Evidence map›Paper›PMID 37776366›Full record

ArticleGigaScience2022

A chromosome-level assembly supports genome-wide investigation of the DMRT gene family in the golden mussel (Limnoperna fortunei).

João Gabriel R N Ferreira, Juliana A Americo, Danielle L A S do Amaral, Fábio Sendim, Yasmin R da Cunha, Tree of Life Programme, Mark Blaxter, Marcela Uliano-Silva, Mauro de F Rebelo

Abstract read
In one paragraph

Article in GigaScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Rapid turnover of sex-determining architecture in invasive mussels.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. High-quality chromosome-level genome assembly of the Northern Pacific sea star Asterias amurensis.DNA research : an international journal for rapid publication of reports on genes and genomes · 2024
    Article
  4. 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.

João Gabriel R N FerreiraBio Bureau Biotecnologia, Rio de Janeiro 21941-850, Brazil.ORCID 0000-0002-5226-7159
Juliana A AmericoBio Bureau Biotecnologia, Rio de Janeiro 21941-850, Brazil.ORCID 0000-0001-9443-6144
Danielle L A S do AmaralBio Bureau Biotecnologia, Rio de Janeiro 21941-850, Brazil.ORCID 0000-0002-8490-7464
Fábio SendimBio Bureau Biotecnologia, Rio de Janeiro 21941-850, Brazil.ORCID 0000-0002-8205-6416
Yasmin R da CunhaBio Bureau Biotecnologia, Rio de Janeiro 21941-850, Brazil.ORCID 0000-0003-4832-2167
Tree of Life Programme
Mark BlaxterTree of Life, Wellcome Sanger Institute, Hinxton CB10 1RQ, UK.ORCID 0000-0003-2861-949X
Marcela Uliano-SilvaTree of Life, Wellcome Sanger Institute, Hinxton CB10 1RQ, UK.ORCID 0000-0001-6723-4715
Mauro de F RebeloInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941-170, Brazil.ORCID 0000-0002-7809-0486

Funding

Wellcome TrustWellcome Trust 220540/Z/20/A
6 · The paper itself

Abstract

backgroundThe golden mussel (Limnoperna fortunei) is a highly invasive species that causes environmental and socioeconomic losses in invaded areas. Reference genomes have proven to be a valuable resource for studying the biology of invasive species. While the current golden mussel genome has been useful for identifying new genes, its high fragmentation hinders some applications.

findingsIn this study, we provide the first chromosome-level reference genome for the golden mussel. The genome was built using PacBio HiFi, 10X, and Hi-C sequencing data. The final assembly contains 99.4% of its total length assembled to the 15 chromosomes of the species and a scaffold N50 of 97.05 Mb. A total of 34,862 protein-coding genes were predicted, of which 84.7% were functionally annotated. A significant (6.48%) proportion of the genome was found to be in a hemizygous state. Using the new genome, we have performed a genome-wide characterization of the Doublesex and Mab-3 related transcription factor gene family, which has been proposed as a target for population control strategies in other species.

conclusionsFrom the applied research perspective, a higher-quality genome will support genome editing with the aim of developing biotechnology-based solutions to control invasion. From the basic research perspective, the new genome is a high-quality reference for molecular evolutionary studies of Mytilida and other Lophotrochozoa, and it may be used as a reference for future resequencing studies to assess genomic variation among different golden mussel populations, unveiling potential routes of dispersion and helping to establish better control policies.

Indexed as

MytilidaeAdenosine TriphosphateAnimalsChromosomesGenomeThionucleosidesAdenosine Triphosphate(S-dinitrophenyl)-6-mercaptopurine riboside triphosphateThionucleosidesDMRTgenomegolden musselinvasive speciesLimnoperna fortuneisex differentiation

Identifiers

PMID37776366
PMCPMC10541798

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LicenceCC BY
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Registered trials

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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.