ゲノム構造をかつてない精度でマッピング(Oxford Scientists Capture Genome’s Structure in Unprecedented Detail)

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2025-11-06 オックスフォード大学

オックスフォード大学ラドクリフ医学部の研究チームは、DNAが細胞内でどのように折りたたまれ、遺伝子のON/OFFを制御しているかを塩基対レベルで可視化する新技術「MCC ultra」を開発した。これにより、遺伝子発現を決定する物理的構造を前例のない詳細さで描き出すことに成功。90%以上の疾患関連変異が遺伝子そのものではなく制御領域に存在することから、この成果は病気発症機構や創薬研究に新たな道を開く。DNA折りたたみ構造のシミュレーションにはケンブリッジ大学も協力し、電磁的相互作用によって遺伝子活性「島」が形成される新モデルを提案した。成果はCell誌に掲載。

<関連情報>

塩基対解像度でのクロマチン構造のマッピングにより、シス調節要素相互作用の統一モデルが明らかになった Mapping chromatin structure at base-pair resolution unveils a unified model of cis-regulatory element interactions

Hangpeng Li, James L.T. Dalgleish, George Lister, Maria Julia Maristany, Jan Huertas, Ana M. Dopico-Fernandez, Joseph C. Hamley, Nicholas Denny, Gianna Bloye, Weijiao Zhang, Lance Hentges, Roman Doll, Ye Wei, Michela Maresca, Emilia Dimitrova, Lior Pytowski, Edward A.J. Tunnacliffe, Mira Kassouf, Doug Higgs, Elzo de Wit, Robert J. Klose, Lothar Schermelleh, Rosana Collepardo-Guevara, Thomas A. Milne, James O.J. Davies
Cell  Available online: 5 November 2025
DOI:https://doi.org/10.1016/j.cell.2025.10.013

Graphical abstract

ゲノム構造をかつてない精度でマッピング(Oxford Scientists Capture Genome’s Structure in Unprecedented Detail)

Highlights

  • Base-pair resolution MCCu reveals complex structures within cis-regulatory elements
  • Mediator complex components largely contribute to the fine-scale structure of promoters
  • Long-range contacts are driven by transcription factor-mediated nucleosome depletion
  • Chromatin structure is likely coordinated by the biophysical properties of nucleosomes

Summary

Chromatin structure is a key determinant of gene expression in eukaryotes, but it has not been possible to define the structure of cis-regulatory elements at the scale of the proteins that bind them. Here, we generate multidimensional chromosome conformation capture (3C) maps at base-pair resolution using Micro Capture-C ultra (MCCu). This can resolve contacts between individual transcription factor motifs within cis-regulatory elements. Using degron systems, we show that removal of Mediator complex components alters fine-scale promoter structure and that nucleosome depletion plays a key role in transcription factor-driven enhancer-promoter contacts. We observe that chromatin is partitioned into nanoscale domains by nucleosome-depleted regions. This structural conformation is reproduced by chemically specific coarse-grained molecular dynamics simulations of the physicochemical properties of chromatin. Combining MCCu with molecular dynamics simulations and super-resolution microscopy allows us to propose a unified model in which the biophysical properties of chromatin orchestrate contacts between cis-regulatory elements.

細胞遺伝子工学
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