Evidence map›Paper›PMID 39567907›Full record

ArticleBMC genomics2024

Chromosome-level genome assemblies and genetic maps reveal heterochiasmy and macrosynteny in endangered Atlantic Acropora.

Nicolas S Locatelli, Sheila A Kitchen, Kathryn H Stankiewicz, C Cornelia Osborne, Zoe Dellaert, Holland Elder, Bishoy Kamel, Hanna R Koch, Nicole D Fogarty, Iliana B Baums

Abstract read
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Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Genome assembly and annotation ofGigaByte (Hong Kong, China) · 2025
    Article
  7. Article
  8. Genomes of the Caribbean reef-building coralsbioRxiv : the preprint server for biology · 2024
    Article
4 · The record

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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

10 authors.

Nicolas S Locatelli *Department of Biology, The Pennsylvania State University, University Park, PA, USA.ORCID http://orcid.org/0000-0001-7850-5015
Sheila A Kitchen *Department of Biology, The Pennsylvania State University, University Park, PA, USA.ORCID http://orcid.org/0000-0003-4402-8139
Kathryn H Stankiewicz *Department of Biology, The Pennsylvania State University, University Park, PA, USA.ORCID http://orcid.org/0000-0002-1904-5845
C Cornelia OsborneDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.ORCID http://orcid.org/0000-0001-6759-4542
Zoe DellaertDepartment of Biology, The Pennsylvania State University, University Park, PA, USA.ORCID http://orcid.org/0000-0003-4102-1492
Holland ElderAustralian Institute of Marine Science, Townsville, QLD, Australia.ORCID http://orcid.org/0000-0001-8432-4632
Bishoy KamelLawrence Berkeley National Laboratory, Joint Genome Institute, Berkeley, CA, USA.ORCID http://orcid.org/0000-0003-2934-3827
Hanna R KochMote Marine Laboratory, Coral Reef Restoration Program, Summerland Key, FL, USA.ORCID http://orcid.org/0000-0002-1776-9487
Nicole D FogartyDepartment of Biology and Marine Biology, University of North Carolina Wilmington, Wilmington, NC, USA.ORCID http://orcid.org/0000-0003-3811-3791
Iliana B BaumsDepartment of Biology, The Pennsylvania State University, University Park, PA, USA. iliana.baums@hifmb.de.ORCID http://orcid.org/0000-0001-6463-7308

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver their evolutionary history, corals have adapted to sea level rise and increasing ocean temperatures, however, it is unclear how quickly they may respond to rapid change. Genome structure and genetic diversity contained within may highlight their adaptive potential.

resultsWe present chromosome-scale genome assemblies and linkage maps of the critically endangered Atlantic acroporids, Acropora palmata and A. cervicornis. Both assemblies and linkage maps were resolved into 14 chromosomes with their gene content and colinearity. Repeats and chromosome arrangements were largely preserved between the species. The family Acroporidae and the genus Acropora exhibited many phylogenetically significant gene family expansions. Macrosynteny decreased with phylogenetic distance. Nevertheless, scleractinians shared six of the 21 cnidarian ancestral linkage groups as well as numerous fission and fusion events compared to other distantly related cnidarians. Genetic linkage maps were constructed from one A. palmata family and 16 A. cervicornis families using a genotyping array. The consensus maps span 1,013.42 cM and 927.36 cM for A. palmata and A. cervicornis, respectively. Both species exhibited high genome-wide recombination rates (3.04 to 3.53 cM/Mb) and pronounced sex-based differences, known as heterochiasmy, with 2 to 2.5X higher recombination rates estimated in the female maps.

conclusionsTogether, the chromosome-scale assemblies and genetic maps we present here are the first detailed look at the genomic landscapes of the critically endangered Atlantic acroporids. These data sets revealed that adaptive capacity of Atlantic acroporids is not limited by their recombination rates. The sister species maintain macrosynteny with few genes with high sequence divergence that may act as reproductive barriers between them. In the Atlantic Acropora, hybridization between the two sister species yields an F1 hybrid with limited fertility despite the high levels of macrosynteny and gene colinearity of their genomes. Together, these resources now enable genome-wide association studies and discovery of quantitative trait loci, two tools that can aid in the conservation of these species.

Indexed as

AnthozoaChromosome MappingEndangered SpeciesAnimalsChromosomesGenetic LinkageGenomeGenomicsPhylogenySyntenyAcroporaAncestral linkage groupChromosomeCoralGenomeHermaphroditeHeterochiasmyLinkage mapRecombination rate

Identifiers

PMID39567907
PMCPMC11577847

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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.