Measurements of Physiological Stress Responses in C. Elegans

被引:21
作者
Bar-Ziv, Raz [1 ]
Frakes, Ashley E. [1 ]
Higuchi-Sanabria, Ryo [1 ]
Bolas, Theodore [1 ]
Frankino, Phillip A. [1 ]
Gildea, Holly K. [1 ]
Metcalf, Melissa G. [1 ]
Dillin, Andrew [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2020年 / 159期
基金
美国国家科学基金会;
关键词
Biology; Issue; 159; stress; C; elegans; unfolded protein response; endoplasmic reticulum; mitochondria; heat shock response; transcriptional reporter; oxidative stress; protein homeostasis; TISSUE-SPECIFIC ACTIVITIES; UNFOLDED PROTEIN RESPONSE; HEAT-SHOCK RESPONSE; CAENORHABDITIS-ELEGANS; LIFE-SPAN; DAF-16; THERMOTOLERANCE; ACTIVATION; LONGEVITY; GENES;
D O I
10.3791/61001
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organisms are often exposed to fluctuating environments and changes in intracellular homeostasis, which can have detrimental effects on their proteome and physiology. Thus, organisms have evolved targeted and specific stress responses dedicated to repair damage and maintain homeostasis. These mechanisms include the unfolded protein response of the endoplasmic reticulum (UPRER), the unfolded protein response of the mitochondria (UPRMT), the heat shock response (HSR), and the oxidative stress response (OxSR). The protocols presented here describe methods to detect and characterize the activation of these pathways and their physiological consequences in the nematode, C. elegans. First, the use of pathway-specific fluorescent transcriptional reporters is described for rapid cellular characterization, drug screening, or large-scale genetic screening (e.g., RNAi or mutant libraries). In addition, complementary, robust physiological assays are described, which can be used to directly assess sensitivity of animals to specific stressors, serving as functional validation of the transcriptional reporters. Together, these methods allow for rapid characterization of the cellular and physiological effects of internal and external proteotoxic perturbations.
引用
收藏
页码:1 / 21
页数:21
相关论文
共 61 条
  • [1] Regulation of the Caenorhabditis elegans oxidative stress defense protein SKN-1 by glycogen synthase kinase-3
    An, JH
    Vranas, K
    Lucke, M
    Inoue, H
    Hisamoto, N
    Matsumoto, K
    Blackwell, TK
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (45) : 16275 - 16280
  • [2] HSF-1-mediated cytoskeletal integrity determines thermotolerance and life span
    Baird, Nathan A.
    Douglas, Peter M.
    Simic, Milos S.
    Grant, Ana R.
    Moresco, James J.
    Wolff, Suzanne C.
    Yates, John R., III
    Manning, Gerard
    Dillin, Andrew
    [J]. SCIENCE, 2014, 346 (6207) : 360 - 363
  • [3] Mitochondrial protein quality control during biogenesis and aging
    Baker, Brooke M.
    Haynes, Cole M.
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2011, 36 (05) : 254 - 261
  • [4] SKN-1/Nrf, stress responses, and aging in Caenorhabditis elegans
    Blackwell, T. Keith
    Steinbaugh, Michael J.
    Hourihan, John M.
    Ewald, Collin Y.
    Isik, Meltem
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2015, 88 : 290 - 301
  • [5] BRENNER S, 1974, GENETICS, V77, P71
  • [6] IRE1 couples endoplasmic reticulum load to secretory capacity by processing the XBP-1 mRNA
    Calfon, M
    Zeng, HQ
    Urano, F
    Till, JH
    Hubbard, SR
    Harding, HP
    Clark, SG
    Ron, D
    [J]. NATURE, 2002, 415 (6867) : 92 - 96
  • [7] Mitochondria are a major source of paraquat-induced reactive oxygen species production in the brain
    Castello, Pablo R.
    Drechsel, Derek A.
    Patel, Manisha
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (19) : 14186 - 14193
  • [8] Regulators of oxidative stress response genes in Escherichia coli and their functional conservation in bacteria
    Chiang, Sarah M.
    Schellhorn, Herb E.
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2012, 525 (02) : 161 - 169
  • [9] The WD40 Repeat Protein WDR-23 Functions with the CUL4/DDB1 Ubiquitin Ligase To Regulate Nuclear Abundance and Activity of SKN-1 in Caenorhabditis elegans
    Choe, Keith P.
    Przybysz, Aaron J.
    Strange, Kevin
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2009, 29 (10) : 2704 - 2715
  • [10] Daniele J.R., 2018, BIORXIV471177, DOI [10.1101/471177, DOI 10.1101/471177]