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and Metastriata (R. sanguineus, Amblyomma triguttatum, Haemaphysalis flava) could be linked to mt gene arrangements [ 37, 38].
Mt gene arrangements have already provided strong support toward the resolution of several long-standing controversial phylogenetic relationships [ 12].
Their findings indicated that mt gene arrangements of myctophid fishes have the potential to provide evidence concerning clade delimitation at various levels.
The mt gene arrangements of almost all archaeobatrachians so far reported (excluding the Leiopelma archeyi mt genome [ 43]) are identical to the typical vertebrate-type arrangement (e.g., [ 9] and Figure 1]).
Mapping the distribution of mt gene arrangements onto a taxonomically comprehensive phylogeny of Octocorallia suggests that all of the known octocoral gene orders have evolved by successive inversions of one or more evolutionarily conserved blocks of protein-coding genes.
The mt gene arrangements of L. entomophila and L. paeta differ from that of the hypothetical ancestor of insects, from that of the other booklice and from each other.
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Here, we document an additional genus of octocoral with a novel mt gene arrangement.
Almost all basal anurans (= archaeobatrachians, excluding Leiopelma with nd6 and trnP translocations [ 43]) have the vertebrate-type mt gene arrangement.
This result is consistent with the previous studies [ 17, 21, 23] and can be concluded by mt gene arrangement analyses.
In the human head louse and the human body louse, atp8-atp6 is the only ancestral mt gene arrangement of insects retained (Shao et al. 2009, 2012).
Mitochondrial (mt) gene arrangement has been highly conserved among vertebrates from jawless fishes to mammals for more than 500 million years.
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