Wan Pin-Jun, Guo Wei-Yan, Yang Yao, Lü Feng-Gong, Lu Wei-Ping, Li Guo-Qing
Education Ministry Key Laboratory of Integrated Management of Crop Diseases and Pests, College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, China.
J Insect Physiol. 2014 Apr;63:48-55. doi: 10.1016/j.jinsphys.2014.02.009. Epub 2014 Mar 4.
Leptinotarsadecemlineata is the most important pest in potato and causes serious yield loss each year. Chlorantraniliprole acts on insect ryanodine receptors (RyRs) and is among the most active compounds against L. decemlineata. Here we cloned and characterized a 15,792-bp full-length LdRyR cDNA that encoded a 5128-amino acid protein. LdRyR shares 85-92% amino acid similarities with other insect RyR homologues, and 59-61% similarities with those from Caenorhabditis elegans and Homo sapiens. All hallmarks of the RyR proteins are conserved in LdRyR. LdRyR has a MIR domain, two RIH domains, three SPRY domains, four copies of RyR domain and a RIH-associated domain in the N-terminus, and it possesses two consensus calcium ion-binding EF-hand motifs and six predicted transmembrane helices in the C-terminus. Temporal, spatial and tissue-specific expression patterns of LdRyR were evaluated. LdRyR expression level was increased constantly from egg to wandering stages, dropped in pupal stage and was increased again in the adult stage. It was widely expressed in the head, thorax and abdomen of day 3 fourth-instar larvae. Moreover, it was ubiquitously expressed in all inspected tissues including epidermis, foregut, midgut, ileum, rectum, fat body, ventral ganglia and Malpighian tubules in day 3 fourth-instar larvae. Dietary introduction of double-stranded RNA of LdRyR significantly reduced the mRNA levels of the target gene in the larvae and adults, respectively, and significantly decreased chlorantraniliprole-induced mortalities. Thus, our results suggested that LdRyR encoded a functional ryanodine receptor in L. decemlineata.
马铃薯甲虫是马铃薯最重要的害虫,每年都会导致严重的产量损失。氯虫苯甲酰胺作用于昆虫的兰尼碱受体(RyRs),是对马铃薯甲虫活性最高的化合物之一。在此,我们克隆并鉴定了一个15792bp的全长LdRyR cDNA,其编码一个5128个氨基酸的蛋白质。LdRyR与其他昆虫RyR同源物的氨基酸相似度为85%-92%,与秀丽隐杆线虫和人类的相似度为59%-61%。RyR蛋白的所有特征在LdRyR中均保守。LdRyR在N端有一个MIR结构域、两个RIH结构域、三个SPRY结构域、四个RyR结构域拷贝和一个RIH相关结构域,在C端有两个保守的钙离子结合EF-手基序和六个预测的跨膜螺旋。评估了LdRyR的时空及组织特异性表达模式。LdRyR的表达水平从卵期到幼虫游走期持续升高,在蛹期下降,在成虫期再次升高。在3日龄四龄幼虫的头部、胸部和腹部广泛表达。此外,在3日龄四龄幼虫的所有检测组织中均有普遍表达,包括表皮、前肠、中肠、回肠、直肠、脂肪体、腹神经节和马氏管。通过饲料引入LdRyR的双链RNA分别显著降低了幼虫和成虫中靶基因的mRNA水平,并显著降低了氯虫苯甲酰胺诱导的死亡率。因此,我们的结果表明LdRyR在马铃薯甲虫中编码一种功能性的兰尼碱受体。