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应激颗粒转录组揭示了应激颗粒中mRNA积累的原理。

The Stress Granule Transcriptome Reveals Principles of mRNA Accumulation in Stress Granules.

作者信息

Khong Anthony, Matheny Tyler, Jain Saumya, Mitchell Sarah F, Wheeler Joshua R, Parker Roy

机构信息

Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA; Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA.

Department of Chemistry and Biochemistry, University of Colorado, Boulder, CO 80309, USA.

出版信息

Mol Cell. 2017 Nov 16;68(4):808-820.e5. doi: 10.1016/j.molcel.2017.10.015. Epub 2017 Nov 9.

Abstract

Stress granules are mRNA-protein assemblies formed from nontranslating mRNAs. Stress granules are important in the stress response and may contribute to some degenerative diseases. Here, we describe the stress granule transcriptome of yeast and mammalian cells through RNA-sequencing (RNA-seq) analysis of purified stress granule cores and single-molecule fluorescence in situ hybridization (smFISH) validation. While essentially every mRNA, and some noncoding RNAs (ncRNAs), can be targeted to stress granules, the targeting efficiency varies from <1% to >95%. mRNA accumulation in stress granules correlates with longer coding and UTR regions and poor translatability. Quantifying the RNA-seq analysis by smFISH reveals that only 10% of bulk mRNA molecules accumulate in mammalian stress granules and that only 185 genes have more than 50% of their mRNA molecules in stress granules. These results suggest that stress granules may not represent a specific biological program of messenger ribonucleoprotein (mRNP) assembly, but instead form by condensation of nontranslating mRNPs in proportion to their length and lack of association with ribosomes.

摘要

应激颗粒是由非翻译mRNA形成的mRNA-蛋白质聚集体。应激颗粒在应激反应中很重要,可能与某些退行性疾病有关。在这里,我们通过对纯化的应激颗粒核心进行RNA测序(RNA-seq)分析和单分子荧光原位杂交(smFISH)验证,描述了酵母和哺乳动物细胞的应激颗粒转录组。虽然基本上每个mRNA以及一些非编码RNA(ncRNA)都可以靶向应激颗粒,但靶向效率从小于1%到大于95%不等。应激颗粒中的mRNA积累与较长的编码区和UTR区域以及较差的可翻译性相关。通过smFISH对RNA-seq分析进行定量显示,只有10%的大量mRNA分子积聚在哺乳动物应激颗粒中,并且只有185个基因的mRNA分子有超过50%存在于应激颗粒中。这些结果表明,应激颗粒可能并不代表信使核糖核蛋白(mRNP)组装的特定生物学程序,而是由非翻译mRNP根据其长度和与核糖体的缺乏关联程度通过凝聚形成的。

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