天然免疫相关分子的进化
文献类型:学位论文
作者 | 李岩 |
学位类别 | 博士 |
答辩日期 | 2008-01 |
授予单位 | 中国科学院研究生院 |
授予地点 | 北京 |
导师 | 王文 |
关键词 | 天然免疫 肽聚糖识别受体SD 识别策略 抗菌肽 平衡选择 |
其他题名 | Evolution of innate immunity-related genes |
学位专业 | 动物学 |
中文摘要 | 本论文结合功能研究和进化遗传学方法对动物天然免疫(innate immunity)相关分子的进化历程进行深入研究。受体对病原微生物的识别是天然免疫系统发挥功能的基础。作为模式识别受体(pattern recognition receptor, PRR),果蝇肽聚糖识别蛋白SD(PGRP-SD)在识别革兰氏阳性细菌的过程中发挥了重要作用。针对已有的黑腹果蝇(Drosophila melanogaster)群体数据,我们发现PGRP-SD在群体中存在2类高频的等位基因(分别为等位基因1和等位基因2)。以D. simulans为外群,我们追溯了黑腹果蝇2类等位基因上氨基酸的变化。这些氨基酸的结构特征和在蛋白质上所处的位置提示这2类等位基因在功能方面可能存在分化。通过功能研究的方法,我们发现在黑腹果蝇中该基因功能方面发生了显著的变化。等位基因2在有微生物时能激活天然免疫反应,但等位基因1的转基因果蝇成虫只要有外伤即便没有微生物的情况下即能激发天然免疫反应,而带有等位基因2果蝇成虫则不具有该功能。这一结果提示我们,发生在该等位基因上的氨基酸变化导致了其识别功能的变化。与推导的祖先基因相比,等位基因1发生了一个氨基酸的变化,因此导致其功能从识别细菌细胞壁组分肽聚糖转变为一未知的自身组分,即从病原相关分子模式(pathogen-associated molecular pattern,PAMP)识别受体转变为损伤相关识别模式(damage-associated molecular pattern, DAMP)识别受体。通过这一功能变化, 果蝇成虫可以通过仅识别自身损伤即可激活相应的免疫反应,对后续可能侵入的微生物进行杀伤。已有研究结果显示,微生物在进化过程中已经形成针对DAMP和PAMP规避策略。上述2类等位基因的同时存在能使黑腹果蝇同时具备两个机制,更加充分地抵抗病原微生物的入侵。结合功能研究和针对自然群体的群体遗传学分析,我们认为在黑腹果蝇群体中以高频共存的2类PGRP-SD等位基因可能可能受到了平衡选择(balancing selection)作用。上述工作主要研究了天然免疫系统识别受体的进化。而本论文的另一部分则主要针对天然免疫系统的效应分子(effector)进行了研究。作为重要的效应分子,抗菌肽在杀菌方面发挥着最为直接的作用。因此,研究抗菌肽的进化对于探索天然免疫系统的进化具有重要意义。本研究以两栖类动物大蹼铃蟾抗菌肽基因家族为例,通过对分别来自2个大蹼铃蟾个体的皮肤cDNA文库进行测序,我们鉴别出56个不同的抗菌肽cDNA序列。每一个cDNA均编码2个不同的抗菌肽,maximin 和maximin H。基于针对这些cDNA序列的分析,我们发现2类抗菌肽编码序列的非同义替代率均高于同义替代率,呈现高度分化的特征。但是,在信号肽和其它非抗菌肽编码区域并没有发现这种情况。这一结果提示抗菌肽可能受到超显性选择(overdominent selection, 即平衡选择)的影响。同时,我们分别从皮肤和肝脏克隆基因了7个抗菌肽的基因组编码序列并进行了测序。这些从不同组织获得的抗菌肽在各个编码序列中均存在序列的差异的同时呈现了相同的结构。这一结果提示不同抗菌肽间的差异不太可能来自于体细胞突变而是快速序列进化的结果。通过构建来自于同一个体的抗菌肽的不同编码区的基因树,我们发现结构域重排(domain shuffling)和/或基因转换(gene conversion)在这些抗菌肽的进化历程中发挥作用。 |
英文摘要 | The recognition of pathogens by host receptors is a fundamental process of immunity. The peptidoglycan recognition protein SD (PGRP-SD), a pattern recognition receptor (PRR) of Drosophila innate immune system plays an important role in detecting Gram-positive bacteria. Here we used functional assay to explore the evolutionary and immune significance of changes appearing in the Drosophila melanogaster PGRP-SD gene. The results of clean injury on the transgenic lines’ adults indicated that the target of one major PGRP-SD allele has surprisingly shifted target from bacterial peptidoglycan (PGN) to self abnormally exposed connatural molecule in adults. One amino acid mutation on the allele 1 achieved a functional turnover from recognition of pathogen-accociated molecular pattern (PAMP) to that of damage-associated molecular pattern (DAMP). By checking the exposure of self molecule, the allele 1 could trigger the immune system to react to invaders which may pass through parietal hurt after the injury. Thus one amino acid substitution has resulted in shift of recognition strategy in the fruit fly, and allow the host to fight against a much broader spectrum of microorganisms. Combined reported anti-immune strategies of microbial to PAMP and DAMP, strong dimorphic haplotype and functional differentiation of the two major PGRP-SD alleles suggested that they are under balancing selection. As effector of innate immunity, antimicrobial peptides play an important role in killing invading microorganisms. Numerous antimicrobial peptides have been identified from amphibians which are mainly secreted by skin. From two skin cDNA libraries of two individuals of the Chinese red belly toad (Bombina maxima), we identified 56 different antimicrobial peptide cDNA sequences, each of which encodes a precursor peptide that can give rise to two kinds of antimicrobial peptides, maximin and maximin H. Among these cDNA, we found that the mean number of nucleotide substitution per non-synonymous site in both the maximin and maximin H domains significantly exceed the mean number of nucleotide substitution per synonymous site, whereas the same pattern was not observed in other structural regions, such as the signal and propiece peptide regions, suggesting that these antimicrobial peptide genes have been experiencing rapid diversification driven by overdominant selection. We cloned and sequenced seven genes amplified from skin or liver genomic DNA. These genes have three exons and share the same gene structure, in which both maximin and maximin H are encoded by the third exon. This suggests that alternative splicing and somatic recombination are less likely to play a role in creating the diversity of maximins and maximin Hs. The gene trees based on different domain regions revealed that domain shuffling and/or gene conversion among these genes might have happened frequently. |
语种 | 中文 |
公开日期 | 2010-10-15 |
源URL | [http://159.226.149.42:8088/handle/152453/6277] ![]() |
专题 | 昆明动物研究所_基因起源组 |
推荐引用方式 GB/T 7714 | 李岩. 天然免疫相关分子的进化[D]. 北京. 中国科学院研究生院. 2008. |
入库方式: OAI收割
来源:昆明动物研究所
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