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Gene trees from various species showed that intraspecific duplicates evolve in concert, perhaps through frequent gene conversion, although this does not prevent sequence divergence, especially where structural heterogeneity physically separates a duplicate from its neighbours.
Concerted evolution arises due to frequent gene conversion between paralogous genes.
And the sex/sex-related loci appear to have been subject to frequent gene conversion and translocations in microsporidia and zygomycetes.
To summarize, in contrast to the SPANX-A/D subfamily where frequent gene conversion events are a driving force of SPANX-A/D gene variantion in human populations [5], a normal polymorphism is characteristic for the evolutionary old SPANX-N subfamily.
Sequence identity within VCY is due to frequent gene conversion between palindrome arms [ 26, 27].
These findings strongly suggest that frequent gene conversion has taken place within the HEG sequence.
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The conclusion that both the whole BES and individual ESAGs are mosaics raises the question as to how it is possible for two contiguous markers, such as ESAG1 and 2, to display parallel evolutionary histories, when both gene families are being homogenised by frequent gene conversions.
Besides epigenetic switches, there is solid evidence for frequent gene conversions between VAR genes [ 9].
Here, we found frequent gene conversions in the evolutionary course of primates.
Frequent gene conversions between paralogs on the same chromosome are well known among the VCX and VCY genes.
Introns were lost preferentially from GC-rich regions, which is a characteristic of frequent gene conversions [ 62].
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