Evidence map›Paper›PMID 24979765›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

SPR-5 and MET-2 function cooperatively to reestablish an epigenetic ground state during passage through the germ line.

Shana C Kerr, Chelsey Chandler Ruppersburg, Joshua W Francis, David J Katz

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Changing minds epigenetically: Germline genes in neurons disrupt animal behavior.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Ectopic transcription due to inherited histone methylation may interfere with the ongoing function of differentiated neurons.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Sterility in the offspring ofmicroPublication biology · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Development (Cambridge, England) · 2021
    Article
  18. Article
  19. Review
  20. Article
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

4 authors at 2 institutions in 1 country.

Shana C KerrSchool of Biology, Georgia Institute of Technology, Atlanta, GA 30332;Fellowships in Research and Science Teaching and.
Chelsey Chandler RuppersburgDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322;Graduate Division of Biological and Biomedical Science, Emory University, Atlanta, GA 30322; and.
Joshua W FrancisGraduate Division of Biological and Biomedical Science, Emory University, Atlanta, GA 30322; andDepartment of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322.
David J KatzDepartment of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322; djkatz@emory.edu.
Emory University · USGeorgia Institute of Technology · US

Funding

Training Program in Biochemistry, Cell and Molecular BiologyT32GM008367 · NIGMS · EMORY UNIVERSITY · PI BOISE, LAWRENCE H., CORBETT, ANITA H. · 1990 to 2019
$5.6M
NIGMS NIH HHS 5T32GM008367NIGMS NIH HHS T32 GM008367
6 · The paper itself

Abstract

The Caenorhabditis elegans LSD1 H3K4me2 demethylase SPR-5 reprograms epigenetic transcriptional memory during passage through the germ line. Here we show that mutants in the H3K9me2 methyltransferase, met-2, result in transgenerational epigenetic effects that parallel spr-5 mutants. In addition, we find that spr-5;met-2 double mutants have a synergistic effect on sterility, H3K4me2, and spermatogenesis expression. These results implicate MET-2 as a second histone-modifying enzyme in germ-line reprogramming and suggest a model in which SPR-5 and MET-2 function cooperatively to reestablish an epigenetic ground state required for the continued immortality of the C. elegans germ line. Without SPR-5 and MET-2, we find that the ability to express spermatogenesis genes is transgenerationally passed on to the somatic cells of the subsequent generation. This indicates that H3K4me2 may act in the maintenance of cell fate. Finally, we demonstrate that reducing H3K4me2 causes a large increase in H3K9me2 added by the SPR-5;MET-2 reprogramming mechanism. This finding suggests a novel histone code interaction in which the input chromatin environment dictates the output chromatin state. Taken together, our results provide evidence for a broader reprogramming mechanism in which multiple enzymes coordinately regulate histone information during passage through the germ line.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsChromatin ImmunoprecipitationDNA PrimersEpigenesis, GeneticGerm CellsHistone-Lysine N-MethyltransferaseHistonesInheritance PatternsMicroscopy, InterferenceModels, GeneticOxidoreductases, N-DemethylatingSpermatogenesisCaenorhabditis elegans ProteinsDNA PrimersHistone-Lysine N-MethyltransferaseHistonesMet-2 protein, C elegansOxidoreductases, N-DemethylatingSPR-5 protein, C elegans

Identifiers

PMID24979765
PMCPMC4084444
OpenAlexW2080406993

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.