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      In-depth Proteome of the Hypopharyngeal Glands of Honeybee Workers Reveals Highly Activated Protein and Energy Metabolism in Priming the Secretion of Royal Jelly*

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          Abstract

          The hitherto depth proteomes of the hypopharyngeal glands (HGs) across the adult life of two stocks of honeybees with low (ITBs) and high royal jelly production (RJBs) uncover the molecular landscapes of the gland ontogeny and activity to match with gland age-specific tasks. Pathways involved in protein and energy metabolism are induced in HGs of RJB nurse bees to enhance royal jelly (RJ) secretion relative to ITBs. Our finding gains a novel mechanistic insight of the augment RJ-output in RJBs.

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          Highlights

          • In-depth proteome underpins the gland ontogeny and age-specific activity of the HGs.

          • The well-developed acini in the HGs of NBs promote the RJ secretary activities.

          • The enhanced protein and energy metabolism in the HGs boost the stronger RJ secretion of RJBs.

          Abstract

          Royal jelly (RJ) is a secretion of the hypopharyngeal glands (HGs) of honeybee workers. High royal jelly producing bees (RJBs), a stock of honeybees selected from Italian bees (ITBs), have developed a stronger ability to produce RJ than ITBs. However, the mechanism underpinning the high RJ-producing performance in RJBs is still poorly understood. We have comprehensively characterized and compared the proteome across the life span of worker bees between the ITBs and RJBs. Our data uncover distinct molecular landscapes that regulate the gland ontogeny and activity corresponding with age-specific tasks. Nurse bees (NBs) have a well-developed acini morphology and cytoskeleton of secretory cells in HGs to prime the gland activities of RJ secretion. In RJB NBs, pathways involved in protein synthesis and energy metabolism are functionally induced to cement the enhanced RJ secretion compared with ITBs. In behavior-manipulated RJB NBs, the strongly expressed proteins implicated in protein synthesis and energy metabolism further demonstrate their critical roles in the regulation of RJ secretion. Our findings provide a novel understanding of the mechanism consolidating the high RJ-output in RJBs.

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          Most cited references72

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          Genome-wide RNAi screen identifies human host factors crucial for influenza virus replication.

          Influenza A virus, being responsible for seasonal epidemics and reoccurring pandemics, represents a worldwide threat to public health. High mutation rates facilitate the generation of viral escape mutants, rendering vaccines and drugs directed against virus-encoded targets potentially ineffective. In contrast, targeting host cell determinants temporarily dispensable for the host but crucial for virus replication could prevent viral escape. Here we report the discovery of 287 human host cell genes influencing influenza A virus replication in a genome-wide RNA interference (RNAi) screen. Using an independent assay we confirmed 168 hits (59%) inhibiting either the endemic H1N1 (119 hits) or the current pandemic swine-origin (121 hits) influenza A virus strains, with an overlap of 60%. Notably, a subset of these common hits was also essential for replication of a highly pathogenic avian H5N1 strain. In-depth analyses of several factors provided insights into their infection stage relevance. Notably, SON DNA binding protein (SON) was found to be important for normal trafficking of influenza virions to late endosomes early in infection. We also show that a small molecule inhibitor of CDC-like kinase 1 (CLK1) reduces influenza virus replication by more than two orders of magnitude, an effect connected with impaired splicing of the viral M2 messenger RNA. Furthermore, influenza-virus-infected p27(-/-) (cyclin-dependent kinase inhibitor 1B; Cdkn1b) mice accumulated significantly lower viral titres in the lung, providing in vivo evidence for the importance of this gene. Thus, our results highlight the potency of genome-wide RNAi screening for the dissection of virus-host interactions and the identification of drug targets for a broad range of influenza viruses.
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            Regulation of honey bee division of labor by colony age demography

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              Pheromone communication in the honeybee (Apis mellifera L.).

              Recent studies have demonstrated a remarkable and unexpected complexity in social insect pheromone communication, particularly for honeybees (Apis mellifera L.). The intricate interactions characteristic of social insects demand a complex language, based on specialized chemical signals that provide a syntax that is deeper in complexity and richer in nuance than previously imagined. Here, we discuss this rapidly evolving field for honeybees, the only social insect for which any primer pheromones have been identified. Novel research has demonstrated the importance of complexity, synergy, context, and dose, mediated through spatial and temporal pheromone distribution, and has revealed an unprecedented wealth of identified semiochemicals and functions. These new results demand fresh terminology, and we propose adding "colony pheromone" and "passenger pheromone" to the current terms sociochemical, releaser, and primer pheromone to better encompass our growing understanding of chemical communication in social insects.
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                Author and article information

                Journal
                Mol Cell Proteomics
                Mol. Cell Proteomics
                mcprot
                mcprot
                MCP
                Molecular & Cellular Proteomics : MCP
                The American Society for Biochemistry and Molecular Biology
                1535-9476
                1535-9484
                April 2019
                7 January 2019
                7 January 2019
                : 18
                : 4
                : 606-621
                Affiliations
                [1]From the ‡ Institute of Apicultural Research/Key Laboratory of Pollinating Insect Biology, Ministry of Agriculture, Chinese Academy of Agricultural Sciences, No. 1 Beigou Xiangshan, Beijing, 100093, China
                Author notes
                § To whom correspondence should be addressed: Institute of Apicultural Research, Chinese Academy of Agricultural Sciences, No. 1 Beigou Xiangshan, Beijing, 100093, China. Tel.: 86-010-82106448; E-mail: apislijk@ 123456163.com .

                ¶ These authors contributed equally to this work.

                Author contributions: H.H. and J.L. designed research; H.H., M.F., Q.W., Y.F., and C.M. performed research; H.H., G.B., and L.M. analyzed data; H.H., G.B., and B.H. wrote the paper; X.Z., F.W., and L.M. contributed new reagents/analytic tools.

                Author information
                https://orcid.org/0000-0002-0687-8821
                Article
                RA118.001257
                10.1074/mcp.RA118.001257
                6442370
                30617159
                10cfc161-8a02-46d4-bed9-0df91405cfc1
                © 2019 Hu et al.

                Published by The American Society for Biochemistry and Molecular Biology, Inc.

                Author's Choice—Final version open access under the terms of the Creative Commons CC-BY license.

                History
                : 12 December 2018
                Funding
                Funded by: Agricultural Science and Technology Innovation Program, http://caas.net.cn/kxyj//kjcxgc/index.html#;
                Award ID: CAAS-ASTIP-2015-IAR
                Award Recipient :
                Funded by: Earmarked Fund for Modern Agro-industry Technology Research System, https://dx.doi.org/10.13039/501100009997;
                Award ID: CARS-44
                Award Recipient :
                Categories
                Research

                Molecular biology
                protein identification*,protein synthesis*,ribosomes*,molecular biology*,energy metabolism

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