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真核反转录转座子中胞嘧啶甲基转移酶的反复获得。

Recurrent acquisition of cytosine methyltransferases into eukaryotic retrotransposons.

机构信息

Australian Research Council Centre of Excellence in Plant Energy Biology, School of Molecular Sciences, The University of Western Australia, Perth, WA, 6009, Australia.

Harry Perkins Institute of Medical Research, Perth, WA, 6009, Australia.

出版信息

Nat Commun. 2018 Apr 9;9(1):1341. doi: 10.1038/s41467-018-03724-9.

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.

摘要

转座元件与宿主基因组的沉默机制处于持续的军备竞赛中。许多真核生物常用的一种沉默机制依赖于胞嘧啶甲基化,这是由 C5 胞嘧啶甲基转移酶(DNMTs)催化的 DNA 共价修饰。在这里,我们报告了两个远缘真核生物谱系——甲藻和轮藻——如何独立地将 DNMT 整合到不同反转录转座子类别的编码区中。同时,我们表明,属共生甲藻的甲藻已经进化出了不同于任何其他真核生物的胞嘧啶甲基化模式,大多数基因组在 CG 二核苷酸处被甲基化。最后,我们证明了反转录转座子 DNMT 能够从头甲基化 CG,这表明反转录转座子可以自我甲基化反转录的 DNA。总之,这是一个反转录转座子整合参与 DNA 甲基化的宿主衍生基因的例子。在某些情况下,这种事件可能会影响宿主表观基因组环境的组成和调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a692/5890265/e636b044ec62/41467_2018_3724_Fig1_HTML.jpg

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