Plant Protection Department, Economic Entomology Research Unit, College of Food and Agriculture Sciences, King Saud University, Riyadh, Saudi Arabia.
Ghazi University, Dera Ghazi Khan, Punjab, Pakistan.
PLoS One. 2021 Feb 11;16(2):e0245928. doi: 10.1371/journal.pone.0245928. eCollection 2021.
Vitellogenins, major yolk protein precursors, play an essential role in the reproduction and spread of all oviparous species, including insects. To investigate reproductive strategies of the warehouse moth Cadra cautella at the molecular level, a partial transcript of the C. cautella vitellogenin (CcVg) gene was extended through the rapid amplification of cDNA ends PCR and sequenced. The complete CcVg mRNA transcript was 5,334 bp long, which encoded a protein of 1,778 amino acids, including the first 14 amino acids of the signal peptide. The deduced CcVg protein contained a putative cleavage site (RTRR) at the amino-terminal side, similar to several other insect species. DGQR and GI/LCG motifs were present at the CcVg gene C-terminus, followed by nine cysteine residues. CcVg harbored 131 putative phosphorylation sites, numbering 84, 19, and 28 sites for serine, threonine, and tyrosine, respectively. The transcript showed a great resemblance with other lepidopteran Vgs. CcVg protein analysis revealed three conserved regions: 1) vitellogenin-N domain, 2) DUF 1943 (domain of unknown function), and 3) a von Willebrand factor type D domain. Additionally, sex, stage-specific, and developmental expression profiles of the CcVg gene were determined through RT-PCR. The Vg was first expressed in 22-day-old female larvae, and its expression increased with growth. The phylogenetic analysis based on different insect Vgs revealed that the CcVg exhibited close ancestry with lepidopterans. The CcVg-based RNAi experiments were performed, and the effects were critically evaluated. The qRT-PCR results showed that CcVg-based dsRNA suppressed the Vg gene expression up to 90% at 48 h post-injection. Moreover, CcVg-based RNAi effects resulted in low fecundity and egg hatchability in the CcVg-based dsRNA-treated females. The females laid eggs, but because of insufficient yolk protein availability the eggs could not succeed to hatch. The significant difference in the fecundity and hatchability unveils the importance of CcVg gene silencing and confirmed that the Vg gene plays a key role in C. cautella reproduction and it has the potential to be used as a target for RNAi-mediated control of this warehouse pest.
卵黄蛋白原是卵黄蛋白前体的主要成分,在所有卵生动物(包括昆虫)的繁殖和传播中起着至关重要的作用。为了从分子水平上研究仓库 moth Cadra cautella 的繁殖策略,通过快速扩增 cDNA 末端 PCR 延伸了 C. cautella 卵黄蛋白原(CcVg)基因的部分转录本,并对其进行了测序。完整的 CcVg mRNA 转录本长 5334bp,编码 1778 个氨基酸的蛋白质,包括信号肽的前 14 个氨基酸。推导的 CcVg 蛋白在氨基末端有一个假定的切割位点(RTRR),类似于其他几种昆虫。CcVg 基因 C 末端存在 DGQR 和 GI/LCG 基序,后面跟着 9 个半胱氨酸残基。CcVg 含有 131 个假定的磷酸化位点,分别为丝氨酸 84 个、苏氨酸 19 个和酪氨酸 28 个。该转录本与其他鳞翅目 Vgs 非常相似。CcVg 蛋白分析揭示了三个保守区域:1)卵黄蛋白原-N 结构域,2)DUF 1943(未知功能结构域),3)von Willebrand 因子 D 型结构域。此外,通过 RT-PCR 确定了 CcVg 基因的性别、阶段特异性和发育表达谱。Vg 首先在 22 天大的雌性幼虫中表达,并随生长而增加。基于不同昆虫 Vgs 的系统发育分析表明,CcVg 与鳞翅目昆虫具有密切的亲缘关系。进行了基于 CcVg 的 RNAi 实验,并对其效果进行了严格评估。qRT-PCR 结果表明,注射后 48 小时,基于 CcVg 的 dsRNA 可将 Vg 基因表达抑制高达 90%。此外,基于 CcVg 的 RNAi 作用导致基于 CcVg 的 dsRNA 处理的雌性产卵量和卵孵化率降低。雌性产卵,但由于卵黄蛋白供应不足,卵无法成功孵化。在繁殖力和孵化率方面的显著差异揭示了 CcVg 基因沉默的重要性,并证实 Vg 基因在 C. cautella 的繁殖中起着关键作用,它有可能被用作这种仓库害虫的 RNAi 介导控制的靶标。