:  Neuroscience       Date:  2009-01-03       Impact factor: 3.590

7.  Oxidative Stress Increases the Number of Stress Granules in Senescent Cells and Triggers a Rapid Decrease in p21waf1/cip1 Translation.

Authors:  Xian Jin Lian; Imed-Eddine Gallouzi
Journal:  J Biol Chem       Date:  2009-01-28       Impact factor: 5.157

Review 8.  mRNA localization: gene expression in the spatial dimension.

Authors:  Kelsey C Martin; Anne Ephrussi
Journal:  Cell       Date:  2009-02-20       Impact factor: 41.582

9.  Microtubule-dependent association of AKAP350A and CCAR1 with RNA stress granules.

Authors:  Elena Kolobova; Andrey Efimov; Irina Kaverina; Arun K Rishi; John W Schrader; Amy-Joan Ham; M Cecilia Larocca; James R Goldenring
Journal:  Exp Cell Res       Date:  2008-12-03       Impact factor: 3.905

10.  Processing-body movement in Arabidopsis depends on an interaction between myosins and DECAPPING PROTEIN1.

Authors:  Alexandra Steffens; Benjamin Jaegle; Achim Tresch; Martin Hülskamp; Marc Jakoby
Journal:  Plant Physiol       Date:  2014-02-13       Impact factor: 8.340

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