Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis. / Zhong, Zhenhui; Wang, Yafei; Wang, Ming; Yang, Fan; Thomas, Quentin Angelo; Xue, Yan; Zhang, Yaxin; Liu, Wanlu; Jami-Alahmadi, Yasaman; Xu, Linhao; Feng, Suhua; Marquardt, Sebastian; Wohlschlegel, James A; Ausin, Israel; Jacobsen, Steven E.

In: Nature Communications, Vol. 13, 6970, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Zhong, Z, Wang, Y, Wang, M, Yang, F, Thomas, QA, Xue, Y, Zhang, Y, Liu, W, Jami-Alahmadi, Y, Xu, L, Feng, S, Marquardt, S, Wohlschlegel, JA, Ausin, I & Jacobsen, SE 2022, 'Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis', Nature Communications, vol. 13, 6970. https://doi.org/10.1038/s41467-022-34648-0

APA

Zhong, Z., Wang, Y., Wang, M., Yang, F., Thomas, Q. A., Xue, Y., Zhang, Y., Liu, W., Jami-Alahmadi, Y., Xu, L., Feng, S., Marquardt, S., Wohlschlegel, J. A., Ausin, I., & Jacobsen, S. E. (2022). Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis. Nature Communications, 13, [6970]. https://doi.org/10.1038/s41467-022-34648-0

Vancouver

Zhong Z, Wang Y, Wang M, Yang F, Thomas QA, Xue Y et al. Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis. Nature Communications. 2022;13. 6970. https://doi.org/10.1038/s41467-022-34648-0

Author

Zhong, Zhenhui ; Wang, Yafei ; Wang, Ming ; Yang, Fan ; Thomas, Quentin Angelo ; Xue, Yan ; Zhang, Yaxin ; Liu, Wanlu ; Jami-Alahmadi, Yasaman ; Xu, Linhao ; Feng, Suhua ; Marquardt, Sebastian ; Wohlschlegel, James A ; Ausin, Israel ; Jacobsen, Steven E. / Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis. In: Nature Communications. 2022 ; Vol. 13.

Bibtex

@article{4827c86c26d54f0998a74996cd8bc468,
title = "Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis",
abstract = "Histone chaperones and chromatin remodelers control nucleosome dynamics, which are essential for transcription, replication, and DNA repair. The histone chaperone Anti-Silencing Factor 1 (ASF1) plays a central role in facilitating CAF-1-mediated replication-dependent H3.1 deposition and HIRA-mediated replication-independent H3.3 deposition in yeast and metazoans. Whether ASF1 function is evolutionarily conserved in plants is unknown. Here, we show that Arabidopsis ASF1 proteins display a preference for the HIRA complex. Simultaneous mutation of both Arabidopsis ASF1 genes caused a decrease in chromatin density and ectopic H3.1 occupancy at loci typically enriched with H3.3. Genetic, transcriptomic, and proteomic data indicate that ASF1 proteins strongly prefers the HIRA complex over CAF-1. asf1 mutants also displayed an increase in spurious Pol II transcriptional initiation and showed defects in the maintenance of gene body CG DNA methylation and in the distribution of histone modifications. Furthermore, ectopic targeting of ASF1 caused excessive histone deposition, less accessible chromatin, and gene silencing. These findings reveal the importance of ASF1-mediated histone deposition for proper epigenetic regulation of the genome.",
keywords = "Arabidopsis/genetics, Cell Cycle Proteins/metabolism, Chromatin/genetics, Chromatin Assembly Factor-1/genetics, Epigenesis, Genetic, Histone Chaperones/genetics, Histones/genetics, Molecular Chaperones/genetics, Proteomics, Arabidopsis Proteins",
author = "Zhenhui Zhong and Yafei Wang and Ming Wang and Fan Yang and Thomas, {Quentin Angelo} and Yan Xue and Yaxin Zhang and Wanlu Liu and Yasaman Jami-Alahmadi and Linhao Xu and Suhua Feng and Sebastian Marquardt and Wohlschlegel, {James A} and Israel Ausin and Jacobsen, {Steven E}",
note = "{\textcopyright} 2022. The Author(s).",
year = "2022",
doi = "10.1038/s41467-022-34648-0",
language = "English",
volume = "13",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Histone chaperone ASF1 mediates H3.3-H4 deposition in Arabidopsis

