National Bureau of Animal Genetic Resources, Karnal, India.
Int J Immunogenet. 2014 Feb;41(1):81-9. doi: 10.1111/iji.12075. Epub 2013 Jul 6.
TLR8 mediates antiviral immunity by recognizing ssRNA viruses and triggers potent antiviral and antitumor immune responses. In this study, approximately 3.5 Kb nucleotide sequence data of caprine TLR8 gene were generated from one sample each of twelve different Indian goat breeds belonging to different geographical regions. Cloning and characterization of cDNA synthesized from RNA purified from goat spleen revealed TLR8 ORF to be of 3102 nucleotides long coding for 1033 amino acids similar to other ruminant species, that is sheep, buffalo and cattle. The sequence analysis at nucleotide level revealed goat TLR8 to be closer to buffalo sharing 99.6% homology, followed by cattle and sheep. Simple Modular Architecture Research Tool (SMART) used for the structural analysis of goat TLR8 showed the presence of 16 leucine-rich repeats (LRRs) along with single Toll/interleukin-1 receptor (TIR) domain. TIR domain when compared with other livestock species was found to be conserved in ruminant species goat, sheep, cattle and buffalo. The phylogenetic analysis also revealed grouping of all ruminant species together, goat being closer to buffalo followed by cattle and sheep. Total 4 polymorphic sites were observed in TLR8 gene of one specimen goat representing each of 12 different breeds studied, all of which were synonymous and present within the coding region. Of these 4 SNPs, two were in ectodomains, one in TIR domain and one was found to be present in transmembrane domain. PCR-RFLP genotyping of two of the SNPs indicated variations in allele frequencies among different goat breeds. The expression profiling in 13 tissues of goat showed maximum expression of TLR8 gene in kidney followed by spleen, lung and lymph node. Overall, our results indicate conservation of TLR8 gene among the ruminant species and low variation within Indian goat breeds.
TLR8 通过识别 ssRNA 病毒来介导抗病毒免疫,并引发强烈的抗病毒和抗肿瘤免疫反应。在这项研究中,从来自不同地理区域的 12 个不同印度山羊品种的每个品种中获得了约 3.5kb 的核苷酸序列数据。从从山羊脾脏中提取的 RNA 合成的 cDNA 的克隆和表征揭示了 TLR8 ORF 长 3102 个核苷酸,编码 1033 个与其他反刍动物物种(即绵羊、水牛和牛)相似的氨基酸。核苷酸水平的序列分析表明,山羊 TLR8 与水牛更为接近,同源性为 99.6%,其次是牛和绵羊。用于分析山羊 TLR8 结构的简单模块化架构研究工具 (SMART) 显示存在 16 个富含亮氨酸的重复序列 (LRRs) 以及单个 Toll/白细胞介素-1 受体 (TIR) 结构域。与其他牲畜物种相比,TIR 结构域在反刍动物物种(山羊、绵羊、牛和水牛)中被保守。系统发育分析还表明,所有反刍动物物种都聚集在一起,山羊与水牛关系更密切,其次是牛和绵羊。在所研究的 12 个不同品种的每一个山羊样本中,共观察到 TLR8 基因中的 4 个多态性位点,这些多态性均为同义突变,且位于编码区。这 4 个 SNP 中,有 2 个位于外显子,1 个位于 TIR 结构域,1 个位于跨膜结构域。对其中 2 个 SNP 的 PCR-RFLP 基因分型表明,不同山羊品种之间等位基因频率存在差异。在 13 种组织中的表达谱显示,TLR8 基因在肾脏中的表达最高,其次是脾脏、肺和淋巴结。总的来说,我们的研究结果表明 TLR8 基因在反刍动物物种中是保守的,而在印度山羊品种中则是低变的。