Victorian Infectious Diseases Service, Royal Melbourne Hospital, Parkville, Vic., Australia; Department of Medicine, Royal Melbourne Hospital, University of Melbourne, Parkville, Vic., Australia.
Clin Exp Immunol. 2014 May;176(2):165-71. doi: 10.1111/cei.12241.
Either immune selection or stochastic processes may have influenced the frequency of highly polymorphic genes such as mannose-binding lectin 2 (MBL2). This pattern recognition receptor of the innate immune system recognizes and binds to pathogenic microorganisms and apoptotic cells leading to lectin pathway complement killing or clearance. In almost all of a large number of studies in different ethnic groups worldwide there is 20-25% carriage of low MBL2 haplotypes, with 8-10% of each population having no MBL detectable in the blood. The source of this high variability of MBL2 remains cryptic. It arises from six main snps in the prompter and exon regions of the gene that assort into seven common haplotypes under linkage disequilibrium. While global studies of MBL2 show that it is not under immune selection pressure, these results are not the same when the same population genetic tools are used on large national studies. Other analyses point to the silenced MBL1 pseudogene and development of promoter polymorphisms in humans as evidence of selection pressure favouring low-producing haplotypes. While these analyses cannot be reconciled readily, there are two processes by which MBL heterozygosity could have been advantageous in an evolutionary sense; protection against adverse effects of various infectious diseases and lethal manifestations of atherosclerosis - a disease that now seems to have a more ancient history than assumed previously. Ultimately, consideration of the context for possible future therapeutic manipulation of MBL means that this can proceed independently of resolution of the evolutionary forces that have shaped MBL2 polymorphism.
无论是免疫选择还是随机过程,都可能影响到高度多态基因(如甘露糖结合凝集素 2(MBL2))的频率。这种先天免疫系统的模式识别受体识别并结合致病微生物和凋亡细胞,导致凝集素途径补体杀伤或清除。在全球不同种族的大量研究中,几乎所有研究都表明 20-25%的人携带低 MBL2 单倍型,其中 8-10%的人群血液中无法检测到 MBL。MBL2 高度变异性的来源仍然是个谜。它源自基因启动子和外显子区域的六个主要单核苷酸多态性,在连锁不平衡下分为七种常见单倍型。虽然全球 MBL2 研究表明它不受免疫选择压力的影响,但当在大型国家研究中使用相同的群体遗传工具时,这些结果并不相同。其他分析表明,沉默的 MBL1 假基因和启动子多态性的发展是选择压力有利于低产单倍型的证据。虽然这些分析不容易调和,但 MBL 杂合性在进化意义上可能具有优势的两种过程是:保护免受各种传染病的不利影响和动脉粥样硬化的致命表现——这种疾病现在似乎比以前假设的历史更悠久。最终,考虑到未来可能对 MBL 进行治疗干预的背景,这可以独立于塑造 MBL2 多态性的进化力量的解决而进行。