bioRxiv · 10.1101/2024.07.13.603364
Maintenance of long-term transposable element activity in genomes through regulation by nonautonomous elements
Abstract
Transposable elements are DNA sequences that can move and replicate within genomes. Broadly, there are two types: autonomous elements, which encode the necessary enzymes for transposition, and nonautonomous elements which rely on the enzymes produced by autonomous elements for their transposition. Nonautonomous elements have been proposed to regulate the numbers of transposable elements, which is a possible explanation for the persistence of transposition activity over long evolutionary times. However, previous modeling studies indicate that interactions between autonomous and nonautonomous elements usually result in the extinction of one type. Here, we study a stochastic model that allows for the stable coexistence of autonomous and nonautonomous retrotransposons. We determine the conditions for this coexistence and derive an analytical expression for the stationary distribution of their copy numbers, showing that nonautonomous elements regulate stochastic fluctuations and the number of autonomous elements in stationarity. We find that the stationary variances of each element can be expressed as a function of the average copy numbers and their covariance, enabling data comparison and model validation. These results suggest that continued transposition activity of transposable elements, regulated by nonautonomous elements, is a possible evolutionary outcome that could for example explain the long co-evolutionary history of autonomous LINE1 and nonautonomous Alu element transposition in the human ancestry.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Omole, A. D., Czuppon, P.. 2024-07-17. Maintenance of long-term transposable element activity in genomes through regulation by nonautonomous elements. https://doi.org/10.1101/2024.07.13.603364
Cite the original work for its findings. Save a collection to share your selection of sources.