Evidence map›Paper›PMID 30419815›Full record

ArticleBMC evolutionary biology2018

Double maternal-effect: duplicated nucleoplasmin 2 genes, npm2a and npm2b, with essential but distinct functions are shared by fish and tetrapods.

Caroline T Cheung, Jérémy Pasquier, Aurélien Bouleau, Thaovi Nguyen, Franck Chesnel, Yann Guiguen, Julien Bobe

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2018. 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
0.6field-weighted citation impact, top 39% 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, 13 citations in OpenAlex.

  1. Article
  2. Cells · 2022
    Article
  3. Histone Chaperones as Cardinal Players in Development.Frontiers in cell and developmental biology · 2022
    Review
  4. Article
  5. Influence of Parental Fatty Acid Desaturase 2 (Animals : an open access journal from MDPI · 2020
    Article
  6. Article
  7. PeerJ · 2018
    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

7 authors at 2 institutions in 1 country.

Caroline T CheungINRA LPGP UR1037, Campus de Beaulieu, 35042, Rennes, France.
Jérémy PasquierINRA LPGP UR1037, Campus de Beaulieu, 35042, Rennes, France.
Aurélien BouleauINRA LPGP UR1037, Campus de Beaulieu, 35042, Rennes, France.
Thaovi NguyenINRA LPGP UR1037, Campus de Beaulieu, 35042, Rennes, France.
Franck ChesnelCNRS/UMR6290, Université de Rennes 1, 35000, Rennes, France.
Yann GuiguenINRA LPGP UR1037, Campus de Beaulieu, 35042, Rennes, France.
Julien BobeINRA LPGP UR1037, Campus de Beaulieu, 35042, Rennes, France. julien.bobe@inra.fr.ORCID 0000-0002-9355-8227
Laboratoire de Physiologie et Génomique des Poissons · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNucleoplasmin 2 (npm2) is an essential maternal-effect gene that mediates early embryonic events through its function as a histone chaperone that remodels chromatin. Recently, two npm2 (npm2a and npm2b) genes have been annotated in zebrafish. Thus, we examined the evolution of npm2a and npm2b in a variety of vertebrates, their potential phylogenetic relationships, and their biological functions using knockout models via the CRISPR/cas9 system.

resultsWe demonstrated that the two npm2 duplicates exist in a wide range of vertebrates, including sharks, ray-finned fish, amphibians, and sauropsids, while npm2a was lost in coelacanth and mammals, as well as some specific teleost lineages. Using phylogeny and synteny analyses, we traced their origins to the early stages of vertebrate evolution. Our findings suggested that npm2a and npm2b resulted from an ancient local gene duplication, and their functions diverged although key protein domains were conserved. We then investigated their functions by examining their tissue distribution in a wide variety of species and found that they shared ovarian-specific expression, a key feature of maternal-effect genes. We also demonstrated that both npm2a and npm2b are maternally-inherited transcripts in vertebrates, and that they play essential, but distinct, roles in early embryogenesis using zebrafish knockout models. Both npm2a and npm2b function early during oogenesis and may play a role in cortical granule function that impact egg activation and fertilization, while npm2b is also involved in early embryogenesis.

conclusionThese novel findings will broaden our knowledge on the evolutionary history of maternal-effect genes and underlying mechanisms that contribute to vertebrate reproductive success. In addition, our results demonstrate the existence of a newly described maternal-effect gene, npm2a, that contributes to egg competence, an area that still requires further comprehension.

Indexed as

Genes, DuplicateAnimalsConserved SequenceEvolution, MolecularFemaleFishesGene DuplicationGene Expression ProfilingGenomeHumansNucleoplasminsPeptidesPhylogenyProtein DomainsSyntenyZebrafishNucleoplasminsPeptidesZebrafish ProteinsCRISPR-cas9 knockoutEvolutionMaternal-effect genesnpm2Vertebrates

Identifiers

PMID30419815
PMCPMC6233590
OpenAlexW2901125180

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.