AU - Zhong, Zhenhui

AU - Wang, Yafei

AU - Wang, Ming

AU - Yang, Fan

AU - Thomas, Quentin Angelo

AU - Xue, Yan

AU - Zhang, Yaxin

AU - Liu, Wanlu

AU - Jami-Alahmadi, Yasaman

AU - Xu, Linhao

AU - Feng, Suhua

AU - Marquardt, Sebastian

AU - Wohlschlegel, James A

AU - Ausin, Israel

AU - Jacobsen, Steven E

N1 - © 2022. The Author(s).

PY - 2022

Y1 - 2022

N2 - Histone chaperones and chromatin remodelers control nucleosome dynamics, which are essential for transcription, replication, and DNA repair. The histone chaperone Anti-Silencing Factor 1 (ASF1) plays a central role in facilitating CAF-1-mediated replication-dependent H3.1 deposition and HIRA-mediated replication-independent H3.3 deposition in yeast and metazoans. Whether ASF1 function is evolutionarily conserved in plants is unknown. Here, we show that Arabidopsis ASF1 proteins display a preference for the HIRA complex. Simultaneous mutation of both Arabidopsis ASF1 genes caused a decrease in chromatin density and ectopic H3.1 occupancy at loci typically enriched with H3.3. Genetic, transcriptomic, and proteomic data indicate that ASF1 proteins strongly prefers the HIRA complex over CAF-1. asf1 mutants also displayed an increase in spurious Pol II transcriptional initiation and showed defects in the maintenance of gene body CG DNA methylation and in the distribution of histone modifications. Furthermore, ectopic targeting of ASF1 caused excessive histone deposition, less accessible chromatin, and gene silencing. These findings reveal the importance of ASF1-mediated histone deposition for proper epigenetic regulation of the genome.

AB - Histone chaperones and chromatin remodelers control nucleosome dynamics, which are essential for transcription, replication, and DNA repair. The histone chaperone Anti-Silencing Factor 1 (ASF1) plays a central role in facilitating CAF-1-mediated replication-dependent H3.1 deposition and HIRA-mediated replication-independent H3.3 deposition in yeast and metazoans. Whether ASF1 function is evolutionarily conserved in plants is unknown. Here, we show that Arabidopsis ASF1 proteins display a preference for the HIRA complex. Simultaneous mutation of both Arabidopsis ASF1 genes caused a decrease in chromatin density and ectopic H3.1 occupancy at loci typically enriched with H3.3. Genetic, transcriptomic, and proteomic data indicate that ASF1 proteins strongly prefers the HIRA complex over CAF-1. asf1 mutants also displayed an increase in spurious Pol II transcriptional initiation and showed defects in the maintenance of gene body CG DNA methylation and in the distribution of histone modifications. Furthermore, ectopic targeting of ASF1 caused excessive histone deposition, less accessible chromatin, and gene silencing. These findings reveal the importance of ASF1-mediated histone deposition for proper epigenetic regulation of the genome.

KW - Arabidopsis/genetics

KW - Cell Cycle Proteins/metabolism

KW - Chromatin/genetics

KW - Chromatin Assembly Factor-1/genetics

KW - Epigenesis, Genetic

KW - Histone Chaperones/genetics

KW - Histones/genetics

KW - Molecular Chaperones/genetics

KW - Proteomics

KW - Arabidopsis Proteins

U2 - 10.1038/s41467-022-34648-0

DO - 10.1038/s41467-022-34648-0

M3 - Journal article

C2 - 36379930

VL - 13

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

M1 - 6970

ER -

ID: 327942140