胚エピゲノムの自己組織化の物理原理を解明(How the embryonal epigenome organizes itself)

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2026-04-29 ミュンヘン大学(LMU)

ミュンヘン大学の研究チームは、胚発生初期においてエピゲノムがどのように自己組織化するかを解明した。DNA配列そのものではなく、化学修飾やクロマチン構造といったエピゲノム情報が、時間とともに秩序だったパターンを形成し、遺伝子発現の制御を担うことが示された。特に、細胞分化の初期段階でエピゲノムが自律的に再編成される仕組みが明らかになり、発生過程の理解を深める成果である。この知見は、発生異常や疾患の原因解明、再生医療への応用にもつながる可能性がある。

<関連情報>

胚性エピゲノム形成におけるスケーリングと自己相似性 Scaling and self-similarity in the formation of the embryonic epigenome

Fabrizio Olmeda,Tim Lohoff,Ioannis Kafetzopoulos,Stephen J. Clark,Laura Benson,Fatima Santos,Felix Krueger,Simon Walker,Wolf Reik & Steffen Rulands
Nature Physics  Published:29 April 2026
DOI:https://doi.org/10.1038/s41567-026-03263-x

胚エピゲノムの自己組織化の物理原理を解明(How the embryonal epigenome organizes itself)

Abstract

The development of complex tissues relies on the precise assignment of cell identity. At the molecular scale, this process depends on the deposition of epigenetic modifications—such as methylation—that are regulated by complex biochemical networks and occur at specific regions on the DNA and chromatin. Here we show that despite the complexity of epigenetic regulation, dynamical scaling and self-similarity of DNA methylation marks emerge in embryonic development. Drawing on single-cell multi-omics experiments, super-resolution microscopy and statistical physics, we demonstrate that these phenomena originate in dynamical feedback between DNA methylation and the formation of nanoscale dynamic chromatin aggregates. These nanoscale processes lead to genome-wide increase in DNA methylation marks following a power law and self-similar correlation functions. Using this framework, we identify methylation patterns that precede gene expression changes in embryonic symmetry breaking. Our work identifies linear sequencing measurements as a laboratory to study mesoscopic biophysical processes in vivo.

細胞遺伝子工学
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