首页> 外文期刊>Journal of Molecular Biology >The piggyBac-derived protein 5 (PGBD5) transposes both the closely and the distantly related piggyBac-like elements Tcr-pble and Ifp2
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The piggyBac-derived protein 5 (PGBD5) transposes both the closely and the distantly related piggyBac-like elements Tcr-pble and Ifp2

机译:PiggyBac衍生的蛋白5(PGBD5)(PGBD5)紧密地传递,并且恒定相关的贪污物质TCR-PBE和IFP2

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摘要

The vertebrate piggyBac derived transposase 5 (PGBD5) encodes a domesticated transposase, which is active and able to transpose its distantly related piggyBac-like element (pble), Ifp2. This raised the question whether PGBD5 would be more effective at mobilizing a phylogenetically closely related pble element. We aimed to identify the pble most closely related to the pgbd5 gene. We updated the landscape of vertebrate pgbd genes to develop efficient filters and identify the most closely related pble to each of these genes. We found that Tcr-pble is phylogenetically the closest pble to the pgbd5 gene. Furthermore, we evaluated the capacity of two murine and human PGBD5 isoforms, Mm523 and Hs524, to transpose both Tcr-pble and Ifp2 elements. We found that both pbles could be transposed by Mm523 with similar efficiency. However, integrations of both pbles occurred through both proper transposition and improper PGBD5-dependent recombination. This suggested that the ability of PGBD5 to bind both pbles may not be based on the primary sequence of element ends, but may involve recognition of inner DNA motifs, possibly related to palindromic repeats. In agreement with this hypothesis, we identified internal palindromic repeats near the end of 24 pble sequences, which display distinct sequences. (C) 2021 Elsevier Ltd. All rights reserved.
机译:脊椎动物piggyBac衍生的转座酶5(PGBD5)编码一种驯化的转座酶,该转座酶是活跃的,能够转座其远亲的piggyBac样元件(pble),Ifp2。这就提出了一个问题,即PGBD5是否能更有效地动员与系统发育密切相关的pble元件。我们的目的是鉴定与pgbd5基因最密切相关的pble。我们更新了脊椎动物pgbd基因的布局,以开发有效的过滤器,并确定与这些基因最密切相关的pble。我们发现Tcr pble在系统发育上是最接近pgbd5基因的pble。此外,我们还评估了两种小鼠和人类PGBD5亚型Mm523和Hs524转座Tcr pble和Ifp2元件的能力。我们发现Mm523可以以相似的效率转置两个PBLE。然而,两种PBLE的整合都是通过适当的转位和不适当的PGBD5依赖性重组实现的。这表明PGBD5结合两个PBLE的能力可能不是基于元素末端的一级序列,而是可能涉及识别内部DNA基序,可能与回文重复有关。与这一假设一致,我们在24个pble序列的末端附近发现了内部回文重复序列,这些序列显示不同的序列。(c)2021爱思唯尔有限公司保留所有权利。

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