PKG and NHR-49 signalling co-ordinately regulate short-term fasting-induced lysosomal lipid accumulation in C. elegans

Biochemical Journal

Volumn 461, Issue 3, 2014, Pages 209-520

  Huang, Wen Ming ^a   Li, Zhao Yu ^a   Xu, Yan Jun ^a   Wang, Wei ^a   Zhou, Mao Ge ^b   Zhang, Peng ^b   Liu, Ping Sheng ^b   Xu, Tao ^a,b   Wu, Zheng Xing ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

^b INSTITUTE OF BIOPHYSICS   (China)

Author keywords

Caenorhabditis elegans; Cyclic GMP dependent protein kinase; Lysosomal lipid; Nuclear hormone receptor 49 (NHR 49); Stress response

Indexed keywords

CAENORHABDITIS ELEGANS PROTEIN; CALCIUM INDEPENDENT PHOSPHOLIPASE A2; CYCLIC GMP DEPENDENT PROTEIN KINASE; DAF 3 PROTEIN; EGL 4 PROTEIN; HORMONE RECEPTOR; HYDROLASE; LIPID; NUCLEAR HORMONE RECEPTOR 49; RAB7 PROTEIN; SMAD PROTEIN; UNCLASSIFIED DRUG; CELL RECEPTOR; DAF 3 PROTEIN, C ELEGANS; DAF-3 PROTEIN, C ELEGANS; EGL 4 PROTEIN, C ELEGANS; EGL-4 PROTEIN, C ELEGANS; NERVE PROTEIN; NHR 49 PROTEIN, C ELEGANS; NHR-49 PROTEIN, C ELEGANS;

ANIMAL TISSUE; ARTICLE; AUTOPHAGY; CAENORHABDITIS ELEGANS; CONTROLLED STUDY; CYTOPLASM; DIET RESTRICTION; ENDOCYTOSIS; LIPID STORAGE; LYSOSOME; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; SENSORY NERVE CELL; SHORT TERM FASTING; SIGNAL TRANSDUCTION; ANIMAL; CHEMISTRY; COMPARATIVE STUDY; DRUG ANTAGONISM; DRUG POTENTIATION; ENZYME ACTIVATION; ENZYMOLOGY; GENETICS; KINETICS; LIPID METABOLISM; METABOLISM; MUTATION; PHYSIOLOGICAL STRESS; PHYSIOLOGY; RNA INTERFERENCE; SENSORY RECEPTOR; TRANSGENIC ANIMAL; ULTRASTRUCTURE; UPREGULATION;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; CYCLIC GMP-DEPENDENT PROTEIN KINASES; ENZYME ACTIVATION; FASTING; HYDROLASES; KINETICS; LIPID METABOLISM; LYSOSOMES; MUTATION; NERVE TISSUE PROTEINS; PHOSPHOLIPASES A2, CALCIUM-INDEPENDENT; RECEPTORS, CYTOPLASMIC AND NUCLEAR; RNA INTERFERENCE; SENSORY RECEPTOR CELLS; SIGNAL TRANSDUCTION; SMAD PROTEINS; STRESS, PHYSIOLOGICAL; UP-REGULATION;

EID: 84904128472     PISSN: 02646021     EISSN: 14708728     Source Type: Journal    
DOI: 10.1042/BJ20140191     Document Type: Article

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