School of Life Sciences, Jiangsu University, Zhenjiang, China.
Jiangsu Key Laboratory for Biodiversity and Biotechnology, College of Life Sciences, Nanjing Normal University, Nanjing, China.
Pest Manag Sci. 2024 Aug;80(8):3734-3742. doi: 10.1002/ps.8076. Epub 2024 Mar 22.
Actin-related protein 2/3 complex regulates actin polymerization and the formation of branched actin networks. However, the function and evolutionary relationship of this complex subunit 2 (Arpc2) has been poorly understood in insects.
To address these issues, we performed comprehensive analysis of Arpc2 in Tribolium castaneum. Phylogenetic analysis revealed that Arpc2 was originated from one ancestral gene in animals but evolved independently between vertebrates and insects after species differentiation. T. castaneum Arpc2 has a 906-bp coding sequence and consists of 4 exons. Arpc2 transcripts were abundantly detected in embryos and pupae but less so in larvae and adults, while it had high expression in the gut, fat body and head but low expression in the epidermis of late-stage larvae. Knockdown of it at the late larval stage inhibited the pupation and resulted in arrested larvae. Silencing it in 1-day pupae impaired eclosion, which caused adult wings to fail to close. Injection of Arpc2 dsRNAs into 5-day pupae made adults have smaller testis and ovary and could not lay eggs. The expression of vitellogenin 1 (Vg1), Vg2 and Vg receptor (VgR) was downregulated after knocking down Arpc2 5 days post-adult emergence. Arpc2 silencing reduced 20-hydroxyecdysone titer by affecting the enzymes of its biosynthesis and catabolism but increased juvenile biosynthesis via upregulating JHAMT3 expression.
Our results indicate that Arpc2 is associated with the metamorphosis and reproduction by integrating ecdysone and juvenile hormone metabolism in T. castaneum. This study provides theoretical basis for developing Arpc2 as a potential RNA interference target for pest control. © 2024 Society of Chemical Industry.
肌动蛋白相关蛋白 2/3 复合物调节肌动蛋白聚合和分支肌动蛋白网络的形成。然而,该复合物亚基 2(Arpc2)在昆虫中的功能和进化关系还知之甚少。
为了解决这些问题,我们对赤拟谷盗(Tribolium castaneum)中的 Arpc2 进行了全面分析。系统发育分析显示,Arpc2 起源于动物的一个祖先基因,但在物种分化后,脊椎动物和昆虫之间独立进化。T. castaneum Arpc2 有一个 906bp 的编码序列,由 4 个外显子组成。Arpc2 转录本在胚胎和蛹中大量检测到,但在幼虫和成虫中较少,而在肠道、脂肪体和头部中高表达,在晚期幼虫的表皮中低表达。在晚期幼虫期敲低其表达会抑制化蛹并导致幼虫停滞。在 1 日龄蛹期沉默它会损害蜕皮,导致成虫翅膀无法合拢。向 5 日龄蛹注射 Arpc2 dsRNAs 会使成虫的睾丸和卵巢变小,无法产卵。敲低 Arpc2 5 天后,卵黄蛋白原 1(Vg1)、Vg2 和 Vg 受体(VgR)的表达下调。Arpc2 沉默通过影响其生物合成和分解代谢的酶来降低 20-羟基蜕皮酮的浓度,但通过上调 JHAMT3 表达来增加幼虫生物合成。
我们的结果表明,Arpc2 通过整合蜕皮激素和保幼激素代谢参与赤拟谷盗的变态和繁殖。这项研究为将 Arpc2 作为害虫防治的潜在 RNA 干扰靶标提供了理论依据。© 2024 化学工业协会。