Sentence examples for retention during evolution from inspiring English sources

A unique feature of the T. vaginalis genome is the retention during evolution of multiple paralogous copies for a majority of all genes.

Various mechanisms have been postulated to explain TSGD paralogue retention during evolution including mutations leading to differential regulation in expression (sub-functionalization) and/or the evolution of some novel function (neofunctionalization) [ 36].

Partitioning of duplicate gene expression in response to environmental stress may lead to duplicate gene retention during subsequent evolution (Liu and Adam [2007]).

Genomic and transcriptomic studies have improved our understanding of phytochrome loss, retention, and diversification during evolution.

Gene gain and subsequent retention or loss during evolution may be one of the underlying mechanisms involved in generating the diversity of metazoan nervous systems.

This could be due to polyploidization followed by selective gene loss [ 29, 16, 28] resulting in retention of a single copy during evolution of Saccharum.

One of the hypotheses that has been proposed to explain retention of functionally redundant paralogs during evolution is a contribution to gene dosage and, thereby, to the capacity of the pathway or process in which they operate (97, 98).

We propose that minor introns are control switches that are regulated by U6atac abundance, providing a novel gene expression regulation mechanism and explaining the retention of the minor splicing pathway during evolution.

The specific acquisition of PsGEF by the last common ancestor of protostomes followed by the retention or loss in specific animal species during evolution demonstrates that there are some structural and/or functional features common between insect and lophotrochozoan nervous systems (for example, MBs), which are absent in all deuterostomes and cnidarians.

The specific acquisition of PsGEF by the last common ancestor of protostomes followed by the retention or loss in specific animal species during evolution demonstrates that there are some structural and/or functional features common between insect and lophotrochozoan nervous systems, which are absent in all deuterostomes and cnidarians.

The specific acquisition of PsGEF by the last common ancestor of protostomes followed by its retention or loss in specific animal species during evolution demonstrates that there are some structural and/or functional features common between insect and lophotrochozoan nervous systems (for example, mushroom bodies), which are absent in all deuterostomes and cnidarians.