Abstract

Ribosomal RNA genes (rDNAs) are located in large domains of hundreds of rDNA units organized in a head-to-tail manner. The proper and stable inheritance of rDNA clusters is of paramount importance for survival. Yet, these highly repetitive elements pose a potential risk to the genome since they can undergo non-allelic exchanges. Here, we review the current knowledge of the organization of the rDNA clusters in Arabidopsis thaliana and their stability during meiosis. Recent findings suggest that during meiosis, all rDNA loci are embedded within the nucleolus favoring non-homologous end joining (NHEJ) as a repair mechanism, while DNA repair via homologous recombination (HR) appears to be a rare event. We propose a model where (1) frequent meiotic NHEJ events generate abundant single nucleotide polymorphisms and insertions/deletions within the rDNA, resulting in a heterogeneous population of rDNA units and (2) rare HR events dynamically change rDNA unit numbers, only to be observed in large populations over many generations. Based on the latest efforts to delineate the entire rDNA sequence in A. thaliana, we discuss evidence supporting this model. The results compiled so far draw a surprising picture of rDNA sequence heterogeneity between individual units. Furthermore, rDNA cluster sizes have been recognized as relatively stable when observing less than 10 generations, yet emerged as major determinant of genome size variation between different A. thaliana ecotypes. The sequencing efforts also revealed that transcripts from the diverse rDNA units yield heterogenous ribosome populations with potential functional implications. These findings strongly motivate further research to understand the mechanisms that maintain the metastable state of rDNA loci.

Highlights

  • The central importance of the rRNA genes for the biology of any organism is evident, as they are essential for survival and for all cellular processes

  • We provide a model, in agreement with the current data, that defines homologous recombination (HR) and non-homologous end joining (NHEJ) as the major determinants of rDNA cluster size and rDNA unit sequence variability

  • We suggest that doublestrand breaks (DSBs) within the rDNA, occurring at physiological levels, are repaired via NHEJ, preserving rDNA unit numbers and unit-internal repeat structures, but at the cost of producing errors

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Summary

Introduction

The central importance of the rRNA genes for the biology of any organism is evident, as they are essential for survival and for all cellular processes. C/a-NHEJ factors, such as LIG4 and MRE11, have been shown to be important for DNA repair within the rDNA region, whereas HDA6 and NUC2, which are involved in regulating rDNA transcription and nucleolus integrity, are essential for limiting HR at the rDNA (Sims et al, 2019).

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