Abstract

BackgroundPolycomb Repressive Complexes 2 (PRC2) are multi-protein chromatin modifiers that are evolutionarily conserved among eukaryotes and play key roles in the regulation of gene expression, notably through the trimethylation of lysine 27 of histone H3 (H3K27me3). Although PRC2-mediated gene regulation has been studied in many organisms, few studies have explored in depth the evolutionary conservation of PRC2 targets.ResultsHere, we compare the H3K27me3 epigenomic profiles for the two closely related species Arabidopsis thaliana and Arabidopsis lyrata and the more distant species Arabis alpina, three Brassicaceae that diverged from each other within the past 24 million years.Using a robust set of gene orthologs present in the three species, we identify two classes of evolutionarily conserved PRC2 targets, which are characterized by either developmentally plastic or developmentally constrained H3K27me3 marking across species. Constrained H3K27me3 marking is associated with higher conservation of promoter sequence information content and higher nucleosome occupancy compared to plastic H3K27me3 marking. Moreover, gene orthologs with constrained H3K27me3 marking exhibit a higher degree of tissue specificity and tend to be involved in developmental functions, whereas gene orthologs with plastic H3K27me3 marking preferentially encode proteins associated with metabolism and stress responses. In addition, gene orthologs with constrained H3K27me3 marking are the predominant contributors to higher-order chromosome organization.ConclusionsOur findings indicate that developmentally plastic and constrained H3K27me3 marking define two evolutionarily conserved modes of PRC2-mediated gene regulation that are associated with distinct selective pressures operating at multiple scales, from DNA sequence to gene function and chromosome architecture.

Highlights

  • Polycomb Repressive Complexes 2 (PRC2) are multi-protein chromatin modifiers that are evolutionarily conserved among eukaryotes and play key roles in the regulation of gene expression, notably through the trimethylation of lysine 27 of histone H3 (H3K27me3)

  • Initial work based on the genome sequence of Arabidopsis thaliana (Ath), Arabidopsis lyrata (Aly), Capsella rubella, Brassica rapa, and Thellungiella parvula led to the reconstruction of the ancestral Brassicaceae karyotype with 30,968 protogenes [16]

  • Gene orthologs with constrained H3K27me3 marking are important contributors to long-range intra-chromosomal interactions Given the implication of H3K27me3 domains in the three-dimensional (3D) conformation of chromosomes in many eukaryotes including plants [25,26,27,28], we investigated whether PRC2 targets with plastic and constrained marking could be distinguished by their chromosomal position or their implication in the spatial organization of the genome

Read more

Summary

Introduction

Polycomb Repressive Complexes 2 (PRC2) are multi-protein chromatin modifiers that are evolutionarily conserved among eukaryotes and play key roles in the regulation of gene expression, notably through the trimethylation of lysine 27 of histone H3 (H3K27me). In the flowering plant Arabidopsis thaliana, PRC2-mediated regulation of gene expression is involved in key developmental decisions throughout the life cycle, including postembryonic growth following seed germination and flowering [4]. In contrast to D. melanogaster, which contains a single E(z) and a single PRC2 holoenzyme, there are three E(z)-like proteins in Arabidopsis thaliana, called MEDEA (MEA), SWINGER (SWN), and CURLY LEAF (CLF). SWN and CLF are likely responsible for all H3K27me marking outside of the endosperm, and this marking affects around 30% of Arabidopsis thaliana genes in total, based on epigenomic maps obtained for multiple developmental stages and tissues [5]. In agreement with the critical role of PRC2 in orchestrating plant development and growth, H3K27me3-marked genes are notably enriched in transcription factors (TFs) as well as in components of hormone signaling [6,7,8,9]

Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.