Arabidopsis histone acetyltransferase complex coordinates cytoplasmic histone acetylation and nuclear chromatin accessibility

Conserved type B histone acetyltransferases are recognized for their role in acetylating newly synthesized histones in the cytoplasm of eukaryotes. However, their involvement in regulating chromatin within the nucleus remains unclear. Our study shows that the <i>Arabidopsis thaliana</i> type B histone acetyltransferase HAG2 interacts with the histone chaperones MSI2, MSI3, and NASP, as well as the histones H3 and H4, forming a complex in both the cytoplasm and the nucleus. Within this complex, HAG2 and MSI2/3 constitute a histone acetylation module essential for acetylating histone H4 in the cytoplasm. Furthermore, this module works together with NASP to regulate histone acetylation, chromatin accessibility, and gene transcription in the nucleus. This complex enhances chromatin accessibility near transcription start sites while reducing accessibility near transcription termination sites. Our findings reveal a distinct role for the <i>Arabidopsis</i> type B histone acetyltransferase in the nucleus, shedding light on the coordination between cytoplasmic histone acetylation and nuclear chromatin regulation in plants.

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Publication Details

Journal
Science Advances
Published
2024-12-04
DOI
https://doi.org/10.1126/sciadv.adp1840
Citations
9
Primary Topic
Plant Molecular Biology Research
Type
article
Field-Weighted Citation Impact
5.40
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article

Arabidopsis histone acetyltransferase complex coordinates cytoplasmic histone acetylation and nuclear chromatin accessibility

Yin‐Na Su, Xin‐Jian He, She Chen, Dan‐Yang Yuan et al.
9 citations
Science Advances
Plant Molecular Biology Research
5.40
article

Arabidopsis histone acetyltransferase complex coordinates cytoplasmic histone acetylation and nuclear chromatin accessibility

Yin‐Na Su, Xin‐Jian He, She Chen, Dan‐Yang Yuan, Chan‐Juan Wu, Zhenzhen Liu, Xin Xu, Lianmei Tan, Lin Li
article en
9 citations

Abstract

Conserved type B histone acetyltransferases are recognized for their role in acetylating newly synthesized histones in the cytoplasm of eukaryotes. However, their involvement in regulating chromatin within the nucleus remains unclear. Our study shows that the <i>Arabidopsis thaliana</i> type B histone acetyltransferase HAG2 interacts with the histone chaperones MSI2, MSI3, and NASP, as well as the histones H3 and H4, forming a complex in both the cytoplasm and the nucleus. Within this complex, HAG2 and MSI2/3 constitute a histone acetylation module essential for acetylating histone H4 in the cytoplasm. Furthermore, this module works together with NASP to regulate histone acetylation, chromatin accessibility, and gene transcription in the nucleus. This complex enhances chromatin accessibility near transcription start sites while reducing accessibility near transcription termination sites. Our findings reveal a distinct role for the <i>Arabidopsis</i> type B histone acetyltransferase in the nucleus, shedding light on the coordination between cytoplasmic histone acetylation and nuclear chromatin regulation in plants.

Science AdvancesVol. 10(49)
Southwest University of Science and Technology (CN), Beijing Normal University (CN), National Institute of Biological Sciences, Beijing (CN), Tsinghua University (CN)
Openalex Percentile: Top 5%
Plant Molecular Biology Research
5.40
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