Evidence map›Paper›PMID 31960924›Full record

ArticleMolecular biology and evolution2020

Evolution of Transcriptional Repressors Impacts Caenorhabditis Vulval Development.

Helen M Chamberlin, Ish M Jain, Marcos Corchado-Sonera, Leanne H Kelley, Devika Sharanya, Abdulrahman Jama, Romy Pabla, Adriana T Dawes, Bhagwati P Gupta

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  4. Characterization of two newmicroPublication biology · 2023
    Article
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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 at 2 institutions in 2 countries.

Helen M ChamberlinDepartment of Molecular Genetics, Ohio State University, Columbus, OH.
Ish M JainDepartment of Biology, McMaster University, Hamilton, ON, Canada.
Marcos Corchado-SoneraDepartment of Molecular Genetics, Ohio State University, Columbus, OH.
Leanne H KelleyDepartment of Molecular Genetics, Ohio State University, Columbus, OH.
Devika SharanyaDepartment of Biology, McMaster University, Hamilton, ON, Canada.
Abdulrahman JamaDepartment of Molecular Genetics, Ohio State University, Columbus, OH.
Romy PablaDepartment of Biology, McMaster University, Hamilton, ON, Canada.
Adriana T DawesDepartment of Molecular Genetics, Ohio State University, Columbus, OH.
Bhagwati P GuptaDepartment of Biology, McMaster University, Hamilton, ON, Canada.
The Ohio State University · USMcMaster University · CA

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Cellular, molecular, and biochemical sciences training grantT32GM086252 · NIGMS · OHIO STATE UNIVERSITY · PI JACKMAN, JANE ELIZABETH, MUSIER-FORSYTH, KARIN M · 2011 to 2020
$2.0M
NCI NIH HHS P30 CA016058NIGMS NIH HHS T32 GM086252NIH HHS P40 OD010440
6 · The paper itself

Abstract

Comparative genomic sequence analysis has found that the genes for many chromatin-associated proteins are poorly conserved, but the biological consequences of these sequence changes are not understood. Here, we show that four genes identified for an Inappropriate Vulval cell Proliferation (ivp) phenotype in the nematode Caenorhabditis briggsae exhibit distinct functions and genetic interactions when compared with their orthologs in C. elegans. Specifically, we show that the four C. briggsae ivp genes encode the noncanonical histone HTZ-1/H2A.z and three nematode-specific proteins predicted to function in the nucleus. The mutants exhibit ectopic vulval precursor cell proliferation (the multivulva [Muv] phenotype) due to inappropriate expression of the lin-3/EGF gene, and RNAseq analysis suggests a broad role for these ivp genes in transcriptional repression. Importantly, although the C. briggsae phenotypes have parallels with those seen in the C. elegans synMuv system, except for the highly conserved HTZ-1/H2A.z, comparable mutations in C. elegans ivp orthologs do not exhibit synMuv gene interactions or phenotypes. These results demonstrate the evolutionary changes that can underlie conserved biological outputs and argue that proteins critical to repress inappropriate expression from the genome participate in a rapidly evolving functional landscape.

Indexed as

Evolution, MolecularGene Expression Regulation, DevelopmentalAnimalsCaenorhabditisFemaleHistonesNuclear ProteinsVulvaHistonesNuclear Proteinschromatindevelopmental evolutiondevelopmental system drifttranscriptional repression

Identifiers

PMID31960924
PMCPMC7182219
OpenAlexW3002184483

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.