4.4 Article

Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules

Journal

JOVE-JOURNAL OF VISUALIZED EXPERIMENTS
Volume -, Issue 123, Pages -

Publisher

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/55656

Keywords

Cellular Biology; Issue 123; RNA granules; stress granules; mRNA; translation repression; immunostaining; in situ hybridization; stress response

Funding

  1. National Institutes of Health [GM111700, CA168872, NS094918]
  2. National Science Centre in Poland [UMO-2012/06/M/NZ3/00054]
  3. Ministry of Science and Higher Education in Poland
  4. Polish-American Fulbright Commission

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Cells are often challenged by sudden environmental changes. Stress Granules (SGs), cytoplasmic ribonucleoprotein complexes that form in cells exposed to stress conditions, are implicated in various aspects of cell metabolism and survival. SGs modulate cellular signaling pathways, post-transcriptional gene expression, and stress response programs. The formation of these mRNA-containing granules is directly connected to cellular translation. SG assembly is triggered by inhibited translation initiation, and SG disassembly is promoted by translation activation or by inhibited translation elongation. This relationship is further highlighted by SG composition. Core SG components are stalled translation pre-initiation complexes, mRNA, and selected RNA-binding Proteins (RBPs). The purpose of SG assembly is to conserve cellular energy by sequestering translationally stalled housekeeping mRNAs, allowing for the enhanced translation of stress-responsive proteins. In addition to the core constituents, such as stalled translation preinitiation complexes, SGs contain a plethora of other proteins and signaling molecules. Defects in SG formation can impair cellular adaptation to stress and can thus promote cell death. SGs and similar RNA-containing granules have been linked to a number of human diseases, including neurodegenerative disorders and cancer, leading to the recent interest in classifying and defining RNA granule subtypes. This protocol describes assays to characterize and quantify mammalian SGs.

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