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转座酶驯化的功能指征 - 人源性 piggyBac 转座酶衍生(PGBD)活性的特征。

Functional indications for transposase domestications - Characterization of the human piggyBac transposase derived (PGBD) activities.

机构信息

Institute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary.

Institute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary; Doctoral School of Biology, Institute of Biology, ELTE Eötvös Loránd University, Budapest, Hungary.

出版信息

Gene. 2022 Aug 5;834:146609. doi: 10.1016/j.gene.2022.146609. Epub 2022 May 21.

Abstract

Transposable elements are widespread in all living organisms. In addition to self-reproduction, they are a major source of genetic variation that drives genome evolution but our knowledge of the functions of human genes derived from transposases is limited. There are examples of transposon-derived, domesticated human genes that lost (SETMAR) or retained (THAP9) their transposase activity, however, several remnants in the human genome have not been thoroughly investigated yet. These include the five human piggyBac-derived sequences (PGBD1-5) which share ancestry with the Trichoplusia ni originated piggyBac (PB) transposase. Since PB is widely used in gene delivery applications, the potential activities of endogenous PGBDs are important to address. However, previous data is controversial, especially with the claimed transposition activity of PGBD5, it awaits further investigations. Here, we aimed to systematically analyze all five human PGBD proteins from several aspects, including phylogenetic conservation, potential transposase activity, expression pattern and their regulation in different stress conditions. Among PGBDs, PGBD5 is under the highest purifying selection, and exhibits the most cell type specific expression pattern. In a two-component vector system, none of the human PGBDs could mobilize either the insect PB transposon or the endogenous human PB-like MER75 and MER85 elements with intact terminal sequences. When cells were exposed to various stress conditions, including hypoxia, oxidative or UV stress, the expression profiles of all PGBDs showed different, often cell type specific responses; however, the pattern of PGBD5 in most cases had the opposite tendency than that of the other piggyBac-derived elements. Taken together, our results indicate that human PGBD elements did not retain their mobilizing activity, but their cell type specific, and cellular stress related expression profiles point toward distinct domesticated functions that require further characterization.

摘要

转座元件广泛存在于所有生物中。除了自我复制外,它们还是遗传变异的主要来源,驱动着基因组的进化,但我们对源自转座酶的人类基因的功能知之甚少。虽然有一些转座子衍生的、驯化的人类基因失去(SETMAR)或保留(THAP9)了它们的转座酶活性,但人类基因组中仍有几个残基尚未得到彻底研究。其中包括 5 个人类 piggyBac 衍生序列(PGBD1-5),它们与源自 Trichoplusia ni 的 piggyBac(PB)转座酶有亲缘关系。由于 PB 广泛应用于基因传递应用,因此内源性 PGBD 的潜在活性非常重要。然而,以前的数据存在争议,尤其是 PGBD5 的转座活性,它需要进一步研究。在这里,我们旨在从几个方面系统地分析所有 5 个人类 PGBD 蛋白,包括系统发育保守性、潜在转座酶活性、表达模式及其在不同应激条件下的调节。在 PGBDs 中,PGBD5 受到最高的纯化选择,表现出最细胞类型特异性的表达模式。在一个两组件载体系统中,没有一个人类 PGBD 能够动员昆虫 PB 转座子或内源性人类 PB 样 MER75 和 MER85 元件,这些元件具有完整的末端序列。当细胞暴露于各种应激条件下,包括缺氧、氧化或 UV 应激时,所有 PGBD 的表达谱表现出不同的、通常是细胞类型特异性的反应;然而,PGBD5 的模式在大多数情况下与其他 piggyBac 衍生元素的趋势相反。总之,我们的结果表明,人类 PGBD 元件没有保留它们的动员活性,但它们的细胞类型特异性和与细胞应激相关的表达模式表明了它们具有独特的驯化功能,需要进一步表征。

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