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Nature · 2025

An integrated view of the structure and function of the human 4D nucleome.

СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
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Dekker Job, Oksuz Betul Akgol, Zhang Yang, Wang Ye, Minsk Miriam K, Kuang Shuzhen, Yang Liyan, Gibcus Johan H, Krietenstein Nils, Rando Oliver J, Xu Jie, Janssens Derek H, Henikoff Steven, Kukalev Alexander, Andréa Willemin, Winick-Ng Warren, Kempfer Rieke, Pombo Ana, Yu Miao, Kumar Pradeep, Zhang Liguo, Belmont Andrew S, Sasaki Takayo, van Schaik Tom, Brueckner Laura, Peric-Hupkes Daan, van Steensel Bas, Wang Ping, Chai Haoxi, Kim Minji, Ruan Yijun, Zhang Ran, Quinodoz Sofia A, Bhat Prashant, Guttman Mitchell, Zhao Wenxin, Chien Shu, Liu Yuan, Venev Sergey V, Plewczynski Dariusz, Azcarate Ibai Irastorza, Szabó Dominik, Thieme Christoph J, Szczepińska Teresa, Chiliński Mateusz, Sengupta Kaustav, Conte Mattia, Esposito Andrea, Abraham Alex, Zhang Ruochi, Wang Yuchuan, Wen Xingzhao, Wu Qiuyang, Yang Yang, Liu Jie, Boninsegna Lorenzo, Yildirim Asli, Zhan Yuxiang, Chiariello Andrea Maria, Bianco Simona, Lee Lindsay, Hu Ming, Li Yun, Barnett R Jordan, Cook Ashley L, Emerson Daniel J, Marchal Claire, Zhao Peiyao, Park Peter J, Alver Burak H, Schroeder Andrew J, Navelkar Rahi, Bakker Clara, Ronchetti William, Ehmsen Shannon, Veit Alexander D, Gehlenborg Nils, Wang Ting, Li Daofeng, Wang Xiaotao, Nicodemi Mario, Ren Bing, Zhong Sheng, Phillips-Cremins Jennifer E, Gilbert David M, Pollard Katherine S, Alber Frank, Ma Jian, Noble William S, Yue Feng

Аннотация

The dynamic three-dimensional (3D) organization of the human genome (the 4D nucleome) is linked to genome function. Here we describe efforts by the 4D Nucleome Project1 to map and analyse the 4D nucleome in widely used H1 human embryonic stem cells and immortalized fibroblasts (HFFc6). We produced and integrated diverse genomic datasets of the 4D nucleome, each contributing unique observations, which enabled us to assemble extensive catalogues of more than 140,000 looping interactions per cell type, to generate detailed classifications and annotations of chromosomal domain types and their subnuclear positions, and to obtain single-cell 3D models of the nuclear environment of all genes including their long-range interactions with distal elements. Through extensive benchmarking, we describe the unique strengths of different genomic assays for studying the 4D nucleome, providing guidelines for future studies. Three-dimensional models of population-based and individual cell-to-cell variation in genome structure showed connections between chromosome folding, nuclear organization, chromatin looping, gene transcription and DNA replication. Finally, we demonstrate the use of computational methods to predict genome folding from DNA sequence, which will facilitate the discovery of potential effects of genetic variants, including variants associated with disease, on genome structure and function.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты