Literature DB >> 20591854

Insulin receptor substrate influences female caste development in honeybees.

Florian Wolschin1, Navdeep S Mutti, Gro V Amdam.   

Abstract

The insulin/insulin-like signalling (IIS) network is conserved among animals and is central to growth and development. In eusocial honeybees (Apis mellifera), IIS is hypothesized to shape female caste fate. We tested this hypothesis via RNA interference (RNAi) knockdown of the insulin receptor substrate (IRS) homologue, a key adaptor protein in IIS. Female larvae naturally develop into queens (reproductives) or workers (helpers) after being fed rich versus limited diets, respectively. Feeding larvae a rich diet mixed with dsRNA (double stranded RNA) targeting irs gene transcript decreased irs mRNA abundance and caused development of worker morphology. Controls receiving rich larval diet and control dsRNA developed queen morphology. Whole-body mass spectrometry profiling of larvae collected 72, 96 and 120 h after dsRNA treatments revealed proteomic differences between irs gene knockdowns and controls, including levels of hexamerin 110, a storage protein connected to natural caste differences.

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Year:  2010        PMID: 20591854      PMCID: PMC3030871          DOI: 10.1098/rsbl.2010.0463

Source DB:  PubMed          Journal:  Biol Lett        ISSN: 1744-9561            Impact factor:   3.703


  18 in total

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  28 in total

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Authors:  Navdeep S Mutti; Adam G Dolezal; Florian Wolschin; Jasdeep S Mutti; Kulvinder S Gill; Gro V Amdam
Journal:  J Exp Biol       Date:  2011-12-01       Impact factor: 3.312

2.  Insulin-like peptides (AmILP1 and AmILP2) differentially affect female caste development in the honey bee (Apis mellifera L.).

Authors:  Ying Wang; Sergio V Azevedo; Klaus Hartfelder; Gro V Amdam
Journal:  J Exp Biol       Date:  2013-08-30       Impact factor: 3.312

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7.  The worker honeybee fat body proteome is extensively remodeled preceding a major life-history transition.

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8.  Honey bee PTEN--description, developmental knockdown, and tissue-specific expression of splice-variants correlated with alternative social phenotypes.

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