Granules harboring translationally active mRNAs provide a platform for P-body formation following stress.
Granules harboring translationally active mRNAs provide a platform for P-body formation following stress.
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DOI:
10.1016/j.celrep.2014.09.040
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发表时间:
2014-11-06
期刊:
影响因子:
8.8
通讯作者:
Ashe MP
中科院分区:
文献类型:
--
作者:
Lui J;Castelli LM;Pizzinga M;Simpson CE;Hoyle NP;Bailey KL;Campbell SG;Ashe MP
The localization of mRNA to defined cytoplasmic sites in eukaryotic cells not only allows localized protein production but also determines the fate of mRNAs. For instance, translationally repressed mRNAs localize to P-bodies and stress granules where their decay and storage, respectively, are directed. Here, we find that several mRNAs are localized to granules in unstressed, actively growing cells. These granules play a key role in the stress-dependent formation of P-bodies. Specific glycolytic mRNAs are colocalized in multiple granules per cell, which aggregate during P-body formation. Such aggregation is still observed under conditions or in mutants where P-bodies do not form. In unstressed cells, the mRNA granules appear associated with active translation; this might enable a coregulation of protein expression from the same pathways or complexes. Parallels can be drawn between this coregulation and the advantage of operons in prokaryotic systems. Specific mRNAs are localized to cytoplasmic granules in actively growing cells After stress, the granules serve as a platform for P-body formation Certain glycolytic mRNAs colocalize and are translated in cytoplasmic granules Translation of functionally related mRNAs may be coregulated in the granules Lui et al. show that specific mRNAs localize to granules in actively growing cells. These mRNA granules are associated with active translation and are proposed to allow coregulation of protein expression from the same pathway or complex. Following stress, the granules aggregate to drive the formation of P-bodies.