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利用跨物种微阵列杂交技术对斯氏按蚊抗杀虫剂能力进行转录分析。

Transcriptional analysis of insecticide resistance in Anopheles stephensi using cross-species microarray hybridization.

作者信息

Vontas J, David J-P, Nikou D, Hemingway J, Christophides G K, Louis C, Ranson H

机构信息

Laboratory of Pesticide Science, Agricultural University of Athens, Athens, Greece.

出版信息

Insect Mol Biol. 2007 Jun;16(3):315-24. doi: 10.1111/j.1365-2583.2007.00728.x. Epub 2007 Apr 13.

Abstract

A large scale microarray (20k MMC1) from the African malaria vector Anopheles gambiae was used to monitor gene expression in insecticide resistant and susceptible strains of the Asian mosquito Anopheles stephensi. Heterologous hybridization at slightly reduced stringency yielded approximately 7000 significant signals. Thirty-six putative genes were differentially transcribed between the pyrethroid-resistant (DUB-R) and the susceptible (BEECH) strains. The expression profiles of selected transcripts were verified by real-time PCR. A gene putatively involved in the thickening of the adult cuticle showed the most striking up-regulation in DUB-R. A more specialized microarray containing 231 An. gambiae genes putatively involved in insecticide detoxification was used to further analyse classical insecticide resistance genes. Three glutathione S-transferase (GST) transcripts, one esterase and a cytochrome P450 were up-regulated in the resistant strain, while two peroxidases were down-regulated.

摘要

利用来自非洲疟疾媒介冈比亚按蚊的大规模微阵列(20k MMC1)监测亚洲蚊虫斯氏按蚊抗杀虫剂品系和敏感品系中的基因表达。在略微降低严谨度的条件下进行异源杂交产生了约7000个显著信号。在拟除虫菊酯抗性品系(DUB-R)和敏感品系(BEECH)之间有36个推定基因的转录存在差异。通过实时PCR验证了所选转录本的表达谱。一个推定参与成虫表皮增厚的基因在DUB-R中表现出最显著的上调。使用一个包含231个推定参与杀虫剂解毒的冈比亚按蚊基因的更专门化微阵列,进一步分析经典的抗杀虫剂基因。抗性品系中有3个谷胱甘肽S-转移酶(GST)转录本、1个酯酶和1个细胞色素P450上调,而2个过氧化物酶下调。

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