Polygenic control of Caenorhabditis elegans fat storage

2006 ◽  
Vol 38 (3) ◽  
pp. 363-368 ◽  
Author(s):  
Ho Yi Mak ◽  
Laura S Nelson ◽  
Michael Basson ◽  
Carl D Johnson ◽  
Gary Ruvkun
2011 ◽  
Vol 411 (3) ◽  
pp. 537-553 ◽  
Author(s):  
Jun Zhang ◽  
Razan Bakheet ◽  
Ranjit S. Parhar ◽  
Cheng-Han Huang ◽  
M. Mahmood Hussain ◽  
...  

2015 ◽  
Vol 211 (2) ◽  
pp. 261-271 ◽  
Author(s):  
Vineet Choudhary ◽  
Namrata Ojha ◽  
Andy Golden ◽  
William A. Prinz

Lipid droplets (LDs) are found in all cells and play critical roles in lipid metabolism. De novo LD biogenesis occurs in the endoplasmic reticulum (ER) but is not well understood. We imaged early stages of LD biogenesis using electron microscopy and found that nascent LDs form lens-like structures that are in the ER membrane, raising the question of how these nascent LDs bud from the ER as they grow. We found that a conserved family of proteins, fat storage-inducing transmembrane (FIT) proteins, is required for proper budding of LDs from the ER. Elimination or reduction of FIT proteins in yeast and higher eukaryotes causes LDs to remain in the ER membrane. Deletion of the single FIT protein in Caenorhabditis elegans is lethal, suggesting that LD budding is an essential process in this organism. Our findings indicated that FIT proteins are necessary to promote budding of nascent LDs from the ER.


2014 ◽  
Vol 28 (S1) ◽  
Author(s):  
Mack Shay ◽  
Marwa Al‐Tameemi ◽  
Saxon Wright ◽  
Robert McLean ◽  
Dhiraj Vattem ◽  
...  

PLoS ONE ◽  
2010 ◽  
Vol 5 (3) ◽  
pp. e9869 ◽  
Author(s):  
Bin Liang ◽  
Kim Ferguson ◽  
Lisa Kadyk ◽  
Jennifer L. Watts

PLoS Biology ◽  
2009 ◽  
Vol 7 (3) ◽  
pp. e1000060 ◽  
Author(s):  
Kevin T Jones ◽  
Elisabeth R Greer ◽  
David Pearce ◽  
Kaveh Ashrafi

2019 ◽  
Vol 10 (1) ◽  
pp. 189-198 ◽  
Author(s):  
Isaiah A. A. Neve ◽  
Jessica N. Sowa ◽  
Chih-Chun J. Lin ◽  
Priya Sivaramakrishnan ◽  
Christophe Herman ◽  
...  

The relationship of genotypes to phenotypes can be modified by environmental inputs. Such crucial environmental inputs include metabolic cues derived from microbes living together with animals. Thus, the analysis of genetic effects on animals’ physiology can be confounded by variations in the metabolic profile of microbes. Caenorhabditis elegans exposed to distinct bacterial strains and species exhibit phenotypes different at cellular, developmental, and behavioral levels. Here we reported metabolomic profiles of three Escherichia coli strains, B strain OP50, K-12 strain MG1655, and B-K-12 hybrid strain HB101, as well as different mitochondrial and fat storage phenotypes of C. elegans exposed to MG1655 and HB101 vs. OP50. We found that these metabolic phenotypes of C. elegans are not correlated with overall metabolic patterning of bacterial strains, but their specific metabolites. In particular, the fat storage phenotype is traced to the betaine level in different bacterial strains. HT115 is another K-12 E. coli strain that is commonly utilized to elicit an RNA interference response, and we showed that C. elegans exposed to OP50 and HT115 exhibit differences in mitochondrial morphology and fat storage levels. We thus generated an RNA interference competent OP50 (iOP50) strain that can robustly and consistently knockdown endogenous C. elegans genes in different tissues. Together, these studies suggest the importance of specific bacterial metabolites in regulating the host’s physiology and provide a tool to prevent confounding effects when analyzing genotype-phenotype interactions under different bacterial backgrounds.


PLoS ONE ◽  
2010 ◽  
Vol 5 (9) ◽  
pp. e12810 ◽  
Author(s):  
Kelvin Yen ◽  
Thuc T. Le ◽  
Ankita Bansal ◽  
Sri Devi Narasimhan ◽  
Ji-Xin Cheng ◽  
...  

2019 ◽  
Author(s):  
Isaiah A. A. Neve ◽  
Jessica N. Sowa ◽  
Chih-Chun J. Lin ◽  
Priya Sivaramakrishnan ◽  
Christophe Herman ◽  
...  

AbstractThe relationship of genotypes to phenotypes can be modified by environmental inputs. Such crucial environmental inputs include metabolic cues derived from microbes living together with animals. Thus the analysis of genetic effects on animals’ physiology can be confounded by variations in the metabolic profile of microbes. Caenorhabditis elegans exposed to distinct bacterial strains and species exhibit phenotypes different at cellular, developmental and behavioral levels. Here we reported metabolomic profiles of three Escherichia coli strains, B strain OP50, K-12 strain MG1655, and B-K-12 hybrid strain HB101, and also different mitochondrial and fat storage phenotypes of C. elegans exposed to MG1655 and HB101 versus OP50. We found that these metabolic phenotypes of C. elegans are not correlated with overall metabolic patterning of bacterial strains, but their specific metabolites. In particular, the fat storage phenotype is traced to the betaine level in different bacterial strains. HT115 is another K-12 E. coli strain that is commonly utilized to elicit an RNA interference response, and we showed that C. elegans exposed to OP50 and HT115 exhibit differences in mitochondrial morphology and fat storage levels. We thus generated an RNA interference competent OP50 (iOP50) strain that can robustly and consistently knockdown endogenous C. elegans genes in different tissues. Together, these studies suggest the importance of specific bacterial metabolites in regulating the host’s physiology, and provide a tool to prevent confounding effects when analyzing genotype-phenotype interactions under different bacterial backgrounds.


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