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However, no such mobile element has been detected despite complete sequencing of the human and other vertebrate genomes and extensive, focused analysis of these sequences [6], [7].
Such localization of all flagellum-associated genes on a potentially mobile element has not been reported previously in either the Bacteria or the Archaea.
This suggests the possibility that these may reflect real transcripts in which a mobile element has been inserted into the genome.
This mobile element has inserted into the first intron of the Indy gene, and we show that it is often maintained in a heterozygous state.
Likewise, comparing G+C contents between the core chromosome and a putative mobile element is inconclusive when the recipient's chromosome and the mobile element shared a similar G+C content at the time of the horizontal transfer, or when the G+C content of the mobile element has progressively adapted to that of the recipient, a process called homing [ 10].
Similar(55)
Still more recently, new superfamilies, and completely new types of mobile element have been discovered [ 18, 19].
At least two different types of mobile element have been involved in these genetic exchanges on at least two different occasions.
The heterogeneous distribution of mobile elements has impacted the diversification of O26:H11 more than other EHEC 2 serotypes.
Current knowledge of distribution and evolution of this group of mobile elements has been mainly obtained from diverse model organisms [ 3].
Some large scale gene sharing between very different mobile entities (i.e., viruses and capsidless mobile elements) has recently been described elsewhere (Desnues et al. 2012; Yutin et al. 2013) giving rise to the concept of a mobilome network.
Exposure of organisms to high pressure has resulted in such mobilisation of transposable elements (Aertsen & Michiels, 2005; Lin et al., 2006), and alteration of methylation patterns of mobile elements has also been reported following hydrostatic pressurisation (Long et al., 2006).
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