Abstract

BackgroundChromatin organizational and topological plasticity, and its functions in gene expression regulation, have been strongly revealed by the analysis of nucleolar dominance in hybrids and polyploids where one parental set of ribosomal RNA (rDNA) genes that are clustered in nucleolar organizing regions (NORs), is rendered silent by epigenetic pathways and heterochromatization. However, information on the behaviour of dominant NORs is very sparse and needed for an integrative knowledge of differential gene transcription levels and chromatin specific domain interactions.Methodology/Principal FindingsUsing molecular and cytological approaches in a wheat-rye addition line (wheat genome plus the rye nucleolar chromosome pair 1R), we investigated transcriptional activity and chromatin topology of the wheat dominant NORs in a nucleolar dominance situation. Herein we report dominant NORs up-regulation in the addition line through quantitative real-time PCR and silver-staining technique. Accompanying this modification in wheat rDNA trascription level, we also disclose that perinucleolar knobs of ribosomal chromatin are almost transcriptionally silent due to the residual detection of BrUTP incorporation in these domains, contrary to the marked labelling of intranucleolar condensed rDNA. Further, by comparative confocal analysis of nuclei probed to wheat and rye NORs, we found that in the wheat-rye addition line there is a significant decrease in the number of wheat-origin perinucleolar rDNA knobs, corresponding to a diminution of the rDNA heterochromatic fraction of the dominant (wheat) NORs.Conclusions/SignificanceWe demonstrate that inter-specific interactions leading to wheat-origin NOR dominance results not only on the silencing of rye origin NOR loci, but dominant NORs are also modified in their transcriptional activity and interphase organization. The results show a cross-talk between wheat and rye NORs, mediated by ribosomal chromatin dynamics, revealing a conceptual shift from differential amphiplasty to ‘mutual amphiplasty’ in the nucleolar dominance process.

Highlights

  • Chromatin, the living form of genetic information in eukaryotes, has particular organization and distribution patterns in the nucleus that are related to gene expression as observed in several biological systems, ranging from animals to plants

  • Conclusions/Significance: We demonstrate that inter-specific interactions leading to wheat-origin nucleolar organizing regions (NORs) dominance results on the silencing of rye origin NOR loci, but dominant NORs are modified in their transcriptional activity and interphase organization

  • We report that nucleolar dominance is a process where NORs of both parental species are modified in the wheat-rye combination, in contrary to the differential amphiplasty concept as described by Navashin in 1930s [19] affecting only underdominant NORs

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Summary

Introduction

The living form of genetic information in eukaryotes, has particular organization and distribution patterns in the nucleus that are related to gene expression as observed in several biological systems, ranging from animals to plants. Additional significance of heterochromatin relies on its involvement in the RNA interference pathways that lead to transcriptional and posttranscriptional gene silencing [5]. Chromosome domains and their topology, in addition to other functionally relevant nuclear landscapes (e.g, transcription foci, RNA processing, DNA repair), point to the importance of functional compartmentalization of the nucleus [6]. Chromatin organizational and topological plasticity, and its functions in gene expression regulation, have been strongly revealed by the analysis of nucleolar dominance in hybrids and polyploids where one parental set of ribosomal RNA (rDNA) genes that are clustered in nucleolar organizing regions (NORs), is rendered silent by epigenetic pathways and heterochromatization. Information on the behaviour of dominant NORs is very sparse and needed for an integrative knowledge of differential gene transcription levels and chromatin specific domain interactions

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