TY - JOUR
T1 - Hmo1 Protein Affects the Nucleosome Structure and Supports the Nucleosome Reorganization Activity of Yeast FACT
AU - Malinina, Daria K.
AU - Sivkina, Anastasiia L.
AU - Korovina, Anna N.
AU - McCullough, Laura L.
AU - Formosa, Tim
AU - Kirpichnikov, Mikhail P.
AU - Studitsky, Vasily M.
AU - Feofanov, Alexey V.
N1 - Publisher Copyright:
© 2022 by the authors.
PY - 2022/8/20
Y1 - 2022/8/20
N2 - 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.
AB - 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.
KW - EMSA
KW - FACT
KW - H1 histone
KW - high mobility group B protein
KW - Hmo1
KW - nucleosome
KW - spFRET
UR - http://www.scopus.com/inward/record.url?scp=85139779460&partnerID=8YFLogxK
U2 - 10.3390/cells11192931
DO - 10.3390/cells11192931
M3 - Article
C2 - 36230893
AN - SCOPUS:85139779460
SN - 2073-4409
VL - 11
JO - Cells
JF - Cells
IS - 19
M1 - 2931
ER -