Birth, Death, and Diversification of Mobile Promoters in Prokaryotes

A previous study of prokaryotic genomes identified large reservoirs of putative mobile promoters (PMPs), that is, homologous promoter sequences associated with nonhomologous coding sequences. Here we extend this data set to identify the full complement of mobile promoters in sequenced prokaryotic ge...

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Published inGenetics (Austin) Vol. 197; no. 1; pp. 291 - 299
Main Authors van Passel, Mark W J, Nijveen, Harm, Wahl, Lindi M
Format Journal Article
LanguageEnglish
Published United States Genetics Society of America 01.05.2014
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Summary:A previous study of prokaryotic genomes identified large reservoirs of putative mobile promoters (PMPs), that is, homologous promoter sequences associated with nonhomologous coding sequences. Here we extend this data set to identify the full complement of mobile promoters in sequenced prokaryotic genomes. The expanded search identifies nearly 40,000 PMP sequences, 90% of which occur in noncoding regions of the genome. To gain further insight from this data set, we develop a birth–death–diversification model for mobile genetic elements subject to sequence diversification; applying the model to PMPs we are able to quantify the relative importance of duplication, loss, horizontal gene transfer (HGT), and diversification to the maintenance of the PMP reservoir. The model predicts low rates of HGT relative to the duplication and loss of PMP copies, rapid dynamics of PMP families, and a pool of PMPs that exist as a single copy in a genome at any given time, despite their mobility. We report evidence of these “singletons” at high frequencies in prokaryotic genomes. We also demonstrate that including selection, either for or against PMPs, was not necessary to describe the observed data.
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Supporting information is available online at http://www.genetics.org/lookup/suppl/doi:10.1534/genetics.114.162883/-/DC1.
Current address: National Institute for Public Health, Centre for Infectious Disease Control, P.O. Box 1, 3720 BA Bilthoven, the Netherlands
ISSN:1943-2631
0016-6731
1943-2631
DOI:10.1534/genetics.114.162883