Abstract

Transposable elements (TEs) are ubiquitous in both prokaryotes and eukaryotes, and the dynamic character of their interaction with host genomes brings about numerous evolutionary innovations and shapes genome structure and function in a multitude of ways. In traditional classification systems, TEs are often being depicted in simplistic ways, based primarily on the key enzymes required for transposition, such as transposases/recombinases and reverse transcriptases. Recent progress in whole-genome sequencing and long-read assembly, combined with expansion of the familiar range of model organisms, resulted in identification of unprecedentedly long transposable units spanning dozens or even hundreds of kilobases, initially in prokaryotic and more recently in eukaryotic systems. Here, we focus on such oversized eukaryotic TEs, including retrotransposons and DNA transposons, outline their complex and often combinatorial nature and closely intertwined relationship with viruses, and discuss their potential for participating in transfer of long stretches of DNA in eukaryotes.

Highlights

  • The distinguishing characteristic of transposable elements (TEs), or mobile genetic elements (MGEs), is the ability to change their chromosomal location, within, and between genomes, as well as between species or even higher-order taxa

  • Evolution of the simplistic views on eukaryotic TE organization gradually led to realization of their largely modular structure, whereby INs of different types may be combined with different replicases and diverse accessory functions to achieve mobilization of DNA segments of increasing size ranges

  • Successful domain combinations may emerge at any point in evolution: Early emergence leads to more widespread taxonomic distribution, whereas taxon-specific combinations may be able to spread either vertically or horizontally

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Summary

Introduction

The distinguishing characteristic of transposable elements (TEs), or mobile genetic elements (MGEs), is the ability to change their chromosomal location, within, and between genomes, as well as between species or even higher-order taxa. This view has drastically changed with the realization that, in the context of whole-genome sequence, some of the 6-kb RT-encoding mobile units in cloned telomeres of bdelloid rotifers (Gladyshev and Arkhipova 2007) represented only the 30-terminal fragments of giant retroelements up to 40 kb in length (Arkhipova et al 2017) (Fig. 2D) These EN-deficient elements, in addition to RT, can accommodate a variety of accessory functions, such as DEDDy 30exonucleases, GDSL esterases/lipases, GIY-YIG-like ENs, rolling-circle replication initiator (Rep) proteins, and putatively structural ORFs with coiled-coil motifs and transmembrane domains. There may be only a short window of time for bona fide HGT mediated by TEs to be identified

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