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Recent advances in chromosome capture techniques unraveling 3D genome architecture in germ cells, health, and disease

Author(s)
Pandupuspitasari, Nuruliarizki S.; Khan, Faheem A.; Huang, Chunjie; Ali, Azhar; Yousaf, Muhammad R.; Shakeel, Farwa; Putri, Ezi M.; Negara, Windu; Muktiani, Anis; Prasetiyono, Bambang W. H. E.; Kustiawan, Limbang; Wahyuni, Dimar S.; ... Show more Show less
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.

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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
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Abstract
Abstract In eukaryotes, the genome does not emerge in a specific shape but rather as a hierarchial bundle within the nucleus. This multifaceted genome organization consists of multiresolution cellular structures, such as chromosome territories, compartments, and topologically associating domains, which are frequently defined by architecture, design proteins including CTCF and cohesin, and chromatin loops. This review briefly discusses the advances in understanding the basic rules of control, chromatin folding, and functional areas in early embryogenesis. With the use of chromosome capture techniques, the latest advancements in technologies for visualizing chromatin interactions come close to revealing 3D genome formation frameworks with incredible detail throughout all genomic levels, including at single-cell resolution. The possibility of detecting variations in chromatin architecture might open up new opportunities for disease diagnosis and prevention, infertility treatments, therapeutic approaches, desired exploration, and many other application scenarios.
Date issued
2023-06-29
URI
https://hdl.handle.net/1721.1/152309
Department
Massachusetts Institute of Technology. Department of Biological Engineering
Publisher
Springer Berlin Heidelberg
Citation
Functional & Integrative Genomics. 2023 Jun 29;23(3):214
Version: Author's final manuscript

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