TY - JOUR
T1 - Recurrent acquisition of cytosine methyltransferases into eukaryotic retrotransposons
AU - de Mendoza, Alex
AU - Bonnet, Amandine
AU - Vargas-Landin, Dulce B.
AU - Ji, Nanjing
AU - Li, Hongfei
AU - Yang, Feng
AU - Li, Ling
AU - Hori, Koichi
AU - Pflueger, Jahnvi
AU - Buckberry, Sam
AU - Ohta, Hiroyuki
AU - Rosic, Nedeljka
AU - Lesage, Pascale
AU - Lin, Senjie
AU - Lister, Ryan
PY - 2018/5/1
Y1 - 2018/5/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85045200840&partnerID=8YFLogxK
U2 - 10.1038/s41467-018-03724-9
DO - 10.1038/s41467-018-03724-9
M3 - Article
C2 - 29632298
AN - SCOPUS:85045200840
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 1341
ER -