Document Detail


The worker honeybee fat body proteome is extensively remodeled preceding a major life-history transition.
MedLine Citation:
PMID:  21969861     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Honeybee workers are essentially sterile female helpers that make up the majority of individuals in a colony. Workers display a marked change in physiology when they transition from in-nest tasks to foraging. Recent technological advances have made it possible to unravel the metabolic modifications associated with this transition. Previous studies have revealed extensive remodeling of brain, thorax, and hypopharyngeal gland biochemistry. However, data on changes in the abdomen is scarce. To narrow this gap we investigated the proteomic composition of abdominal tissue in the days typically preceding the onset of foraging in honeybee workers. In order to get a broader representation of possible protein dynamics, we used workers of two genotypes with differences in the age at which they initiate foraging. This approach was combined with RNA interference-mediated downregulation of an insulin/insulin-like signaling component that is central to foraging behavior, the insulin receptor substrate (irs), and with measurements of glucose and lipid levels. Our data provide new insight into the molecular underpinnings of phenotypic plasticity in the honeybee, invoke parallels with vertebrate metabolism, and support an integrated and irs-dependent association of carbohydrate and lipid metabolism with the transition from in-nest tasks to foraging.
Authors:
Queenie W T Chan; Navdeep S Mutti; Leonard J Foster; Sarah D Kocher; Gro V Amdam; Florian Wolschin
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2011-09-28
Journal Detail:
Title:  PloS one     Volume:  6     ISSN:  1932-6203     ISO Abbreviation:  PLoS ONE     Publication Date:  2011  
Date Detail:
Created Date:  2011-10-04     Completed Date:  2012-04-13     Revised Date:  2012-05-07    
Medline Journal Info:
Nlm Unique ID:  101285081     Medline TA:  PLoS One     Country:  United States    
Other Details:
Languages:  eng     Pagination:  e24794     Citation Subset:  IM    
Affiliation:
Centre for High-Throughput Biology and Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada.
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MeSH Terms
Descriptor/Qualifier:
Abdomen / physiology
Animals
Bees / genetics*,  physiology*
Carbohydrates / chemistry
Down-Regulation
Female
Gene Expression Regulation*
Genotype
Glucose / metabolism
Insulin / metabolism
Lipid Metabolism
Lipids / chemistry
Models, Genetic
Phenotype
Proteome
Proteomics / methods*
RNA Interference
RNA, Double-Stranded / metabolism
RNA, Messenger / metabolism
Grant Support
ID/Acronym/Agency:
P01 AG22500/AG/NIA NIH HHS
Chemical
Reg. No./Substance:
0/Carbohydrates; 0/Insulin; 0/Lipids; 0/Proteome; 0/RNA, Double-Stranded; 0/RNA, Messenger; 50-99-7/Glucose
Comments/Corrections

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