HDA6 dependent chromatin deacetylation orchestrates mRNA polyadenylation

  1. Qingshun Quinn Li4,5
  1. 1 Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystems, Xiamen University;
  2. 2 Institute of Plant Biology, National Taiwan University;
  3. 3 Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystems, Xiamen University,;
  4. 4 Western University of Health Sciences
  • * Corresponding author; email: qqli{at}westernu.edu
  • Abstract

    Eukaryotic histone deacetylation, critical for maintaining nucleosome structure and regulating gene expression, is mediated by histone deacetylases (HDACs). While nucleosomes have been reported to regulate mRNA polyadenylation in humans, the role of HDACs in regulating polyadenylation has not been uncovered. Taking the advantage of phenotypic studies on Arabidopsis, HDA6 (one of HDACs) was found to be a critical part of many biological processes. Here, we report that HDA6 affects mRNA polyadenylation of Arabidopsis. Poly(A) sites of upregulated transcripts are closer to the histone acetylation peaks in hda6 compared to the wild-type Col-0. HDA6 is required for the deacetylation of histones around DNA on nucleosomes, which solely coincides with up-regulated or uniquely presented poly(A) sites in hda6. Furthermore, defective HDA6 results in an over-representation of the canonical poly(A) signal (AAUAAA) usages. Chromatins for generating AAUAAA-type transcripts have a comparatively low H3K9K14ac around poly(A) sites when compared to other non-canonical poly(A) signal containing transcripts. These results indicate that HDA6 regulates polyadenylation in a histone deacetylation dependent manner in Arabidopsis.

    • Received July 29, 2019.
    • Accepted July 28, 2020.

    This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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    1. Genome Res. gr.255232.119 Published by Cold Spring Harbor Laboratory Press

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