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Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT
Yeast Hmo1 is a high mobility group B (HMGB) protein that participates in the transcription of ribosomal protein genes and rDNA, and also stimulates the activities of some ATP-dependent remodelers. Hmo1 binds both DNA and nucleosomes and has been proposed to be a functional yeast analog of mammalian...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564320/ https://www.ncbi.nlm.nih.gov/pubmed/36230893 http://dx.doi.org/10.3390/cells11192931 |
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author | Malinina, Daria K. Sivkina, Anastasiia L. Korovina, Anna N. McCullough, Laura L. Formosa, Tim Kirpichnikov, Mikhail P. Studitsky, Vasily M. Feofanov, Alexey V. |
author_facet | Malinina, Daria K. Sivkina, Anastasiia L. Korovina, Anna N. McCullough, Laura L. Formosa, Tim Kirpichnikov, Mikhail P. Studitsky, Vasily M. Feofanov, Alexey V. |
author_sort | Malinina, Daria K. |
collection | PubMed |
description | Yeast Hmo1 is a high mobility group B (HMGB) protein that participates in the transcription of ribosomal protein genes and rDNA, and also stimulates the activities of some ATP-dependent remodelers. Hmo1 binds both DNA and nucleosomes and has been proposed to be a functional yeast analog of mammalian linker histones. We used EMSA and single particle Förster resonance energy transfer (spFRET) microscopy to characterize the effects of Hmo1 on nucleosomes alone and with the histone chaperone FACT. Hmo1 induced a significant increase in the distance between the DNA gyres across the nucleosomal core, and also caused the separation of linker segments. This was opposite to the effect of the linker histone H1, which enhanced the proximity of linkers. Similar to Nhp6, another HMGB factor, Hmo1, was able to support large-scale, ATP-independent, reversible unfolding of nucleosomes by FACT in the spFRET assay and partially support FACT function in vivo. However, unlike Hmo1, Nhp6 alone does not affect nucleosome structure. These results suggest physiological roles for Hmo1 that are distinct from Nhp6 and possibly from other HMGB factors and linker histones, such as H1. |
format | Online Article Text |
id | pubmed-9564320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95643202022-10-15 Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT Malinina, Daria K. Sivkina, Anastasiia L. Korovina, Anna N. McCullough, Laura L. Formosa, Tim Kirpichnikov, Mikhail P. Studitsky, Vasily M. Feofanov, Alexey V. Cells Article Yeast Hmo1 is a high mobility group B (HMGB) protein that participates in the transcription of ribosomal protein genes and rDNA, and also stimulates the activities of some ATP-dependent remodelers. Hmo1 binds both DNA and nucleosomes and has been proposed to be a functional yeast analog of mammalian linker histones. We used EMSA and single particle Förster resonance energy transfer (spFRET) microscopy to characterize the effects of Hmo1 on nucleosomes alone and with the histone chaperone FACT. Hmo1 induced a significant increase in the distance between the DNA gyres across the nucleosomal core, and also caused the separation of linker segments. This was opposite to the effect of the linker histone H1, which enhanced the proximity of linkers. Similar to Nhp6, another HMGB factor, Hmo1, was able to support large-scale, ATP-independent, reversible unfolding of nucleosomes by FACT in the spFRET assay and partially support FACT function in vivo. However, unlike Hmo1, Nhp6 alone does not affect nucleosome structure. These results suggest physiological roles for Hmo1 that are distinct from Nhp6 and possibly from other HMGB factors and linker histones, such as H1. MDPI 2022-09-20 /pmc/articles/PMC9564320/ /pubmed/36230893 http://dx.doi.org/10.3390/cells11192931 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 Malinina, Daria K. Sivkina, Anastasiia L. Korovina, Anna N. McCullough, Laura L. Formosa, Tim Kirpichnikov, Mikhail P. Studitsky, Vasily M. Feofanov, Alexey V. Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT |
title | Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT |
title_full | Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT |
title_fullStr | Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT |
title_full_unstemmed | Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT |
title_short | Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT |
title_sort | hmo1 protein affects the nucleosome structure and supports the nucleosome reorganization activity of yeast fact |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564320/ https://www.ncbi.nlm.nih.gov/pubmed/36230893 http://dx.doi.org/10.3390/cells11192931 |
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