Microbiology Department, Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, University of Paris-Sud, Université Paris-Saclay, Gif-sur-Yvette cedex, France.
Unité de Biologie Moléculaire du Gène chez les Extrêmophiles, Département de Microbiologie, Institut Pasteur, Paris, France.
Mol Biol Evol. 2020 Jun 1;37(6):1727-1743. doi: 10.1093/molbev/msaa041.
Mobile genetic elements (MGEs) often encode integrases which catalyze the site-specific insertion of their genetic information into the host genome and the reverse reaction of excision. Hyperthermophilic archaea harbor integrases belonging to the SSV-family which carry the MGE recombination site within their open reading frame. Upon integration into the host genome, SSV integrases disrupt their own gene into two inactive pseudogenes and are termed suicidal for this reason. The evolutionary maintenance of suicidal integrases, concurring with the high prevalence and multiples recruitments of these recombinases by archaeal MGEs, is highly paradoxical. To elucidate this phenomenon, we analyzed the wide phylogenomic distribution of a prominent class of suicidal integrases which revealed a highly variable integration site specificity. Our results highlighted the remarkable hybrid nature of these enzymes encoded from the assembly of inactive pseudogenes of different origins. The characterization of the biological properties of one of these integrases, IntpT26-2 showed that this enzyme was active over a wide range of temperatures up to 99 °C and displayed a less-stringent site specificity requirement than comparable integrases. These observations concurred in explaining the pervasiveness of these suicidal integrases in the most hyperthermophilic organisms. The biochemical and phylogenomic data presented here revealed a target site switching system operating on highly thermostable integrases and suggested a new model for split gene reconstitution. By generating fast-evolving pseudogenes at high frequency, suicidal integrases constitute a powerful model to approach the molecular mechanisms involved in the generation of active genes variants by the recombination of proto-genes.
移动遗传元件(MGEs)通常编码整合酶,这些酶催化它们的遗传信息特异地插入宿主基因组和反向的切除反应。高温古菌含有属于 SSV 家族的整合酶,其 MGE 重组位点位于开放阅读框内。整合到宿主基因组后,SSV 整合酶会将自身基因断裂成两个无活性的假基因,因此被称为自杀性。自杀性整合酶的进化维持,与这些重组酶在古菌 MGE 中的高普遍性和多重招募相吻合,是非常矛盾的。为了阐明这一现象,我们分析了一类重要的自杀性整合酶的广泛系统发育基因组分布,揭示了高度可变的整合位点特异性。我们的研究结果强调了这些酶的显著混合性质,它们是由不同来源的无活性假基因组装而成的。对其中一种整合酶 IntpT26-2 的生物学特性进行了表征,结果表明该酶在 99°C 以下的宽温度范围内具有活性,并表现出比类似整合酶更宽松的位点特异性要求。这些观察结果共同解释了这些自杀性整合酶在最嗜热生物中的普遍性。这里呈现的生化和系统发育基因组数据揭示了一种在高度耐热整合酶上起作用的靶标位点转换系统,并提出了一种新的分裂基因重组模型。通过以高频率产生快速进化的假基因,自杀性整合酶构成了一个强大的模型,可以用来研究通过原基因重组产生活性基因变异的分子机制。