Altered Ribostasis: RNA-Protein Granules in Degenerative Disorders

被引:481
作者
Ramaswami, Mani [1 ,2 ,3 ]
Taylor, J. Paul [4 ]
Parker, Roy [5 ,6 ]
机构
[1] Trinity Coll Dublin, Sch Genet & Microbiol, Dublin 2, Ireland
[2] Trinity Coll Dublin, Sch Nat Sci, Smurfit Inst Genet, Dublin 2, Ireland
[3] Trinity Coll Dublin, Trinity Coll Inst Neurosci, Dublin 2, Ireland
[4] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38120 USA
[5] Univ Colorado, Dept Biochem & Chem, Boulder, CO 80309 USA
[6] Univ Colorado, Howard Hughes Med Inst, Boulder, CO 80309 USA
基金
爱尔兰科学基金会;
关键词
LENGTH POLYGLUTAMINE EXPANSIONS; EUKARYOTIC STRESS GRANULES; ALZHEIMERS-DISEASE; MESSENGER-RNA; HEXANUCLEOTIDE REPEAT; DROSOPHILA MODEL; NUCLEAR FOCI; P-BODIES; TDP-43; NEURODEGENERATION;
D O I
10.1016/j.cell.2013.07.038
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
The molecular processes that contribute to degenerative diseases are not well understood. Recent observations suggest that some degenerative diseases are promoted by the accumulation of nuclear or cytoplasmic RNA-protein (RNP) aggregates, which can be related to endogenous RNP granules. RNP aggregates arise commonly in degenerative diseases because RNA-binding proteins commonly self-assemble, in part through prion-like domains, which can form self-propagating amyloids. RNP aggregates may be toxic due to multiple perturbations of posttranscriptional control, thereby disrupting the normal "ribostasis" of the cell. This suggests that understanding and modulating RNP assembly or clearance may be effective approaches to developing therapies for these diseases.
引用
收藏
页码:727 / 736
页数:10
相关论文
共 101 条
[1]   The Transcellular Spread of Cytosolic Amyloids, Prions, and Prionoids [J].
Aguzzi, Adriano ;
Rajendran, Lawrence .
NEURON, 2009, 64 (06) :783-790
[2]   Stress granules [J].
Anderson, Paul ;
Kedersha, Nancy .
CURRENT BIOLOGY, 2009, 19 (10) :R397-R398
[3]  
[Anonymous], P NATL ACAD SCI US
[4]   Adapting proteostasis for disease intervention [J].
Balch, William E. ;
Morimoto, Richard I. ;
Dillin, Andrew ;
Kelly, Jeffery W. .
SCIENCE, 2008, 319 (5865) :916-919
[5]   TDP-43: the relationship between protein aggregation and neurodegeneration in amyotrophic lateral sclerosis and frontotemporal lobar degeneration [J].
Baloh, Robert H. .
FEBS JOURNAL, 2011, 278 (19) :3539-3549
[6]   Staufen- and FMRP-containing neuronal RNPs are structurally and functionally related to somatic P bodies [J].
Barbee, Scott A. ;
Estes, Patricia S. ;
Cziko, Anne-Marie ;
Hillebrand, Jens ;
Luedeman, Rene A. ;
Coller, Jeff M. ;
Johnson, Nick ;
Howlett, Iris C. ;
Geng, Cuiyun ;
Ueda, Ryu ;
Brand, Andrea H. ;
Newbury, Sarah F. ;
Wilhelm, James E. ;
Levine, Richard B. ;
Nakamura, Akira ;
Parker, Roy ;
Ramaswami, Mani .
NEURON, 2006, 52 (06) :997-1009
[7]   Neuronal mRNAs travel singly into dendrites [J].
Batish, Mona ;
van den Bogaard, Patrick ;
Kramer, Fred Russell ;
Tyagi, Sanjay .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (12) :4645-4650
[8]   Model Organisms Reveal Insight into Human Neurodegenerative Disease: Ataxin-2 Intermediate-Length Polyglutamine Expansions Are a Risk Factor for ALS [J].
Bonini, Nancy M. ;
Gitler, Aaron D. .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2011, 45 (03) :676-683
[9]   Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy [J].
Brais, B ;
Bouchard, JP ;
Xie, YG ;
Rochefort, DL ;
Chrétien, N ;
Tomé, FMS ;
Lafrenière, RG ;
Rommens, JM ;
Uyama, E ;
Nohira, O ;
Blumen, S ;
Korcyn, AD ;
Heutink, P ;
Mathieu, J ;
Duranceau, A ;
Codère, F ;
Fardeau, M ;
Rouleau, GA .
NATURE GENETICS, 1998, 18 (02) :164-167
[10]   Prion-like transmission of protein aggregates in neurodegenerative diseases [J].
Brundin, Patrik ;
Melki, Ronald ;
Kopito, Ron .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2010, 11 (04) :301-307