RNA granules and cytoskeletal links

被引:16
作者
Rajgor, Dipen [1 ,2 ]
Shanahan, Catherine M. [2 ]
机构
[1] Univ Cambridge, Dept Biochem, Cambridge CB2 1QW, England
[2] Kings Coll London, James Black Ctr, Div Cardiovasc, London WC2R 2LS, England
基金
英国医学研究理事会;
关键词
cytoskeleton; P-body; RNA granule; stress granule; STRESS GRANULES; PROCESSING BODIES; MESSENGER-RNAS; BODY FORMATION; GW BODIES; P-BODIES; TRANSLATION; TRANSPORT; MOVEMENT; SITES;
D O I
10.1042/BST20140067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In eukaryotic cells, non-translating mRNAs can accumulate into cytoplasmic mRNP (messenger ribonucleoprotein) granules such as P-bodies (processing bodies) and SGs (stress granules). P-bodies contain the mRNA decay and translational repression machineries and are ubiquitously expressed in mammalian cells and lower eukaryote species including Saccharomyces cerevisiae, Drosophila melanogaster and Caenorhabditis elegans. In contrast, SGs are only detected during cellular stress when translation is inhibited and form from aggregates of stalled pre-initiation complexes. SGs and P-bodies are related to NGs (neuronal granules), which are essential in the localization and control of mRNAs in neurons. Importantly, RNA granules are linked to the cytoskeleton, which plays an important role in mediating many of their dynamic properties. In the present review, we discuss how P-bodies, SGs and NGs are linked to cytoskeletal networks and the importance of these linkages in maintaining localization of their RNA cargoes.
引用
收藏
页码:1206 / 1210
页数:5
相关论文
共 38 条
[1]   The Dynamics of Mammalian P Body Transport, Assembly, and Disassembly In Vivo [J].
Aizer, Adva ;
Brody, Yehuda ;
Ler, Lian Wee ;
Sonenberg, Nahum ;
Singer, Robert H. ;
Shav-Tal, Yaron .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (10) :4154-4166
[2]   Stress granules [J].
Anderson, Paul ;
Kedersha, Nancy .
CURRENT BIOLOGY, 2009, 19 (10) :R397-R398
[3]   RNA granules: post-transcriptional and epigenetic modulators of gene expression [J].
Anderson, Paul ;
Kedersha, Nancy .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (06) :430-436
[4]   Stress-induced reversal of microRNA repression and mRNA P-body localization in human cells [J].
Bhattacharyya, S. N. ;
Habermacher, R. ;
Martine, U. ;
Closs, E. I. ;
Filipowicz, W. .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2006, 71 :513-521
[5]   Relief of microRNA-mediated translational repression in human cells subjected to stress [J].
Bhattacharyya, Suvendra N. ;
Habermacher, Regula ;
Martine, Ursula ;
Closs, Ellen I. ;
Filipowicz, Witold .
CELL, 2006, 125 (06) :1111-1124
[6]   Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies [J].
Brengues, M ;
Teixeira, D ;
Parker, R .
SCIENCE, 2005, 310 (5747) :486-489
[7]   Cytoplasmic foci are sites of mRNA decay in human cells [J].
Cougot, N ;
Babajko, S ;
Séraphin, B .
JOURNAL OF CELL BIOLOGY, 2004, 165 (01) :31-40
[8]   Cytoplasmic intermediate filaments revealed as dynamic and multipurpose scaffolds [J].
Coulombe, PA ;
Wong, P .
NATURE CELL BIOLOGY, 2004, 6 (08) :699-706
[9]   Hydrogen peroxide induces stress granule formation independent of eIF2α phosphorylation [J].
Emara, Mohamed M. ;
Fujimura, Ken ;
Sciaranghella, Daniele ;
Ivanova, Victoria ;
Ivanov, Pavel ;
Anderson, Paul .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 423 (04) :763-769
[10]   P-body formation is a consequence, not the cause, of RNA-mediated gene silencing [J].
Eulalio, Ana ;
Behm-Ansmant, Isabelle ;
Schweizer, Daniel ;
Izaurralde, Elisa .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (11) :3970-3981