Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules
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-transcriptiona...
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creator | Aulas, Anaïs Fay, Marta M. Szaflarski, Witold Kedersha, Nancy Anderson, Paul Ivanov, Pavel |
description | 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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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.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/55656</identifier><identifier>PMID: 28570526</identifier><language>eng</language><publisher>United States: MyJove Corporation</publisher><subject>Cell Culture Techniques ; Cell Line, Tumor ; Cellular Biology ; Cytoplasmic Granules ; Humans ; Protein Biosynthesis ; RNA, Messenger ; RNA-Binding Proteins ; Stress, Physiological</subject><ispartof>Journal of Visualized Experiments, 2017-05 (123)</ispartof><rights>Copyright © 2017, Journal of Visualized Experiments</rights><rights>Copyright © 2017, Journal of Visualized Experiments 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c382t-80312912c63e6c42774d2885cc3ab496950e6daf321e967c0f33f5a90eb306793</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://www.jove.com/files/email_thumbs/55656.png</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607937/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607937/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,3844,27928,27929,53795,53797</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.3791/55656$$EView_record_in_Journal_of_Visualized_Experiments$$FView_record_in_$$GJournal_of_Visualized_Experiments</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28570526$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aulas, Anaïs</creatorcontrib><creatorcontrib>Fay, Marta M.</creatorcontrib><creatorcontrib>Szaflarski, Witold</creatorcontrib><creatorcontrib>Kedersha, Nancy</creatorcontrib><creatorcontrib>Anderson, Paul</creatorcontrib><creatorcontrib>Ivanov, Pavel</creatorcontrib><title>Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules</title><title>Journal of Visualized Experiments</title><addtitle>J Vis Exp</addtitle><description>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.</description><subject>Cell Culture Techniques</subject><subject>Cell Line, Tumor</subject><subject>Cellular Biology</subject><subject>Cytoplasmic Granules</subject><subject>Humans</subject><subject>Protein Biosynthesis</subject><subject>RNA, Messenger</subject><subject>RNA-Binding Proteins</subject><subject>Stress, Physiological</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE9LAzEQxYMottZ-AQ-Si-BlNX-aZHMRymKr0OJBBW8hzWZtyu6mJruFfntXW0s9zQzze2-GB8AQozsqJL5njDN-AvpYjlCCUvFxetT3wEWMK4Q4QSw9Bz2SMoEY4X0wnttm6fMIGw-zUsfoii3Mto1fd0PlDJx446COcK6rSpdO1_C1CTZGOA26bksbL8FZoctoh_s6AO-Tx7fsKZm9TJ-z8SwxNCVNkiKKicTEcGq5GREhRjlJU2YM1YuR5JIhy3NdUIKt5MKggtKCaYnsgiIuJB2Ah53vul1UNje2boIu1Tq4Soet8tqp_5vaLdWn3yjGUScXncHt3iD4r9bGRlUuGluWura-jQpLxARlXKYderNDTfAxBlsczmCkfuJWv3F33PXxTwfqL98OuNoBK7-xauXbUHcZ7dXfi0mCRg</recordid><startdate>20170512</startdate><enddate>20170512</enddate><creator>Aulas, Anaïs</creator><creator>Fay, Marta M.</creator><creator>Szaflarski, Witold</creator><creator>Kedersha, Nancy</creator><creator>Anderson, Paul</creator><creator>Ivanov, Pavel</creator><general>MyJove Corporation</general><scope>ALOKQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170512</creationdate><title>Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules</title><author>Aulas, Anaïs ; Fay, Marta M. ; Szaflarski, Witold ; Kedersha, Nancy ; Anderson, Paul ; Ivanov, Pavel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-80312912c63e6c42774d2885cc3ab496950e6daf321e967c0f33f5a90eb306793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cell Culture Techniques</topic><topic>Cell Line, Tumor</topic><topic>Cellular Biology</topic><topic>Cytoplasmic Granules</topic><topic>Humans</topic><topic>Protein Biosynthesis</topic><topic>RNA, Messenger</topic><topic>RNA-Binding Proteins</topic><topic>Stress, Physiological</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aulas, Anaïs</creatorcontrib><creatorcontrib>Fay, Marta M.</creatorcontrib><creatorcontrib>Szaflarski, Witold</creatorcontrib><creatorcontrib>Kedersha, Nancy</creatorcontrib><creatorcontrib>Anderson, Paul</creatorcontrib><creatorcontrib>Ivanov, Pavel</creatorcontrib><collection>JoVE Journal: Biology</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Visualized Experiments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Aulas, Anaïs</au><au>Fay, Marta M.</au><au>Szaflarski, Witold</au><au>Kedersha, Nancy</au><au>Anderson, Paul</au><au>Ivanov, Pavel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules</atitle><jtitle>Journal of Visualized Experiments</jtitle><addtitle>J Vis Exp</addtitle><date>2017-05-12</date><risdate>2017</risdate><issue>123</issue><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>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.</abstract><cop>United States</cop><pub>MyJove Corporation</pub><pmid>28570526</pmid><doi>10.3791/55656</doi><oa>free_for_read</oa></addata></record> |
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subjects | Cell Culture Techniques Cell Line, Tumor Cellular Biology Cytoplasmic Granules Humans Protein Biosynthesis RNA, Messenger RNA-Binding Proteins Stress, Physiological |
title | Methods to Classify Cytoplasmic Foci as Mammalian Stress Granules |
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