靶向染色质编辑揭示的模拟表观遗传记忆。

IF 11.1 Q1 CELL BIOLOGY
Sebastian Palacios, Simone Bruno, Ron Weiss, Elia Salibi, Isabella Goodchild-Michelman, Andrew Kane, Katherine Ilia, Domitilla Del Vecchio
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引用次数: 0

摘要

细胞通过染色质修饰来存储信息,这种修饰在细胞分裂过程中持续存在,并可以在几代人的时间内保持基因表达沉默。然而,这些修饰如何维持其他基因表达状态仍不清楚。这项研究表明,随着时间的推移,染色质修饰可以维持大范围的基因表达水平,从而揭示类似的表观遗传记忆。通过设计基因组报告因子和表观遗传效应因子,我们跟踪了靶向干扰染色质状态后的基因表达动态。我们发现不同程度的DNA甲基化导致相应的、持续的基因表达水平。反过来,改变DNA甲基化等级会导致基因表达记忆的永久性丧失。与实验结果一致,我们的染色质修饰模型表明,当DNA甲基化和抑制性组蛋白修饰之间缺乏正反馈时,模拟记忆就会出现。这一发现将导致对表观遗传记忆的更深层次的理解,并为合成生物学提供新的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analog epigenetic memory revealed by targeted chromatin editing.

Cells store information by means of chromatin modifications that persist through cell divisions and can hold gene expression silenced over generations. However, how these modifications may maintain other gene expression states has remained unclear. This study shows that chromatin modifications can maintain a wide range of gene expression levels over time, thus uncovering analog epigenetic memory. By engineering a genomic reporter and epigenetic effectors, we tracked the gene expression dynamics following targeted perturbations to the chromatin state. We found that distinct grades of DNA methylation led to corresponding, persistent gene expression levels. Altering the DNA methylation grade, in turn, resulted in permanent loss of gene expression memory. Consistent with experiments, our chromatin modification model indicates that analog memory arises when the positive feedback between DNA methylation and repressive histone modifications is lacking. This discovery will lead to a deeper understanding of epigenetic memory and to new tools for synthetic biology.

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CiteScore
7.10
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