Suppr超能文献

通过多核糖体谱分析应激条件下的翻译起始

Analysis of translation initiation during stress conditions by polysome profiling.

作者信息

Coudert Laëtitia, Adjibade Pauline, Mazroui Rachid

机构信息

Department of Molecular Biology, Medical Biochemistry, and Pathology, Faculty of Medicine, Laval University; CHU de Quebec Research Center.

Department of Molecular Biology, Medical Biochemistry, and Pathology, Faculty of Medicine, Laval University; CHU de Quebec Research Center;

出版信息

J Vis Exp. 2014 May 19(87):51164. doi: 10.3791/51164.

Abstract

Precise control of mRNA translation is fundamental for eukaryotic cell homeostasis, particularly in response to physiological and pathological stress. Alterations of this program can lead to the growth of damaged cells, a hallmark of cancer development, or to premature cell death such as seen in neurodegenerative diseases. Much of what is known concerning the molecular basis for translational control has been obtained from polysome analysis using a density gradient fractionation system. This technique relies on ultracentrifugation of cytoplasmic extracts on a linear sucrose gradient. Once the spin is completed, the system allows fractionation and quantification of centrifuged zones corresponding to different translating ribosomes populations, thus resulting in a polysome profile. Changes in the polysome profile are indicative of changes or defects in translation initiation that occur in response to various types of stress. This technique also allows to assess the role of specific proteins on translation initiation, and to measure translational activity of specific mRNAs. Here we describe our protocol to perform polysome profiles in order to assess translation initiation of eukaryotic cells and tissues under either normal or stress growth conditions.

摘要

精确控制mRNA翻译对于真核细胞的稳态至关重要,尤其是在应对生理和病理应激时。这一程序的改变会导致受损细胞的生长,这是癌症发展的一个标志,或者导致过早的细胞死亡,如在神经退行性疾病中所见。关于翻译控制分子基础的许多已知信息是通过使用密度梯度分级系统的多核糖体分析获得的。该技术依赖于在线性蔗糖梯度上对细胞质提取物进行超速离心。一旦离心完成,该系统允许对对应于不同翻译核糖体群体的离心区进行分级和定量,从而得到多核糖体图谱。多核糖体图谱的变化表明了响应各种类型应激时翻译起始的变化或缺陷。该技术还允许评估特定蛋白质在翻译起始中的作用,并测量特定mRNA的翻译活性。在这里,我们描述了我们进行多核糖体图谱分析的方案,以评估正常或应激生长条件下真核细胞和组织的翻译起始情况。

相似文献

2
Polysome analysis of mammalian cells.
Methods Enzymol. 2013;530:183-92. doi: 10.1016/B978-0-12-420037-1.00010-5.
3
4
Polysome profile analysis--yeast.
Methods Enzymol. 2013;530:173-81. doi: 10.1016/B978-0-12-420037-1.00009-9.
5
Measuring mRNA Translation by Polysome Profiling.
Methods Mol Biol. 2016;1421:127-35. doi: 10.1007/978-1-4939-3591-8_11.
6
Polysome analysis for determining mRNA and ribosome association in Saccharomyces cerevisiae.
Methods Enzymol. 2013;530:193-206. doi: 10.1016/B978-0-12-420037-1.00011-7.
7
Studying the Translatome with Polysome Profiling.
Methods Mol Biol. 2016;1358:59-69. doi: 10.1007/978-1-4939-3067-8_4.
8
Accessing the Human Pluripotent Stem Cell Translatome by Polysome Profiling.
Methods Mol Biol. 2022;2520:309-319. doi: 10.1007/7651_2021_437.
9
Polysome Profiling without Gradient Makers or Fractionation Systems.
J Vis Exp. 2021 Jun 1(172). doi: 10.3791/62680.

引用本文的文献

1
Functional Activities of Cohesin Proteins Can Be Altered by Chemical Chaperones.
Protein J. 2025 Jul 16. doi: 10.1007/s10930-025-10276-7.
2
Understanding the regulation of protein synthesis under stress conditions.
Biophys J. 2024 Oct 15;123(20):3627-3639. doi: 10.1016/j.bpj.2024.09.014. Epub 2024 Sep 14.
5
The ribosome quality control factor Asc1 determines the fate of HSP70 mRNA on and off the ribosome.
Nucleic Acids Res. 2023 Jul 7;51(12):6370-6388. doi: 10.1093/nar/gkad338.
6
Ribosomal Stress Couples with the Hypoxia Response in Dec1-Dependent Orthodontic Tooth Movement.
Int J Mol Sci. 2022 Dec 29;24(1):618. doi: 10.3390/ijms24010618.
7
Prostate cancer resistance leads to a global deregulation of translation factors and unconventional translation.
NAR Cancer. 2022 Nov 4;4(4):zcac034. doi: 10.1093/narcan/zcac034. eCollection 2022 Dec.
9
Polysome Profiling without Gradient Makers or Fractionation Systems.
J Vis Exp. 2021 Jun 1(172). doi: 10.3791/62680.
10
The RabGAP TBC-11 controls Argonaute localization for proper microRNA function in C. elegans.
PLoS Genet. 2021 Apr 7;17(4):e1009511. doi: 10.1371/journal.pgen.1009511. eCollection 2021 Apr.

本文引用的文献

1
Inactivation of the mTORC1-eukaryotic translation initiation factor 4E pathway alters stress granule formation.
Mol Cell Biol. 2013 Jun;33(11):2285-301. doi: 10.1128/MCB.01517-12. Epub 2013 Apr 1.
2
FMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brain.
PLoS One. 2013;8(3):e58296. doi: 10.1371/journal.pone.0058296. Epub 2013 Mar 7.
3
Characterization of fragile X mental retardation protein recruitment and dynamics in Drosophila stress granules.
PLoS One. 2013;8(2):e55342. doi: 10.1371/journal.pone.0055342. Epub 2013 Feb 7.
4
A novel function for the survival motoneuron protein as a translational regulator.
Hum Mol Genet. 2013 Feb 15;22(4):668-84. doi: 10.1093/hmg/dds474. Epub 2012 Nov 6.
6
A unifying model for mTORC1-mediated regulation of mRNA translation.
Nature. 2012 May 2;485(7396):109-13. doi: 10.1038/nature11083.
7
The chemotherapeutic agent bortezomib induces the formation of stress granules.
Cancer Cell Int. 2010 Apr 29;10:12. doi: 10.1186/1475-2867-10-12.
8
The mechanism of eukaryotic translation initiation and principles of its regulation.
Nat Rev Mol Cell Biol. 2010 Feb;11(2):113-27. doi: 10.1038/nrm2838.
9
Metazoan stress granule assembly is mediated by P-eIF2alpha-dependent and -independent mechanisms.
RNA. 2009 Oct;15(10):1814-21. doi: 10.1261/rna.1684009. Epub 2009 Aug 6.
10
Ribosomal footprints on a transcriptome landscape.
Genome Biol. 2009;10(4):215. doi: 10.1186/gb-2009-10-4-215. Epub 2009 Apr 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验