Convergent Evolution Associated with the Loss of Developmental Diapause May Promote Extended Lifespan in Bees.
Abstract
Diapause has long been proposed to play a significant role in the evolution of eusociality in Hymenoptera. Recent studies have shown that shifts in the diapause stage precede social evolution in wasps and bees; however, the genomic basis remains unknown. Given the overlap in molecular pathways that regulate diapause and lifespan, we hypothesized that the evolutionary loss of developmental diapause may lead to extended lifespan among adults, which is a prerequisite for the evolution of eusociality. To test whether the loss of prepupal diapause is followed by genomic changes associated with lifespan extension, we compared 27 bee genomes with or without prepupal diapause. Our results point to several potential mechanisms for lifespan extension in species lacking prepupal diapause, including the loss of the growth hormone PTTH and its receptor TORSO, along with convergent selection in genes known to regulate lifespan in animals. Specifically, we observed purifying selection of prolongevity genes and relaxed selection of antilongevity genes within the IIS/TOR pathway in species that have lost prepupal diapause. Changes in selection pressures on this pathway may lead to the evolution of new phenotypes, such as lifespan extension and altered responses to nutritional signals that are crucial for social evolution.
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Research summary
The paper explores the evolutionary loss of developmental diapause in bees and its association with extended lifespan, which directly relates to mechanisms of lifespan extension. While the findings provide insights into genetic factors influencing longevity, the study is primarily focused on evolutionary biology rather than directly addressing the root causes of aging in a broader context. Thus, it represents solid research but with limited impact on the field of longevity research.
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