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猪源 bac 蛋白 5(PGBD5)转座近源和远源的猪源 bac 样元件 Tcr-pble 和 Ifp2。

The piggyBac-derived protein 5 (PGBD5) transposes both the closely and the distantly related piggyBac-like elements Tcr-pble and Ifp2.

机构信息

UMR INRAE 0085, CNRS 7247, Physiologie de la Reproduction et des Comportements, Centre INRA Val de Loire, 37380 Nouzilly, France.

UMR MEPHI D-258, I, IRD, Aix Marseille Université, 19-21 Boulevard Jean Moulin, 13005 Marseille, France; CNRS SNC 5039, 13005 Marseille, France.

出版信息

J Mol Biol. 2021 Apr 2;433(7):166839. doi: 10.1016/j.jmb.2021.166839. Epub 2021 Feb 2.

Abstract

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.

摘要

脊椎动物衍生转座酶 5(PGBD5)编码一种驯化转座酶,该酶具有活性且能够转座其远缘的类似 piggyBac 元件(pble),Ifp2。这就提出了一个问题,即 PGBD5 是否更有效地动员系统发育上密切相关的 pble 元件。我们旨在确定与 pgbd5 基因最密切相关的 pble。我们更新了脊椎动物 pgbd 基因的景观,以开发有效的筛选方法并识别与这些基因中的每一个最密切相关的 pble。我们发现 Tcr-pble 在系统发育上与 pgbd5 基因最密切相关。此外,我们评估了两种鼠和人 PGBD5 同工型 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座这两个 pble。然而,这两个 pble 的整合都是通过适当的转座和 PGBD5 依赖性重组的不适当发生的。这表明 PGBD5 结合两个 pble 的能力可能不是基于元件末端的主要序列,而是可能涉及到对内部 DNA 基序的识别,可能与回文重复有关。与该假设一致,我们在 24 个 pble 序列的末端附近鉴定出内部回文重复序列,它们显示出不同的序列。

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