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Recurrent acquisition of cytosine methyltransferases into eukaryotic retrotransposons

Author

Listed:
  • Alex de Mendoza

    (The University of Western Australia
    Harry Perkins Institute of Medical Research)

  • Amandine Bonnet

    (Hôpital St. Louis)

  • Dulce B. Vargas-Landin

    (The University of Western Australia
    Harry Perkins Institute of Medical Research)

  • Nanjing Ji

    (Xiamen University)

  • Hongfei Li

    (Xiamen University)

  • Feng Yang

    (Xiamen University)

  • Ling Li

    (Xiamen University)

  • Koichi Hori

    (Tokyo Institute of Technology)

  • Jahnvi Pflueger

    (The University of Western Australia
    Harry Perkins Institute of Medical Research)

  • Sam Buckberry

    (The University of Western Australia
    Harry Perkins Institute of Medical Research)

  • Hiroyuki Ohta

    (Tokyo Institute of Technology)

  • Nedeljka Rosic

    (Southern Cross University
    The University of Queensland)

  • Pascale Lesage

    (Hôpital St. Louis)

  • Senjie Lin

    (Xiamen University
    University of Connecticut
    University of Connecticut)

  • Ryan Lister

    (The University of Western Australia
    Harry Perkins Institute of Medical Research)

Abstract

Transposable elements are in a constant arms race with the silencing mechanisms of their host genomes. One silencing mechanism commonly used by many eukaryotes is dependent on cytosine methylation, a covalent modification of DNA deposited by C5 cytosine methyltransferases (DNMTs). Here, we report how two distantly related eukaryotic lineages, dinoflagellates and charophytes, have independently incorporated DNMTs into the coding regions of distinct retrotransposon classes. Concomitantly, we show that dinoflagellates of the genus Symbiodinium have evolved cytosine methylation patterns unlike any other eukaryote, with most of the genome methylated at CG dinucleotides. Finally, we demonstrate the ability of retrotransposon DNMTs to methylate CGs de novo, suggesting that retrotransposons could self-methylate retrotranscribed DNA. Together, this is an example of how retrotransposons incorporate host-derived genes involved in DNA methylation. In some cases, this event could have implications for the composition and regulation of the host epigenomic environment.

Suggested Citation

  • Alex de Mendoza & Amandine Bonnet & Dulce B. Vargas-Landin & Nanjing Ji & Hongfei Li & Feng Yang & Ling Li & Koichi Hori & Jahnvi Pflueger & Sam Buckberry & Hiroyuki Ohta & Nedeljka Rosic & Pascale Le, 2018. "Recurrent acquisition of cytosine methyltransferases into eukaryotic retrotransposons," Nature Communications, Nature, vol. 9(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03724-9
    DOI: 10.1038/s41467-018-03724-9
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