4.6 Article

Sex- and caste-specific transcriptomes of larval honey bee (Apis mellifera L.) gonads: DMRT A2 and Hsp83 are differentially expressed and regulated by juvenile hormone

期刊

INSECT MOLECULAR BIOLOGY
卷 31, 期 5, 页码 593-608

出版社

WILEY
DOI: 10.1111/imb.12782

关键词

differential gene expression; ovary; RNA-seq; social insect; testis

资金

  1. Department of Livestock Population Genomics, Institute of Animal Science, University of Hohenheim, Stuttgart, Germany
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - Brasil (CAPES) [001]
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [303401/2014-1]
  4. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [2017/25004-0, 2016/16622-9]

向作者/读者索取更多资源

In this study, a comparative RNA-seq analysis was conducted on the larval gonads of honey bees at a critical stage of development. Differential gene expression was identified among the three sex and caste phenotypes, with enrichment in metabolism, protein or ion binding, and oxidoreductase activity. The analysis also revealed metabolic pathways as enriched. Despite programmed cell death in worker ovaries, the transcriptomes of queen and worker ovaries showed higher similarity compared to drone testis. RT-qPCR analysis identified DMRT A2 and Hsp83 as potential molecular markers for sex- and caste-specific gonad development in honey bees due to their upregulation in response to juvenile hormone.
The gonads of honey bee, Apis mellifera, queens and drones are each composed of hundreds of serial units, the ovarioles and testioles, while the ovaries of the adult subfertile workers consist of only few ovarioles. We performed a comparative RNA-seq analysis on early fifth-instar (L5F1) larval gonads, which is a critical stage in gonad development of honey bee larvae. A total of 1834 genes were identified as differentially expressed (Padj < 0.01) among the three sex and caste phenotypes. The Gene Ontology analysis showed significant enrichment for metabolism, protein or ion binding, and oxidoreductase activity, and a KEGG analysis revealed metabolic pathways as enriched. In a principal component analysis for the total transcriptomes and hierarchical clustering of the DEGs, we found higher similarity between the queen and worker ovary transcriptomes compared to the drone testis, despite the onset of programmed cell death in the worker ovaries. Four DEGs were selected for RT-qPCR analyses, including their response to juvenile hormone (JH), which is a critical factor in the caste-specific development of the ovaries. Among these, DMRT A2 and Hsp83 were found upregulated by JH and, thus, emerged as potential molecular markers for sex- and caste-specific gonad development in honey bees.

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