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通过青鳉鱼体内大规模基因组工程和甲基化组编辑揭示甲基化组模式与核苷酸序列的解耦。

Unlinking the methylome pattern from nucleotide sequence, revealed by large-scale in vivo genome engineering and methylome editing in medaka fish.

作者信息

Cheung Napo K M, Nakamura Ryohei, Uno Ayako, Kumagai Masahiko, Fukushima Hiroto S, Morishita Shinichi, Takeda Hiroyuki

机构信息

Department of Biological Sciences, Graduate School of Science, The University of Tokyo, Tokyo, Japan.

Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo, Tokyo, Japan.

出版信息

PLoS Genet. 2017 Dec 21;13(12):e1007123. doi: 10.1371/journal.pgen.1007123. eCollection 2017 Dec.

Abstract

The heavily methylated vertebrate genomes are punctuated by stretches of poorly methylated DNA sequences that usually mark gene regulatory regions. It is known that the methylation state of these regions confers transcriptional control over their associated genes. Given its governance on the transcriptome, cellular functions and identity, genome-wide DNA methylation pattern is tightly regulated and evidently predefined. However, how is the methylation pattern determined in vivo remains enigmatic. Based on in silico and in vitro evidence, recent studies proposed that the regional hypomethylated state is primarily determined by local DNA sequence, e.g., high CpG density and presence of specific transcription factor binding sites. Nonetheless, the dependency of DNA methylation on nucleotide sequence has not been carefully validated in vertebrates in vivo. Herein, with the use of medaka (Oryzias latipes) as a model, the sequence dependency of DNA methylation was intensively tested in vivo. Our statistical modeling confirmed the strong statistical association between nucleotide sequence pattern and methylation state in the medaka genome. However, by manipulating the methylation state of a number of genomic sequences and reintegrating them into medaka embryos, we demonstrated that artificially conferred DNA methylation states were predominantly and robustly maintained in vivo, regardless of their sequences and endogenous states. This feature was also observed in the medaka transgene that had passed across generations. Thus, despite the observed statistical association, nucleotide sequence was unable to autonomously determine its own methylation state in medaka in vivo. Our results apparently argue against the notion of the governance on the DNA methylation by nucleotide sequence, but instead suggest the involvement of other epigenetic factors in defining and maintaining the DNA methylation landscape. Further investigation in other vertebrate models in vivo will be needed for the generalization of our observations made in medaka.

摘要

高度甲基化的脊椎动物基因组中穿插着一些甲基化程度较低的DNA序列片段,这些片段通常标记着基因调控区域。已知这些区域的甲基化状态赋予了对其相关基因的转录控制。鉴于其对转录组、细胞功能和特性的调控作用,全基因组DNA甲基化模式受到严格调控且显然是预先确定的。然而,甲基化模式在体内是如何确定的仍然是个谜。基于计算机模拟和体外实验证据,最近的研究提出区域低甲基化状态主要由局部DNA序列决定,例如高CpG密度和特定转录因子结合位点的存在。尽管如此,DNA甲基化对核苷酸序列的依赖性在脊椎动物体内尚未得到仔细验证。在此,我们以青鳉(Oryzias latipes)为模型,在体内对DNA甲基化的序列依赖性进行了深入测试。我们的统计模型证实了青鳉基因组中核苷酸序列模式与甲基化状态之间存在强烈的统计关联。然而,通过操纵一些基因组序列的甲基化状态并将它们重新整合到青鳉胚胎中,我们证明了人为赋予的DNA甲基化状态在体内主要且稳定地得以维持,无论其序列和内源状态如何。在跨代的青鳉转基因中也观察到了这一特征。因此,尽管观察到了统计关联,但核苷酸序列在青鳉体内无法自主决定其自身的甲基化状态。我们的结果显然与核苷酸序列决定DNA甲基化的观点相悖,反而表明其他表观遗传因素参与了DNA甲基化格局的定义和维持。为了将我们在青鳉中的观察结果推广,还需要在其他脊椎动物模型中进行进一步的体内研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dcdc/5755920/c85abbf70d2f/pgen.1007123.g001.jpg

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