Evidence map›Paper›PMID 27821753›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Selective nucleolus organizer inactivation in Arabidopsis is a chromosome position-effect phenomenon.

Gireesha Mohannath, Frederic Pontvianne, Craig S Pikaard

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
13.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. First draft genome of the decaploid species,GigaByte (Hong Kong, China) · 2026
    Article
  3. Regulation of nucleolar dominance through allopolyploidization of hexaploid wheat.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Reaching for the off switch in nucleolar dominance.The Plant journal : for cell and molecular biology · 2023
    Article
  9. Article
  10. Article
  11. Under the magnifying glass: The ups and downs of rDNA copy number.Seminars in cell & developmental biology · 2023
    Review
  12. Uniparental expression of ribosomal RNA in ×Frontiers in plant science · 2023
    Article
  13. Review
  14. Article
  15. The integrative biology of genetic dominance.Biological reviews of the Cambridge Philosophical Society · 2021
    Review
  16. Review
  17. Modeling the 3D genome of plants.Nucleus (Austin, Tex.) · 2021
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 2 countries.

Gireesha MohannathDepartment of Biology, Indiana University, Bloomington, IN 47405.
Frederic PontvianneLaboratoire Genome et Developpement des Plantes, UMR 5096, Université de Perpignan Via Domitia, 66860 Perpignan, France.
Craig S PikaardDepartment of Biology, Indiana University, Bloomington, IN 47405; cpikaard@indiana.edu.ORCID 0000-0001-8204-7459
Howard Hughes Medical Institute · USIndiana University Bloomington · USUniversité de Perpignan · FR

Funding

MOLECULAR GENETICS OF NUCLEOLAR DOMINANCER01GM060380 · NIGMS · WASHINGTON UNIVERSITY · PI PIKAARD, CRAIG STUART · 2000 to 2012
$3.3M
NIGMS NIH HHS R01 GM060380
6 · The paper itself

Abstract

Nucleolus organizer regions (NORs) are chromosomal loci where hundreds of rRNA genes are clustered. Despite being nearly identical in sequence, specific rRNA genes are selected for silencing during development via choice mechanism(s) that remain unclear. In Arabidopsis thaliana, rRNA gene subtypes that are silenced during development were recently mapped to the NOR on chromosome 2, NOR2, whereas active rRNA genes map to NOR4, on chromosome 4. In a mutant line deficient for ATXR5 or ATXR6-dependent histone H3 lysine 27 (H3K27) monomethylation, we show that millions of base pairs of chromosome 4, including the telomere, TEL4N, and much of NOR4, have been converted to the corresponding sequences of chromosome 2. This genomic change places rRNA genes of NOR2, which are normally silenced, at the position on chromosome 4 where active rRNA genes are normally located. At their new location, NOR2-derived rRNA genes escape silencing, independent of the atxr mutations, indicating that selective rRNA gene silencing is chromosome 2-specific. The chromosome 2 position effect is not explained by the NOR2-associated telomere, TEL2N, which remains linked to the translocated NOR, implicating centromere-proximal sequences in silencing.

Indexed as

ArabidopsisArabidopsis ProteinsBase SequenceChromosomal Position EffectsChromosomes, PlantCrosses, GeneticGene Expression Regulation, PlantGene SilencingGenes, PlantGenotypeHybridization, GeneticModels, GeneticNucleolus Organizer RegionRNA, RibosomalTelomereArabidopsis ProteinsRNA, Ribosomalchromosome translocationepigenetic regulationgene silencingnucleolar dominanceribosomal RNA

Identifiers

PMID27821753
PMCPMC5127337
OpenAlexW2551668844

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.