Wertheim Bregje, Kraaijeveld Alex R, Schuster Eugene, Blanc Eric, Hopkins Meirion, Pletcher Scott D, Strand Michael R, Partridge Linda, Godfray H Charles J
Centre for Evolutionary Genomics, Department of Biology, University College London, London WC1E 6BT, UK.
Genome Biol. 2005;6(11):R94. doi: 10.1186/gb-2005-6-11-r94. Epub 2005 Oct 31.
Parasitoids are insect parasites whose larvae develop in the bodies of other insects. The main immune defense against parasitoids is encapsulation of the foreign body by blood cells, which subsequently often melanize. The capsule sequesters and kills the parasite. The molecular processes involved are still poorly understood, especially compared with insect humoral immunity.
We explored the transcriptional response to parasitoid attack in Drosophila larvae at nine time points following parasitism, hybridizing five biologic replicates per time point to whole-genome microarrays for both parasitized and control larvae. We found significantly different expression profiles for 159 probe sets (representing genes), and we classified them into 16 clusters based on patterns of co-expression. A series of functional annotations were nonrandomly associated with different clusters, including several involving immunity and related functions. We also identified nonrandom associations of transcription factor binding sites for three main regulators of innate immune responses (GATA/srp-like, NF-kappaB/Rel-like and Stat), as well as a novel putative binding site for an unknown transcription factor. The appearance or absence of candidate genes previously associated with insect immunity in our differentially expressed gene set was surveyed.
Most genes that exhibited altered expression following parasitoid attack differed from those induced during antimicrobial immune responses, and had not previously been associated with defense. Applying bioinformatic techniques contributed toward a description of the encapsulation response as an integrated system, identifying putative regulators of co-expressed and functionally related genes. Genome-wide studies such as ours are a powerful first approach to investigating novel genes involved in invertebrate immunity.
寄生蜂是昆虫寄生虫,其幼虫在其他昆虫体内发育。针对寄生蜂的主要免疫防御是血细胞对异物进行包囊化,随后异物通常会黑化。包囊会隔离并杀死寄生虫。所涉及的分子过程仍知之甚少,尤其是与昆虫体液免疫相比。
我们在寄生后的九个时间点探究了果蝇幼虫对寄生蜂攻击的转录反应,每个时间点将五个生物学重复样本与寄生和对照幼虫的全基因组微阵列进行杂交。我们发现159个探针集(代表基因)的表达谱存在显著差异,并根据共表达模式将它们分为16个簇。一系列功能注释与不同簇非随机相关,包括一些涉及免疫和相关功能的注释。我们还确定了先天免疫反应的三个主要调节因子(GATA/srp样、NF-κB/Rel样和Stat)的转录因子结合位点的非随机关联,以及一个未知转录因子的新推定结合位点。我们调查了差异表达基因集中先前与昆虫免疫相关的候选基因的出现或缺失情况。
大多数在寄生蜂攻击后表达发生改变的基因与抗菌免疫反应期间诱导的基因不同,并且以前未与防御相关联。应用生物信息学技术有助于将包囊化反应描述为一个整合系统,识别共表达和功能相关基因的推定调节因子。像我们这样的全基因组研究是研究参与无脊椎动物免疫的新基因的有力的第一步方法。