Abstract

piRNA clusters are thought to repress transposable element (TE) activity in mammals and invertebrates. Here, we show that a simple population genetics model reveals a constraint on the size of piRNA clusters: The total size of the piRNA clusters of an organism must exceed 0.2% of a genome to repress TE invasions. Moreover, larger piRNA clusters accounting for up to 3% of the genome may be necessary when populations are small, transposition rates are high, and TE insertions are recessive. If piRNA clusters are too small, the load of deleterious TE insertions that accumulate during a TE invasion may drive populations extinct before an effective piRNA-based defense against the TE can be established. Our findings are solely based on three well-supported assumptions: 1) TEs multiply within genomes, 2) TEs are mostly deleterious, and 3) piRNA clusters act as transposon traps, where a single insertion in a cluster silences all TE copies in trans. Interestingly, the piRNA clusters of some species meet our observed minimum size requirements, whereas the clusters of other species do not. Species with small piRNA clusters, such as humans and mice, may experience severe fitness reductions during invasions of novel TEs, which is possibly even threatening the persistence of some populations. This work also raises the important question of how piRNA clusters evolve. We propose that the size of piRNA clusters may be at an equilibrium between evolutionary forces that act to expand and contract piRNA clusters.

Highlights

  • Transposable elements (TEs) are short stretches of DNA that selfishly propagate within genomes (Orgel and Crick, 1980; Doolittle and Sapienza, 1980)

  • The trap model holds that the proliferation of an invading TE is stopped when a TE copy jumps into a piRNA cluster, which triggers the production of piRNAs that silence all TE copies in trans

  • We measured the size of piRNA clusters in percent of a genome, since we previously found that the relative size of piRNA clusters, and not the absolute size, determines invasion dynamics of TEs (Kofler, 2019)

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Summary

Introduction

Transposable elements (TEs) are short stretches of DNA that selfishly propagate within genomes (Orgel and Crick, 1980; Doolittle and Sapienza, 1980). Negative effect of TEs may arise by three mechanisms: i) ectopic recombination among TEs could lead to deleterious chromosomal rearrangements ii) TE insertions may have direct negative effects, for example by disrupting genes or regulatory regions and iii) the products of TEs, such as the Transposase, could generate deleterious effects (e.g. DNA breaks) (Nuzhdin, 1999; Montgomery et al, 1991) Despite this largely selfish activity some TE insertions may confer beneficial effects to hosts, such as resistance to insecticides (Gonzalez et al, 2008; Casacuberta and Gonzalez, 2013; Daborn et al, 2002).

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