Evidence map›Paper›PMID 28893194›Full record

ArticleBMC genomics2017

De novo metatranscriptome assembly and coral gene expression profile of Montipora capitata with growth anomaly.

Monika Frazier, Martin Helmkampf, M Renee Bellinger, Scott M Geib, Misaki Takabayashi

Abstract read
In one paragraph

Article in BMC genomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Interspecies Communication in Holobionts by Non-Coding RNA Exchange.International journal of molecular sciences · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. 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

5 authors.

Monika FrazierTropical Conservation Biology and Environmental Science, University of Hawai'i at Hilo, 200 West Kāwili Street, Hilo, HI, 96720, USA.
Martin HelmkampfTropical Conservation Biology and Environmental Science, University of Hawai'i at Hilo, 200 West Kāwili Street, Hilo, HI, 96720, USA.
M Renee BellingerTropical Conservation Biology and Environmental Science, University of Hawai'i at Hilo, 200 West Kāwili Street, Hilo, HI, 96720, USA.
Scott M GeibUnited States Department of Agriculture, Agriculture Research Service, Daniel K Inouye U.S. Pacific Basin Agricultural Research Center, 64 Nowelo St, Hilo, HI, 96720, USA.
Misaki TakabayashiTropical Conservation Biology and Environmental Science, University of Hawai'i at Hilo, 200 West Kāwili Street, Hilo, HI, 96720, USA. misakita@hawaii.edu.ORCID http://orcid.org/0000-0003-3921-3188

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundScleractinian corals are a vital component of coral reef ecosystems, and of significant cultural and economic value worldwide. As anthropogenic and natural stressors are contributing to a global decline of coral reefs, understanding coral health is critical to help preserve these ecosystems. Growth anomaly (GA) is a coral disease that has significant negative impacts on coral biology, yet our understanding of its etiology and pathology is lacking. In this study we used RNA-seq along with de novo metatranscriptome assembly and homology assignment to identify coral genes that are expressed in three distinct coral tissue types: tissue from healthy corals ("healthy"), GA lesion tissue from diseased corals ("GA-affected") and apparently healthy tissue from diseased corals ("GA-unaffected"). We conducted pairwise comparisons of gene expression among these three tissue types to identify genes and pathways that help us to unravel the molecular pathology of this coral disease.

resultsThe quality-filtered de novo-assembled metatranscriptome contained 76,063 genes, of which 13,643 were identified as putative coral genes. Overall gene expression profiles of coral genes revealed high similarity between healthy tissue samples, in contrast to high variance among diseased samples. This indicates GA has a variety of genetic effects at the colony level, including on seemingly healthy (GA-unaffected) tissue. A total of 105 unique coral genes were found differentially expressed among tissue types. Pairwise comparisons revealed the greatest number of differentially expressed genes between healthy and GA-affected tissue (93 genes), followed by healthy and GA-unaffected tissue (33 genes), and GA-affected and -unaffected tissue (7 genes). The putative function of these genes suggests GA is associated with changes in the activity of genes involved in developmental processes and activation of the immune system.

conclusionThis is one of the first transcriptome-level studies to investigate coral GA, and the first metatranscriptome assembly for the M. capitata holobiont. The gene expression data, metatranscriptome assembly and methodology developed through this study represent a significant addition to the molecular information available to further our understanding of this coral disease.

Indexed as

Gene Expression ProfilingAnimalsAnthozoaMorphogenesisCoral diseaseGene expressionGrowth anomalyMetatranscriptomeMontipora capitataRNA-seq

Identifiers

PMID28893194
PMCPMC5594617

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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.