Franch Rafaella, Cardazzo Barbara, Antonello Jenny, Castagnaro Massimo, Patarnello Tomaso, Bargelloni Luca
Department of Public Health, Comparative Pathology, and Veterinary Hygiene, University of Padova, viale dell'Università 16, 35020 Legnaro (Pd), Italy.
Gene. 2006 Aug 15;378:42-51. doi: 10.1016/j.gene.2006.04.025. Epub 2006 May 11.
Toll-Like Receptors (TLRs) have recently emerged as key sensors of invading microbes, acting through recognition of pathogen-associated molecular patterns. It has been demonstrated that TLR9 is involved in the recognition of unmethylated CpG motifs in mice, humans, and pigs. We report here the full-length sequence of TLR9 cDNA in the gilthead sea bream (Sparus aurata L.). The predicted protein (1063 amino acids) was similar to mammalian TLR9s, showing 21 leucine-rich repeats in the extracellular region and a typical Toll/IL-1R (TIR) domain in the intracellular region. Comparative analysis of TLR9 sequences indicated that critical residues for ligand-binding are conserved across vertebrate lineages, although evidence of functional divergence was observed. Analysis of the genomic structure of sea bream TLR9 gene revealed the presence of two intervening sequences. Retention of the second intron produced an alternatively spliced mRNA (TLR9B) showing differential expression among tissues or developmental stages compared to the wild-type isoform (TLR9A). RT-PCR analysis indicated a broad expression of TLR9A, especially in immune-related organs (spleen, head-kidney) and mucosal-epithelial barriers (gills, gut, skin). Using quantitative Real-Time RT-PCR, no statistically significant variation was observed for TLR9 mRNAs expression in the spleen of experimentally infected animals compared to healthy controls. Comparing sequence and expression profile of sea bream TLR9 with mammalian TLR9s suggested that the main function of TLR9 might be conserved across vertebrates, although species-specific features are present (modulation of ligand-binding specificity, alternative splicing).
Toll样受体(TLRs)最近已成为入侵微生物的关键传感器,通过识别病原体相关分子模式发挥作用。已证明TLR9参与小鼠、人类和猪中未甲基化CpG基序的识别。我们在此报告金头鲷(Sparus aurata L.)中TLR9 cDNA的全长序列。预测的蛋白质(1063个氨基酸)与哺乳动物TLR9相似,在细胞外区域显示有21个富含亮氨酸的重复序列,在细胞内区域有一个典型的Toll/IL-1R(TIR)结构域。TLR9序列的比较分析表明,尽管观察到功能分化的证据,但配体结合的关键残基在脊椎动物谱系中是保守的。对金头鲷TLR9基因的基因组结构分析揭示了两个间隔序列的存在。第二个内含子的保留产生了一种可变剪接的mRNA(TLR9B),与野生型异构体(TLR9A)相比,其在组织或发育阶段之间表现出差异表达。RT-PCR分析表明TLR9A广泛表达,尤其是在免疫相关器官(脾脏、头肾)和粘膜上皮屏障(鳃、肠道、皮肤)中。使用定量实时RT-PCR,与健康对照相比,在实验感染动物的脾脏中未观察到TLR9 mRNA表达的统计学显著变化。将金头鲷TLR9的序列和表达谱与哺乳动物TLR9进行比较表明,尽管存在物种特异性特征(配体结合特异性的调节、可变剪接),但TLR9的主要功能可能在脊椎动物中是保守的。