Gogarten J Peter, Hilario Elena
Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut 06269-31258, USA.
BMC Evol Biol. 2006 Nov 13;6:94. doi: 10.1186/1471-2148-6-94.
Self splicing introns and inteins that rely on a homing endonuclease for propagation are parasitic genetic elements. Their life-cycle and evolutionary fate has been described through the homing cycle. According to this model the homing endonuclease is selected for function only during the spreading phase of the parasite. This phase ends when the parasitic element is fixed in the population. Upon fixation the homing endonuclease is no longer under selection, and its activity is lost through random processes. Recent analyses of these parasitic elements with functional homing endonucleases suggest that this model in its most simple form is not always applicable. Apparently, functioning homing endonuclease can persist over long evolutionary times in populations and species that are thought to be asexual or nearly asexual. Here we review these recent findings and discuss their implications. Reasons for the long-term persistence of a functional homing endonuclease include: More recombination (sexual and as a result of gene transfer) than previously assumed for these organisms; complex population structures that prevent the element from being fixed; a balance between active spreading of the homing endonuclease and a decrease in fitness caused by the parasite in the host organism; or a function of the homing endonuclease that increases the fitness of the host organism and results in purifying selection for the homing endonuclease activity, even after fixation in a local population. In the future, more detailed studies of the population dynamics of the activity and regulation of homing endonucleases are needed to decide between these possibilities, and to determine their relative contributions to the long term survival of parasitic genes within a population. Two outstanding publications on the amoeba Naegleria group I intron (Wikmark et al. BMC Evol Biol 2006, 6:39) and the PRP8 inteins in ascomycetes (Butler et al.BMC Evol Biol 2006, 6:42) provide important stepping stones towards integrated studies on how these parasitic elements evolve through time together with, or despite, their hosts.
依赖归巢内切酶进行传播的自我剪接内含子和蛋白质内含子是寄生性遗传元件。它们的生命周期和进化命运已通过归巢循环得以描述。根据该模型,归巢内切酶仅在寄生虫的传播阶段因功能而被选择。当寄生元件在种群中固定下来时,这个阶段就结束了。固定之后,归巢内切酶不再处于选择之下,其活性通过随机过程丧失。最近对这些具有功能性归巢内切酶的寄生元件的分析表明,这种最简单形式的模型并非总是适用。显然,功能性归巢内切酶能够在被认为是无性或近乎无性的种群和物种中长时间持续存在。在此,我们综述这些最新发现并讨论其意义。功能性归巢内切酶长期持续存在的原因包括:这些生物体的重组(有性重组以及基因转移导致的重组)比之前所认为的更多;复杂的种群结构阻止了元件的固定;归巢内切酶的活跃传播与寄生虫在宿主生物体中导致的适应性降低之间的平衡;或者归巢内切酶的一种功能,这种功能提高了宿主生物体的适应性,并导致对归巢内切酶活性进行纯化选择,即使在局部种群中固定之后也是如此。未来,需要对归巢内切酶活性和调控的种群动态进行更详细的研究,以在这些可能性之间做出抉择,并确定它们对种群内寄生基因长期存活的相对贡献。关于变形虫纳格里亚属I类内含子(Wikmark等人,《BMC进化生物学》2006年,6:39)和子囊菌中的PRP8蛋白质内含子(Butler等人,《BMC进化生物学》2006年,6:42)的两篇杰出论文为综合研究这些寄生元件如何与宿主一起或不顾宿主而随时间进化提供了重要的基石。