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利用转录组分析鉴定丽蝇蛹集金小蜂(膜翅目:姬蜂科)中的谷胱甘肽-S-转移酶基因及其在辛硫磷和氯氰菊酯胁迫下的表达模式。

Identification of glutathione-S-transferase genes by transcriptome analysis in Meteorus pulchricornis (Hymenoptera: Braconidae) and their expression patterns under stress of phoxim and cypermethrin.

机构信息

School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang 212018, PR China.

School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang 212018, PR China; School of Hanlin, Nanjing University of China Medicine, Taizhou 225300, PR China.

出版信息

Comp Biochem Physiol Part D Genomics Proteomics. 2019 Sep;31:100607. doi: 10.1016/j.cbd.2019.100607. Epub 2019 Jul 9.

Abstract

Meteorus pulchricornis (Wesmael) (Hymenoptera: Braconidae) is a preponderant endoparasitoid wasp, attacking the larvae of many lepidopteran pests. We present the first body transcriptome dataset for M. pulchricornis. In total, 50,781,796 clean reads were obtained and 33,144 unigenes were assembled; 15,458 unigenes showed a significant similarity (E value < 10) to known proteins in the NCBI non-redundant protein database. Gene ontology and cluster of orthologous group analyses were performed to classify the functions of genes. To better understand the role of glutathione-S-transferases (GSTs) in detoxification mechanism in M. pulchricornis, we identified seventeen GST genes (MpulGSTs) from the body transcriptome. Among these, fifteen MpulGSTs belonged to cytosolic GSTs and the other two belonged to microsomal classes. The cytosolic GSTs were classified into four different clades: four in delta, three in omega, seven in sigma, and one in zeta. The expression levels of these MpulGSTs after exposure to sub-lethal concentrations of phoxim and cypermethrin were determined using real-time quantitative polymerase chain reaction: seven MpulGSTs (MpulGSTD3, MpulGSTS1, MpulGSTS2, MpulGSTS4, MpulGSTS6 MpulGSTO3, and MpulGSTmic1) and 11 MpulGSTs (MpulGSTD1, MpulGSTD2, MpulGSTD3, MpulGSTO2, MpulGSTS1, MpulGSTS2, MpulGSTS3, MpulGSTS4, MpulGSTS5, MpulGSTS7, and MpulGSTmic1) were highly expressed, respectively. These results suggested that GST genes may play a pivotal role in detoxification process in M. pulchricornis. Our findings would provide a theoretical base for elucidating insecticide susceptibility and should promote functional research on specific GST genes in parasitoid wasps.

摘要

丽蝇蛹集金小蜂(Meteorus pulchricornis)(膜翅目:Braconidae)是一种优势的内寄生蜂,攻击许多鳞翅目害虫的幼虫。我们呈现了第一个丽蝇蛹集金小蜂的身体转录组数据集。总共获得了 50781796 条清洁读数,组装了 33144 个非冗余基因;15458 个非冗余基因与 NCBI 非冗余蛋白质数据库中的已知蛋白质具有显著相似性(E 值<10)。进行了基因本体和直系同源群分析,以分类基因的功能。为了更好地了解谷胱甘肽-S-转移酶(GSTs)在丽蝇蛹集金小蜂解毒机制中的作用,我们从身体转录组中鉴定了十七个 GST 基因(MpulGSTs)。其中,十五个 MpulGSTs 属于细胞溶质 GSTs,另外两个属于微粒体类。细胞溶质 GSTs 分为四个不同的分支:四个属于 delta,三个属于 omega,七个属于 sigma,一个属于 zeta。使用实时定量聚合酶链反应测定了这些 MpulGSTs 在暴露于亚致死浓度的辛硫磷和氯氰菊酯后的表达水平:七个 MpulGSTs(MpulGSTD3、MpulGSTS1、MpulGSTS2、MpulGSTS4、MpulGSTS6、MpulGSTO3 和 MpulGSTmic1)和 11 个 MpulGSTs(MpulGSTD1、MpulGSTD2、MpulGSTD3、MpulGSTO2、MpulGSTS1、MpulGSTS2、MpulGSTS3、MpulGSTS4、MpulGSTS5、MpulGSTS7 和 MpulGSTmic1)分别高度表达。这些结果表明 GST 基因可能在丽蝇蛹集金小蜂的解毒过程中发挥关键作用。我们的发现将为阐明昆虫对杀虫剂的敏感性提供理论基础,并应促进寄生蜂中特定 GST 基因的功能研究。

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