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Inteins introns and homing endonucleases: recent revelations about the life cycle of parasitic genetic elements

机译:内含子内含子和归巢核酸内切酶:关于寄生遗传元件生命周期的最新启示

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摘要

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.
机译:依靠归巢核酸内切酶进行繁殖的自剪接内含子和内含子是寄生遗传元件。它们的生命周期和进化命运已通过归巢周期进行了描述。根据该模型,仅在寄生虫扩散阶段才选择归巢核酸内切酶以发挥功能。当寄生元素固定在总体中时,此阶段结束。固定后,归巢核酸内切酶不再处于选择状态,其活性通过随机过程丧失。最近对具有功能性归巢核酸内切酶的这些寄生元件的分析表明,这种模型以其最简单的形式并不总是适用。显然,功能正常的内切核酸酶可以在被认为是无性或近乎无性的种群和物种中持续较长的进化时间。在这里,我们回顾这些最新发现并讨论其含义。功能性归巢核酸内切酶长期存在的原因包括:与这些生物体相比,重组(性和基因转移的结果)重组程度更高;复杂的人口结构,阻碍了这一要素的固定;归巢核酸内切酶的主动传播与宿主生物中的寄生虫引起的适应性下降之间的平衡;或归巢核酸内切酶的功能,可以提高宿主生物的适应性,甚至在固定在本地人群中后,也可以纯化对归巢核酸内切酶活性的选择。将来,需要对种群内归巢核酸酶活性和调控动力学进行更详细的研究,以确定这些可能性之间的关系,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Naegleria I类内含子(Wikmark等人BMC Evol Biol 2006,> 6: 39)和子囊虫中PRP8内含子的两篇杰出著作(Butler等人BMC Evol Biol 2006,> 6: 42)提供了重要的踏脚石,可用于综合研究这些寄生元素如何随其宿主一起(或不管宿主如何)随时间演变。

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