Chen Ming-Shun, Zhao Hui-Xian, Zhu Yu Cheng, Scheffler Brian, Liu Xuming, Liu Xiang, Hulbert Scot, Stuart Jeffrey J
USDA-ARS Plant Science and Entomology Research Unit, 4008 Throckmorton Hall, 1515 College Avenue, Manhattan, KS 66506, USA.
J Insect Physiol. 2008 Jan;54(1):1-16. doi: 10.1016/j.jinsphys.2007.07.007. Epub 2007 Aug 10.
Hessian fly (Mayetiola destructor) larvae are thought to manipulate host growth and metabolism through salivary secretions. However, the transcriptome and proteome of Hessian fly salivary glands have not been systematically analyzed. In this research, we analyzed Expressed-Sequence-Tags (EST) representing 6106 cDNA clones randomly selected from four libraries made from dissected salivary glands. We also analyzed the protein composition of dissected salivary glands using one- and two-dimensional gel electrophoresis as well as LC-MS/MS analysis. Transcriptomic analysis revealed that approximately 60% of the total cDNA clones and 40% of assembled clusters encoded secretory proteins (SP). The SP-encoding cDNAs were grouped into superfamilies and families according to sequence similarities. In addition to the high percentage of SP-encoding transcripts, there was also a high percentage of transcripts encoding proteins that were either involved directly in protein synthesis or in house-keeping functions that provide conditions necessary for protein synthesis. Proteomic analysis also revealed a high percentage of proteins involved in protein synthesis either directly or indirectly. The high percentage of SP-encoding transcripts and high percentage of proteins related to protein synthesis suggested that the salivary glands of Hessian fly larvae are indeed specialized tissues for synthesis of proteins for host injection. However, LC-MS/MS analysis of 64 proteins did not identify any SPs corresponding to the cDNA sequences. The lack of accumulation of SPs in the salivary glands indicated the SPs were likely secreted as soon as they were synthesized.
小麦瘿蚊(Mayetiola destructor)幼虫被认为通过唾液分泌物来操控宿主的生长和新陈代谢。然而,尚未对小麦瘿蚊唾液腺的转录组和蛋白质组进行系统分析。在本研究中,我们分析了从解剖的唾液腺构建的四个文库中随机选取的6106个cDNA克隆所代表的表达序列标签(EST)。我们还使用一维和二维凝胶电泳以及液相色谱 - 串联质谱分析(LC - MS/MS分析)来分析解剖的唾液腺的蛋白质组成。转录组分析表明,总cDNA克隆的约60%以及组装簇的40%编码分泌蛋白(SP)。根据序列相似性,编码SP的cDNA被归类为超家族和家族。除了编码SP的转录本比例较高外,编码直接参与蛋白质合成或参与为蛋白质合成提供必要条件的管家功能的蛋白质的转录本比例也很高。蛋白质组分析还揭示了直接或间接参与蛋白质合成的蛋白质比例很高。编码SP的转录本比例高以及与蛋白质合成相关的蛋白质比例高表明,小麦瘿蚊幼虫的唾液腺确实是用于合成注入宿主的蛋白质的特化组织。然而,对64种蛋白质的LC - MS/MS分析未鉴定出任何与cDNA序列对应的SP。唾液腺中SP缺乏积累表明SP可能一旦合成就被分泌。