Abstract

Chromatin organization is essential for coordinated gene expression, genome stability, and inheritance of epigenetic information. The main components involved in chromatin assembly are specific complexes such as Chromatin Assembly Factor 1 (CAF-1) and Histone Regulator (HIR), which deposit histones in a DNA synthesis-dependent or -independent manner, respectively. Here, we characterize the role of the plant orthologs Histone Regulator A (HIRA), Ubinuclein (UBN) and Calcineurin Binding protein 1 (CABIN1), which constitute the HIR complex. Arabidopsis loss-of-function mutants for the various subunits of the complex are viable, but hira mutants show reduced fertility. We show that loss of HIRA reduces extractable histone H3 protein levels and decreases nucleosome occupancy at both actively transcribed genes and heterochromatic regions. Concomitantly, HIRA contributes to maintenance of silencing of pericentromeric repeats and certain transposons. A genetic analysis based on crosses between mutants deficient in subunits of the CAF-1 and HIR complexes showed that simultaneous loss of both the CAF-1 and HIR histone H3 chaperone complexes severely affects plant survival, growth and reproductive development. Our results suggest that HIRA partially rescues impaired histone deposition in fas mutants to preserve nucleosome occupancy, implying plasticity in histone variant interaction and deposition.Significance StatementThis study describes the role of the evolutionary conserved histone chaperone complex HISTONE REGULATOR (HIR) in gene expression and plant development. Our results suggest that the HIR complex partially rescues impaired histone deposition in mutants lacking the CHROMATIN ASSEMBLY FACTOR 1 complex to sustain nucleosome occupancy.

Keywords

Arabidopsis; chaperone; histone; nucleosome; transcriptional silencing

Published in

Plant Journal
2015, Volume: 81, number: 5, pages: 707-722

UKÄ Subject classification

Genetics and Breeding


Publication identifier

DOI: https://doi.org/10.1111/tpj.12758

Permanent link to this page (URI)

https://res.slu.se/id/publ/84690