脊椎动物toll样受体病原体核酸特异性分析与预测

IF 4.7 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Biology Pub Date : 2023-09-01 DOI:10.1016/j.jmb.2023.168208
Anuja Jain, Tina Begum, Shandar Ahmad
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引用次数: 0

摘要

鉴定核酸敏感宿主蛋白的关键序列、表达和功能相关特征对了解病原体特异性宿主反应的动态具有重要意义。为了实现这一目标,我们在本比较研究中考虑了toll样受体(TLRs),这是一类具有代表性的膜结合传感器蛋白,来自17种脊椎动物物种,包括哺乳动物,鸟类,爬行动物,两栖动物和鱼类。我们确定了宿主tlr的分子特征,这些分子特征负责感知病原体核酸或其他病原体相关分子模式(PAMPs),并可能在宿主防御机制中发挥重要作用。有趣的是,我们的研究结果表明,这种宿主特异性特征与病原体核酸的链(单或双)特异性直接相关。然而,在宿主-病原体相互作用过程中,这些特征无法解释致病性PAMP(即DNA、RNA或其他)的选择性,提示其机制更为复杂。利用这些特征,我们开发了许多机器学习模型,其中Random Forest在从蛋白质衍生特征预测tlr链特异性方面取得了很高的性能(准确率为94.57%)。我们应用训练模型提出了一些以前未被表征的独特的鱼类特异性新tlr (TLR18, TLR23, TLR24, TLR25, TLR27)的链特异性。
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Analysis and Prediction of Pathogen Nucleic Acid Specificity for Toll-like Receptors in Vertebrates

Identification of key sequence, expression and function related features of nucleic acid-sensing host proteins is of fundamental importance to understand the dynamics of pathogen-specific host responses. To meet this objective, we considered toll-like receptors (TLRs), a representative class of membrane-bound sensor proteins, from 17 vertebrate species covering mammals, birds, reptiles, amphibians, and fishes in this comparative study. We identified the molecular signatures of host TLRs that are responsible for sensing pathogen nucleic acids or other pathogen-associated molecular patterns (PAMPs), and potentially play important roles in host defence mechanism. Interestingly, our findings reveal that such host-specific features are directly related to the strand (single or double) specificity of nucleic acid from pathogens. However, during host-pathogen interactions, such features were unable to explain the pathogenic PAMP (i.e., DNA, RNA or other) selectivity, suggesting a more complex mechanism. Using these features, we developed a number of machine learning models, of which Random Forest achieved a high performance (94.57% accuracy) to predict strand specificity of TLRs from protein-derived features. We applied the trained model to propose strand specificity of some previously uncharacterized distinct fish-specific novel TLRs (TLR18, TLR23, TLR24, TLR25, TLR27).

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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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