Genome wide nucleosome landscape shapes 3D chromatin organization

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Genome wide nucleosome landscape shapes 3D chromatin organization. / Fouziya, Shah; Krietenstein, Nils; Mir, Ulfat Syed; Mieczkowski, Jakub; Khan, Masood A.; Baba, Aemon; Dar, Mohmmad Abaas; Altaf, Mohammad; Wani, Ajazul H.

In: Science Advances, Vol. 10, No. 23, eadn2955, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Fouziya, S, Krietenstein, N, Mir, US, Mieczkowski, J, Khan, MA, Baba, A, Dar, MA, Altaf, M & Wani, AH 2024, 'Genome wide nucleosome landscape shapes 3D chromatin organization', Science Advances, vol. 10, no. 23, eadn2955. https://doi.org/10.1126/sciadv.adn2955

APA

Fouziya, S., Krietenstein, N., Mir, U. S., Mieczkowski, J., Khan, M. A., Baba, A., Dar, M. A., Altaf, M., & Wani, A. H. (2024). Genome wide nucleosome landscape shapes 3D chromatin organization. Science Advances, 10(23), [eadn2955]. https://doi.org/10.1126/sciadv.adn2955

Vancouver

Fouziya S, Krietenstein N, Mir US, Mieczkowski J, Khan MA, Baba A et al. Genome wide nucleosome landscape shapes 3D chromatin organization. Science Advances. 2024;10(23). eadn2955. https://doi.org/10.1126/sciadv.adn2955

Author

Fouziya, Shah ; Krietenstein, Nils ; Mir, Ulfat Syed ; Mieczkowski, Jakub ; Khan, Masood A. ; Baba, Aemon ; Dar, Mohmmad Abaas ; Altaf, Mohammad ; Wani, Ajazul H. / Genome wide nucleosome landscape shapes 3D chromatin organization. In: Science Advances. 2024 ; Vol. 10, No. 23.

Bibtex

@article{698f6c76c72840d58d3863fa6c1177c2,
title = "Genome wide nucleosome landscape shapes 3D chromatin organization",
abstract = "The hierarchical chromatin organization begins with formation of nucleosomes, which fold into chromatin domains punctuated by boundaries and ultimately chromosomes. In a hierarchal organization, lower levels shape higher levels. However, the dependence of higher-order 3D chromatin organization on the nucleosome-level organization has not been studied in cells. We investigated the relationship between nucleosome-level organization and higher-order chromatin organization by perturbing nucleosomes across the genome by deleting Imitation SWItch (ISWI) and Chromodomain Helicase DNA-binding (CHD1) chromatin remodeling factors in budding yeast. We find that changes in nucleosome-level properties are accompanied by changes in 3D chromatin organization. Short-range chromatin contacts up to a few kilo–base pairs decrease, chromatin domains weaken, and boundary strength decreases. Boundary strength scales with accessibility and moderately with width of nucleosome-depleted region. Change in nucleosome positioning seems to alter the stiffness of chromatin, which can affect formation of chromatin contacts. Our results suggest a biomechanical “bottom-up” mechanism by which nucleosome distribution across genome shapes 3D chromatin organization.",
author = "Shah Fouziya and Nils Krietenstein and Mir, {Ulfat Syed} and Jakub Mieczkowski and Khan, {Masood A.} and Aemon Baba and Dar, {Mohmmad Abaas} and Mohammad Altaf and Wani, {Ajazul H.}",
note = "Publisher Copyright: Copyright {\textcopyright} 2024 The Authors, some rights reserved",
year = "2024",
doi = "10.1126/sciadv.adn2955",
language = "English",
volume = "10",
journal = "Science advances",
issn = "2375-2548",
publisher = "American Association for the Advancement of Science",
number = "23",

}

RIS

TY - JOUR

T1 - Genome wide nucleosome landscape shapes 3D chromatin organization

AU - Fouziya, Shah

AU - Krietenstein, Nils

AU - Mir, Ulfat Syed

AU - Mieczkowski, Jakub

AU - Khan, Masood A.

AU - Baba, Aemon

AU - Dar, Mohmmad Abaas

AU - Altaf, Mohammad

AU - Wani, Ajazul H.

N1 - Publisher Copyright: Copyright © 2024 The Authors, some rights reserved

PY - 2024

Y1 - 2024

N2 - The hierarchical chromatin organization begins with formation of nucleosomes, which fold into chromatin domains punctuated by boundaries and ultimately chromosomes. In a hierarchal organization, lower levels shape higher levels. However, the dependence of higher-order 3D chromatin organization on the nucleosome-level organization has not been studied in cells. We investigated the relationship between nucleosome-level organization and higher-order chromatin organization by perturbing nucleosomes across the genome by deleting Imitation SWItch (ISWI) and Chromodomain Helicase DNA-binding (CHD1) chromatin remodeling factors in budding yeast. We find that changes in nucleosome-level properties are accompanied by changes in 3D chromatin organization. Short-range chromatin contacts up to a few kilo–base pairs decrease, chromatin domains weaken, and boundary strength decreases. Boundary strength scales with accessibility and moderately with width of nucleosome-depleted region. Change in nucleosome positioning seems to alter the stiffness of chromatin, which can affect formation of chromatin contacts. Our results suggest a biomechanical “bottom-up” mechanism by which nucleosome distribution across genome shapes 3D chromatin organization.

AB - The hierarchical chromatin organization begins with formation of nucleosomes, which fold into chromatin domains punctuated by boundaries and ultimately chromosomes. In a hierarchal organization, lower levels shape higher levels. However, the dependence of higher-order 3D chromatin organization on the nucleosome-level organization has not been studied in cells. We investigated the relationship between nucleosome-level organization and higher-order chromatin organization by perturbing nucleosomes across the genome by deleting Imitation SWItch (ISWI) and Chromodomain Helicase DNA-binding (CHD1) chromatin remodeling factors in budding yeast. We find that changes in nucleosome-level properties are accompanied by changes in 3D chromatin organization. Short-range chromatin contacts up to a few kilo–base pairs decrease, chromatin domains weaken, and boundary strength decreases. Boundary strength scales with accessibility and moderately with width of nucleosome-depleted region. Change in nucleosome positioning seems to alter the stiffness of chromatin, which can affect formation of chromatin contacts. Our results suggest a biomechanical “bottom-up” mechanism by which nucleosome distribution across genome shapes 3D chromatin organization.

U2 - 10.1126/sciadv.adn2955

DO - 10.1126/sciadv.adn2955

M3 - Journal article

C2 - 38848364

AN - SCOPUS:85195533992

VL - 10

JO - Science advances

JF - Science advances

SN - 2375-2548

IS - 23

M1 - eadn2955

ER -

ID: 395391459