Relationship of GW/P-Bodies with Stress Granules

被引:86
|
作者
Stoecklin, Georg [1 ]
Kedersha, Nancy [2 ,3 ]
机构
[1] DKFZ ZMBH Alliance, German Canc Res Ctr DKFZ, Helmholtz Jr Res Grp Posttranscript Control Gene, D-69120 Heidelberg, Germany
[2] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
MESSENGER-RNA DECAY; MICRORNA-DEPENDENT LOCALIZATION; CYTOPLASMIC PROCESSING BODIES; MENTAL-RETARDATION PROTEIN; P-BODY FORMATION; SACCHAROMYCES-CEREVISIAE; BINDING-PROTEIN; HUMAN-CELLS; HEAT-SHOCK; TRANSLATION INITIATION;
D O I
10.1007/978-1-4614-5107-5_12
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
Whereas P-bodies are intimately linked to the cytoplasmic RNA decay machinery, stress granules harbor stalled translation initiation complexes that accumulate upon stress-induced translation arrest. In this Chapter, we reflect on the relationship between P-bodies and stress granules. In mammalian cells, the two structures can be clearly distinguished from each other using specific protein or RNA markers, but they also share many proteins and mRNAs. While the formation of P-bodies and stress granules is coordinately triggered by stress, their assembly appears to be regulated independently by different pathways. Under certain types of stress, P-bodies frequently dock with stress granules, and overexpressing certain proteins that localize to both structures can cause P-body/stress granule fusion. Currently available data suggest that these self-assembling compartments are controlled by flux of mRNAs within the cytoplasm, and that their assembly mirrors the translation and degradation rates of their component mRNAs.
引用
收藏
页码:197 / 211
页数:15
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