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Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus

Chromatin compaction and regulation are essential processes for the normal function of all organisms, yet knowledge on how archaeal chromosomes are packed into higher-order structures inside the cell remains elusive. In this study, we investigated the role of archaeal architectural proteins Alba and...

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Autores principales: Cajili, Marc Kenneth M., Prieto, Eloise I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030869/
https://www.ncbi.nlm.nih.gov/pubmed/35454068
http://dx.doi.org/10.3390/biom12040481
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author Cajili, Marc Kenneth M.
Prieto, Eloise I.
author_facet Cajili, Marc Kenneth M.
Prieto, Eloise I.
author_sort Cajili, Marc Kenneth M.
collection PubMed
description Chromatin compaction and regulation are essential processes for the normal function of all organisms, yet knowledge on how archaeal chromosomes are packed into higher-order structures inside the cell remains elusive. In this study, we investigated the role of archaeal architectural proteins Alba and Cren7 in chromatin folding and dynamics. Atomic force microscopy revealed that Sulfolobus solfataricus chromatin is composed of 28 nm fibers and 60 nm globular structures. In vitro reconstitution showed that Alba can mediate the formation of folded DNA structures in a concentration-dependent manner. Notably, it was demonstrated that Alba on its own can form higher-order structures with DNA. Meanwhile, Cren7 was observed to affect the formation of Alba-mediated higher-order chromatin structures. Overall, the results suggest an interplay between Alba and Cren7 in regulating chromatin compaction in archaea.
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spelling pubmed-90308692022-04-23 Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus Cajili, Marc Kenneth M. Prieto, Eloise I. Biomolecules Article Chromatin compaction and regulation are essential processes for the normal function of all organisms, yet knowledge on how archaeal chromosomes are packed into higher-order structures inside the cell remains elusive. In this study, we investigated the role of archaeal architectural proteins Alba and Cren7 in chromatin folding and dynamics. Atomic force microscopy revealed that Sulfolobus solfataricus chromatin is composed of 28 nm fibers and 60 nm globular structures. In vitro reconstitution showed that Alba can mediate the formation of folded DNA structures in a concentration-dependent manner. Notably, it was demonstrated that Alba on its own can form higher-order structures with DNA. Meanwhile, Cren7 was observed to affect the formation of Alba-mediated higher-order chromatin structures. Overall, the results suggest an interplay between Alba and Cren7 in regulating chromatin compaction in archaea. MDPI 2022-03-22 /pmc/articles/PMC9030869/ /pubmed/35454068 http://dx.doi.org/10.3390/biom12040481 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cajili, Marc Kenneth M.
Prieto, Eloise I.
Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus
title Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus
title_full Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus
title_fullStr Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus
title_full_unstemmed Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus
title_short Interplay between Alba and Cren7 Regulates Chromatin Compaction in Sulfolobus solfataricus
title_sort interplay between alba and cren7 regulates chromatin compaction in sulfolobus solfataricus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030869/
https://www.ncbi.nlm.nih.gov/pubmed/35454068
http://dx.doi.org/10.3390/biom12040481
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