Background: Transposable element (TE) activity is generally deleterious to the host fitness, so that genomes often evolve TE control mechanisms, and TE copies are purged by recombination and selection. In the absence of recombination, the number of TE insertions usually increases, but the dynamics of such TE accumulations is unknown.
Results: In this study, we investigated the tempo of TE accumulation in the non-recombining genomic regions of 15 Microbotryum species, leveraging on a unique dataset of 21 independent evolutionary strata of recombination cessation of different ages in closely related species. We show that TEs have rapidly accumulated following recombination suppression but that the TE content reached a plateau at ca. 50% of occupied base pairs by 1.5 MY following recombination suppression. The same superfamilies repeatedly expanded in independently evolved non-recombining regions, and in particular Helitrons, despite being scarce before recombination
suppression. TEs from the most abundant elements, i.e., Copia and Ty3/Gypsy retrotransposon superfamilies, have also expanded independently in the different non-recombining regions. Copia and Ty3 retrotransposons have accumulated through bursts affecting both the non-recombining regions of the mating-type chromosomes and autosomes at the same time, which supports the TE reservoir hypothesis, i.e., that the TEs accumulated in non-recombining regions have a genome-wide impact by transposing to recombining regions.
Conclusion: This study sheds light on the genome-wide consequences of the accumulation of TEs in non-recombining regions, thus improving our knowledge on genome evolution.