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Homing of a bacterial group II intron with an intron-encoded protein lacking a recognizable endonuclease domain.

机译:用缺乏可识别的核酸内切酶结构域的内含子编码蛋白将细菌II组内含子归巢。

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摘要

RmInt1 is a functional group II intron found in Sinorhizobium meliloti where it interrupts a group of IS elements of the IS630-Tc1 family. In contrast to many other group II introns, the intron-encoded protein (IEP) of RmInt1 lacks the characteristic conserved part of the Zn domain associated with the IEP endonuclease activity. Nevertheless, in this study, we show that RmInt1 is capable of inserting into a vector containing the DNA spanning the RmInt1 target site from the genome of S. meliloti. Efficient homing was also observed in the absence of homologous recombination (RecA- strains). In addition, it is shown that RmInt1 is able to move to its target in a heterologous host (S. medicae). Homing of RmInt1 occurs very efficiently upon DNA target uptake (conjugation/electroporation) by the host cell resulting in a proportion of invaded target of 11-30%. Afterwards, the remaining intronless target DNA is protected from intron invasion.
机译:RmInt1是在苜蓿中华根瘤菌中发现的II型功能内含子,在其中它干扰了IS630-Tc1家族的一组IS元件。与许多其他II组内含子相比,RmInt1的内含子编码蛋白(IEP)缺少与IEP核酸内切酶活性相关的Zn结构域的特征保守部分。然而,在这项研究中,我们表明RmInt1能够插入包含跨越S.meliloti基因组的RmInt1目标位点的DNA的载体中。在没有同源重组(RecA-菌株)的情况下,也观察到有效的归巢。此外,还显示RmInt1能够移至异源宿主(S. medicae)中的目标。 RmInt1归巢在宿主细胞吸收DNA靶标(结合/电穿孔)后非常有效,导致入侵靶标的比例为11-30%。之后,保护剩余的无内含子靶DNA免受内含子入侵。

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