These results and ours confirms, also for prokaryotes, previous findings that highly expressed genes appear to evolve slowly [ 35, 41].
Several of these loci appear to evolve under positive selection and many are also likely to exhibit functionally important polymorphism and local adaptation.
Exploits appear to evolve, with increasing levels of sophistication, in order to target multiple victims.
With crests exposed, PBRs appear to evolve into scalloped terrain due to abrasion.
In general, tRNA genes appear to evolve rapidly.
While the region is fast evolving it does not appear to evolve as fast as mitochondrial DNA.
They also appear to have evolved new ways of generating different kinds of bodies.
In response, host species also appear to have evolved their TRIM5α proteins, especially the coiled-coil and B30.2 PRYSPRY) domains, against retro- and lentiviruses [14], [15].
They also appear to have evolved much more slowly than agamid and chamaeleonid counterparts as judged from relatively short branch lengths within Iguanidae (Fig. 3).
H. pylori proteins with the greatest number of interactions also appear to have evolved slower on average between strains than the majority of the proteins.
