Abstract
Background"Domestication" of transposable elements (TEs) led to evolutionary breakthroughs such as the origin of telomerase and the vertebrate adaptive immune system. These breakthroughs were accomplished by the adaptation of molecular functions essential for TEs, such as reverse transcription, DNA cutting and ligation or DNA binding. Cryptons represent a unique class of DNA transposons using tyrosine recombinase (YR) to cut and rejoin the recombining DNA molecules. Cryptons were originally identified in fungi and later in the sea anemone, sea urchin and insects.ResultsHerein we report new Cryptons from animals, fungi, oomycetes and diatom, as well as widely conserved genes derived from ancient Crypton domestication events. Phylogenetic analysis based on the YR sequences supports four deep divisions of Crypton elements. We found that the domain of unknown function 3504 (DUF3504) in eukaryotes is derived from Crypton YR. DUF3504 is similar to YR but lacks most of the residues of the catalytic tetrad (R-H-R-Y). Genes containing the DUF3504 domain are potassium channel tetramerization domain containing 1 (KCTD1), KIAA1958, zinc finger MYM type 2 (ZMYM2), ZMYM3, ZMYM4, glutamine-rich protein 1 (QRICH1) and "without children" (WOC). The DUF3504 genes are highly conserved and are found in almost all jawed vertebrates. The sequence, domain structure, intron positions and synteny blocks support the view that ZMYM2, ZMYM3, ZMYM4, and possibly QRICH1, were derived from WOC through two rounds of genome duplication in early vertebrate evolution. WOC is observed widely among bilaterians. There could be four independent events of Crypton domestication, and one of them, generating WOC/ZMYM, predated the birth of bilaterian animals. This is the third-oldest domestication event known to date, following the domestication generating telomerase reverse transcriptase (TERT) and Prp8. Many Crypton-derived genes are transcriptional regulators with additional DNA-binding domains, and the acquisition of the DUF3504 domain could have added new regulatory pathways via protein-DNA or protein-protein interactions.ConclusionsCryptons have contributed to animal evolution through domestication of their YR sequences. The DUF3504 domains are domesticated YRs of animal Crypton elements.
Highlights
The structural and mechanistic variety of transposable elements (TEs) is well-documented [1]
Because of the low resolution of the phylogenetic tree, we could not determine whether there is any relationship between these four Crypton groups and to other tyrosine recombinase (YR)-encoding elements, and we cannot rule out the possibility that they have originated independently
The analysis of four MarCry-1_FO copies with more than 97% identity to each other revealed the presence of 16-bp terminal inverted repeat (TIR) and target site duplications (TSDs) of the TA dinucleotide, indicating that their Mariner-type DDE-transposase is responsible for transposition
Summary
The structural and mechanistic variety of transposable elements (TEs) is well-documented [1] They encode proteins that include diverse functional domains involved in catalysis or interaction with DNA, RNA and other proteins. Because of this diverse repertoire, TEs can supply functional modules to generate new genes. V(D)J recombination is a mechanism used in jawed vertebrates to generate a variety of immunoglobulins and T-cell receptors. It is catalyzed by the recombination activating gene 1 (RAG1) derived from a transposase encoded by the Transib family of DNA transposons [5]. We report in-depth studies of another type of transposon enzyme, tyrosine recombinase (YR), which was repeatedly domesticated in the history of animals
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