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RecA-independent Ectopic Transposition in Vivo of a Bacterial Group II Intron

Overview
Specialty Biochemistry
Date 2000 Nov 1
PMID 11058141
Citations 19
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Abstract

RmInt1 is a group II intron of Sinorhizobium meliloti which was initially found within the insertion sequence ISRm2011-2. Although the RmInt1 intron-encoded protein lacks a recognizable endonuclease domain, it is able to mediate insertion of RmInt1 at an intron-specific location in intronless ISRm2011-2 recipient DNA, a phenomenon termed homing. Here we have characterized three additional insertion sites of RmInt1 in the genome of S.meliloti. Two of these sites are within IS elements closely related to ISRm2011-2, which appear to form a characteristic group within the IS630-Tc1 family. The third site is in the oxi1 gene, which encodes a putative oxide reductase. The newly identified integration sites contain conserved intron-binding site (IBS1 and IBS2) and delta' sequences (14 bp). The RNA of the intron-containing oxi1 gene is able to splice and the oxi1 site is a DNA target for RmInt1 transposition in vivo. Ectopic transposition of RmInt1 into the oxi1 gene occurs at 20-fold lower efficiency than into the homing site (ISRm2011-2) and is independent of the major RecA recombination pathway. The possibility that transposition of RmInt1 to the oxi1 site occurs by reverse splicing into DNA is discussed.

Citing Articles

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Inactivation of group II intron RmInt1 in the Sinorhizobium meliloti genome.

Molina-Sanchez M, Toro N Sci Rep. 2015; 5:12036.

PMID: 26156864 PMC: 4496777. DOI: 10.1038/srep12036.


Mobile Bacterial Group II Introns at the Crux of Eukaryotic Evolution.

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Insights into the strategies used by related group II introns to adapt successfully for the colonisation of a bacterial genome.

Martinez-Rodriguez L, Garcia-Rodriguez F, Molina-Sanchez M, Toro N, Martinez-Abarca F RNA Biol. 2014; 11(8):1061-71.

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Alternative splicing of a group II intron in a surface layer protein gene in Clostridium tetani.

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