叶尔羌野兔和美洲野兔肠道 TLR4 基因表达和功能验证的比较分析

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Liukai Zhang, Dingwei Shao, Junyao You, Penggang Liu, Fang Deng, Jianping Zhang
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引用次数: 0

摘要

叶尔羌鹅常年生活在恶劣的沙漠环境中,对肠炎的易感性较低。TLR4与肠炎的发生密切相关,基于12S rDNA序列的邻接拓扑显示,乌头野兔与叶尔羌野兔之间的关系高达98%。本研究的目的是探讨 Toll 样受体 4(Toll-like receptor 4,TLR4)在调节大肠杆菌肠道免疫和炎症中的作用。本研究首次克隆了亚克兰氏梭子蟹结肠中的 TLR4 基因。通过组织学观察、实时荧光定量PCR(qRT-PCR)和蛋白印迹(Western blot)检测了TLR4在L.yarkandensis和O.cuniculus肠道组织中的表达。结果表明,L. yarkandensis TLR4基因的开放阅读框长度为2520 bp。与O. cuniculus的序列相比,L. yarkandensis的TLR4氨基酸序列有15处差异,其中12处发生在LRR结构域,2处发生在TIR结构域,序列在298位由G变为D。免疫组化结果表明,TLR4主要表达于L. yarkandensis结肠的上皮细胞,与O. cuniculus相比,TLR4在盲肠和结肠中的表达水平明显降低;qRT-PCR和Western blot结果表明,TLR4在L. yarkandensis结肠中的表达水平明显低于O. cuniculus。在细胞水平上,酶联免疫吸附试验(ELISA)表明,过量表达 TLR4 蛋白可降低 LPS 诱导的炎症反应。因此,根据上述结果,叶尔羌蛙TLR4的蛋白结构和功能可能因核苷酸的改变而不同,从而影响其与LPS的结合及下游分子的活化,使叶尔羌蛙不易发生肠炎,并能长期适应恶劣的沙漠环境。这项研究也为提高O. cuniculus的抗病能力和促进L. Yarkandensis基因的开发利用奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Analysis of Intestinal TLR4 Gene Expression and Functional Verification in Lepus yarkandensis and Oryctolagus cuniculus.

Lepus yarkandensis live year-round in harsh desert environments and are less susceptible to enteritis. The living conditions of Oryctolagus cuniculus in captivity were suitable, but they were highly susceptible to death by Gram-negative bacteria infected with inflammatory bowel disease complex.TLR4 is closely related to the occurrence of enteritis, and the neighbor-joining topology based on the 12S rDNA sequences showed that the relationship between O. cuniculus and L. yarkandensis is as high as 98%.Therefore, we chose O. cuniculus and L. yarkandensis for comparative study.The purpose of this study was to investigate the role of Toll-like receptor 4 (TLR4) in the regulation of immunity and inflammation in the intestinal tract of L. yarkandensis. In this study, the TLR4 gene was cloned for the first time in the colon of L. yarkandensis. The expression of TLR4 in the intestinal tissues of L. yarkandensis and O. cuniculus was detected by histological observation, real-time fluorescence quantification PCR(qRT-PCR), and protein blotting (Western blot).An LPS-induced cell inflammation model was constructed in vitro, and ELISA was used to examine the effect of pEGFP-N1-TLR4 and siRNA knockout on the anti-inflammatory ability of the TLR4 gene. The results showed that the open reading frame of the L. yarkandensis TLR4 gene was 2520 bp in length. Compared with the sequence of O. cuniculus, there were 15 differences in the TLR4 amino acid sequence of L. yarkandensis, 12 of which occurred in the LRR domain and 2 in the TIR domain, and the sequence changed from G to D at position 298. Immunohistochemistry showed that TLR4 was mainly expressed in the epithelial cells of the colon L. yarkandensis, and the expression level of TLR4 in the cecum and colon was significantly lower compared with that of O. cuniculus. qRT-PCR and Western blot results showed that the expression level of TLR4 in the colon of L. yarkandensis was significantly lower than that of O. cuniculus. At the cellular level, ELISA showed that overexpression of the TLR4 protein in L. yarkandensis could reduce the LPS-induced inflammatory response. Therefore, according to the above results, the protein structure and function of L. yarkandensis TLR4 may be different due to the change of nucleotide, which affects its binding with LPS and the activation of downstream molecules, so that L. yarkandensis is not prone to enteritis and can adapt to the harsh desert environment for a long time. This study also laid the foundation for improving the disease resistance of O. cuniculus and promoting the development and utilization of genes in L. yarkandensis.

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来源期刊
Biochemical Genetics
Biochemical Genetics 生物-生化与分子生物学
CiteScore
3.90
自引率
0.00%
发文量
133
审稿时长
4.8 months
期刊介绍: Biochemical Genetics welcomes original manuscripts that address and test clear scientific hypotheses, are directed to a broad scientific audience, and clearly contribute to the advancement of the field through the use of sound sampling or experimental design, reliable analytical methodologies and robust statistical analyses. Although studies focusing on particular regions and target organisms are welcome, it is not the journal’s goal to publish essentially descriptive studies that provide results with narrow applicability, or are based on very small samples or pseudoreplication. Rather, Biochemical Genetics welcomes review articles that go beyond summarizing previous publications and create added value through the systematic analysis and critique of the current state of knowledge or by conducting meta-analyses. Methodological articles are also within the scope of Biological Genetics, particularly when new laboratory techniques or computational approaches are fully described and thoroughly compared with the existing benchmark methods. Biochemical Genetics welcomes articles on the following topics: Genomics; Proteomics; Population genetics; Phylogenetics; Metagenomics; Microbial genetics; Genetics and evolution of wild and cultivated plants; Animal genetics and evolution; Human genetics and evolution; Genetic disorders; Genetic markers of diseases; Gene technology and therapy; Experimental and analytical methods; Statistical and computational methods.
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