Evidence map›Paper›PMID 40460278›Full record

ArticleGenetics2025

A unified framework governing the establishment and maintenance of transgenerational epigenetic inheritance.

Rachel M Woodhouse, Natalya Frolows, Dhruv S Monteiro, Jessica J Hawes, Azelle Hawdon, Michael Davies, Owen Watson, Victoria S Lennox, Alyson Ashe

Abstract read
In one paragraph

Article in Genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

9 authors.

Rachel M WoodhouseCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Natalya FrolowsCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Dhruv S MonteiroCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Jessica J HawesCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Azelle HawdonCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Michael DaviesCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Owen WatsonCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Victoria S LennoxCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.
Alyson AsheCharles Perkins Centre, School of Life and Environmental Science, The University of Sydney, Sydney, NSW 2050, Australia.

Funding

Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Ann E. Rougvie · 2012 to 2026
$7.5M
Australian Government Research Training ProgramAustralian Research CouncilCSIRO Postgraduate Research Supplementary Scholarship DP200102904CSIRO Postgraduate Research Supplementary Scholarship DP240100725CSIRO Postgraduate Research Supplementary Scholarship FT180100653NIH HHS P40 OD010440
6 · The paper itself

Abstract

Transgenerational epigenetic inheritance (TEI) is the transfer of nongenetic information between generations. In Caenorhabditis elegans, RNA interference (RNAi) is a conserved process initiated by double-stranded RNA, which can induce TEI. While many factors have been implicated in TEI, whether they act in establishment or maintenance of the transgenerational signal, and the generation in which they act, has not been defined. Here, we characterize the actions of glh-1, hrde-1, -2, -4, morc-1, nrde-1, -2, -4, set-25, -32, wago-1, -4, znfx-1, pup-1, and emb-4 within RNAi-induced TEI. We show that these genes can be classified into 3 groups: those involved in only establishment or maintenance, or those involved in both. We identify a heterochromatin-based pathway established in the P0 generation by histone methyltransferases and maintained in later generations by MORC-1, upstream of HRDE-1-dependent silencing. By investigating lineage dynamics, we provide evidence that inheritance patterns are partially determined in RNAi-exposed parents, but that variation between offspring also contributes. And finally, we demonstrate that polyUG RNAs broadly correlate with, but do not define, inheritance patterns. Together, this work forms a cohesive model of RNAi-induced TEI.

Indexed as

Caenorhabditis elegansEpigenesis, GeneticInheritance PatternsAnimalsCaenorhabditis elegans ProteinsHeterochromatinHistone-Lysine N-MethyltransferaseRNA InterferenceCaenorhabditis elegans ProteinsHeterochromatinHistone-Lysine N-MethyltransferaseC. eleganschromatinepigenetic inheritanceepigeneticssmall RNAWormBase

Identifiers

PMID40460278
PMCPMC12341889

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.