Evidence map›Paper›PMID 29750268›Full record

ArticleNucleic acids research2018

Inferring and modeling inheritance of differentially methylated changes across multiple generations.

Pascal Belleau, Astrid Deschênes, Marie-Pier Scott-Boyer, Romain Lambrot, Mathieu Dalvai, Sarah Kimmins, Janice Bailey, Arnaud Droit

Erratum issuedAbstract read
In one paragraph

Article in Nucleic acids research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Pascal BelleauDépartement de Médecine Moléculaire - Université Laval, Faculté de médecine, Pavillon Ferdinand-Vandry, 1050 avenue de la Médecine, bureau 4633, Québec, QC G1V 0A6, Canada.
Astrid DeschênesCentre de Recherche du CHU de Québec - Université Laval, 2705 boulevard Laurier, Québec, QC G1V 4G2, Canada.
Marie-Pier Scott-BoyerCentre de Recherche du CHU de Québec - Université Laval, 2705 boulevard Laurier, Québec, QC G1V 4G2, Canada.
Romain LambrotDepartment of Animal Sciences, McGill University, Ste. Anne de Bellevue, Quebec, H9 × 3V9 Canada and Department of Pharmacology and Therapeutics, McGill University, Montréal, Québec H3G 1Y6, Canada.
Mathieu DalvaiCentre de recherche en reproduction, développement et santé intergénérationnelle - Université Laval, Faculté des sciences de l'agriculture et de l'alimentation, Pavillon Paul-Comtois, 2425 rue de l'Agriculture, Québec, QC G1V 0A6, Canada.
Sarah KimminsDepartment of Animal Sciences, McGill University, Ste. Anne de Bellevue, Quebec, H9 × 3V9 Canada and Department of Pharmacology and Therapeutics, McGill University, Montréal, Québec H3G 1Y6, Canada.
Janice BaileyCentre de recherche en reproduction, développement et santé intergénérationnelle - Université Laval, Faculté des sciences de l'agriculture et de l'alimentation, Pavillon Paul-Comtois, 2425 rue de l'Agriculture, Québec, QC G1V 0A6, Canada.
Arnaud DroitDépartement de Médecine Moléculaire - Université Laval, Faculté de médecine, Pavillon Ferdinand-Vandry, 1050 avenue de la Médecine, bureau 4633, Québec, QC G1V 0A6, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput methylation sequencing enables genome-wide detection of differentially methylated sites (DMS) or regions (DMR). Increasing evidence suggests that treatment-induced DMS can be transmitted across generations, but the analysis of induced methylation changes across multiple generations is complicated by the lack of sound statistical methods to evaluate significance levels. Due to software design, DMS detection was usually made on each generation separately, thus disregarding stochastic effects expected when a large number of DMS is detected in each generation. Here, we present a novel method based on Monte Carlo sampling, methylInheritance, to evaluate that the number of conserved DMS between several generations is associated to an effect inherited from a treatment and not randomness. Moreover, we developed an inheritance simulation package, methInheritSim, to demonstrate the performance of the methylInheritance method and to evaluate the power of different experimental designs. Finally, we applied methylInheritance to a DNA methylation dataset obtained from early-life persistent organic pollutants (POPs) exposed Sprague-Dawley female rats and their descendants through a paternal transmission. The results show that metylInheritance can efficiently identify treatment-induced inherited methylation changes. Specifically, we identified two intergenerationally conserved DMS at transcription start site (TSS); one of those persisted transgenerationally. Three transgenerationally conserved DMR were found at intra or integenic regions.

Indexed as

DNA MethylationInheritance PatternsAnimalsComputer SimulationEnvironmental PollutantsEpigenesis, GeneticFemaleMaleModels, GeneticMonte Carlo MethodRats, Sprague-DawleyEnvironmental Pollutants

Identifiers

PMID29750268
PMCPMC6101575

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.