Differences in ASP1 expression and binding dynamics to queen mandibular pheromone HOB between Apis mellifera and Apis cerana workers reveal olfactory adaptation to colony organization.
Differences in ASP1 expression and binding dynamics to queen mandibular pheromone HOB between Apis mellifera and Apis cerana workers reveal olfactory adaptation to colony organization.
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DOI:
10.1016/j.ijbiomac.2022.07.064
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发表时间:
2022-07
影响因子:
8.2
通讯作者:
Fan Wu;Shenyun Liu;Xufeng Zhang;Han Hu;Qiaohong Wei;Bin Han;Hongliang Li
中科院分区:
文献类型:
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作者:
Fan Wu;Shenyun Liu;Xufeng Zhang;Han Hu;Qiaohong Wei;Bin Han;Hongliang Li
The easternApis cerana(Ac) and the westernApis mellifera(Am) are two closely related and most economically valuable honeybee species managed extensively worldwide. However, how worker bees ofAcandAmare adapted to their colony organization remains to be uncovered. Here, we found that the expression level of gene encoding antennae-specific proteins 1 (ASP1, a key regulator in recognizing queen mandibular pheromone) was positively correlated with the colony sizes in both bee species, and the expression level inAmwas higher than that inAc, suggesting that ASP1 may play an important role in maintaining colony homeostasis. Using competitive binding assay, molecular docking, and site-directed mutagenesis, we then confirmed the good binding affinities of both Ac-ASP1 and Am-ASP1 to methyl p-hydroxy benzoate (HOB), and Val115 was the key amino acid. However, the affinity of Am-ASP1 was stronger than that of Ac-ASP1. EAG analysis further demonstrated that antennae ofAmworker bees had faster depolarization and repolarization in response to HOB stimulation. Taken together, these findings indicate that the differences in expression levels and binding dynamics allow ASP1 recognizing HOB to potentially serve as a specific regulator of colony organization inAcandAm.