Evidence map›Paper›PMID 25343511›Full record

ArticleThe ISME journal2015

Unfolding the secrets of coral-algal symbiosis.

Nedeljka Rosic, Edmund Yew Siang Ling, Chon-Kit Kenneth Chan, Hong Ching Lee, Paulina Kaniewska, David Edwards, Sophie Dove, Ove Hoegh-Guldberg

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 114 citations in OpenAlex.

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  9. Osmotic stress response of the coral and oyster pathogenApplied and environmental microbiology · 2024
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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

8 authors at 4 institutions in 1 country.

Nedeljka RosicSchool of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia.
Edmund Yew Siang LingUniversity of Queensland Centre for Clinical Research, The University of Queensland, Herston, Queensland, Australia.
Chon-Kit Kenneth ChanSchool of Agriculture and Food Sciences, The University of Queensland, St Lucia, Queensland, Australia.
Hong Ching LeeThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, New South Wales, Australia.
Paulina Kaniewska1] School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia [2] Australian Institute of Marine Science, Townsville, Queensland, Australia.
David Edwards1] School of Agriculture and Food Sciences, The University of Queensland, St Lucia, Queensland, Australia [2] School of Plant Biology, University of Western Australia, Perth, Western Australia, Australia [3] Australian Centre for Plant Functional Genomics, The University of Queensland, St Lucia, Queensland, Australia.
Sophie Dove1] School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia [2] ARC Centre of Excellence for Coral Reef Studies, The University of Queensland, St Lucia, Queensland, Australia.
Ove Hoegh-Guldberg1] School of Biological Sciences, The University of Queensland, St Lucia, Queensland, Australia [2] ARC Centre of Excellence for Coral Reef Studies, The University of Queensland, St Lucia, Queensland, Australia [3] Global Change Institute and ARC Centre of Excellence for Coral Reef Studies, The University of Queensland, St Lucia, Queensland, Australia.
University of Queensland · AUARC Centre of Excellence for Coral Reef Studies · AUThe Kinghorn Cancer Centre · AUUniversity of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dinoflagellates from the genus Symbiodinium form a mutualistic symbiotic relationship with reef-building corals. Here we applied massively parallel Illumina sequencing to assess genetic similarity and diversity among four phylogenetically diverse dinoflagellate clades (A, B, C and D) that are commonly associated with corals. We obtained more than 30,000 predicted genes for each Symbiodinium clade, with a majority of the aligned transcripts corresponding to sequence data sets of symbiotic dinoflagellates and <2% of sequences having bacterial or other foreign origin. We report 1053 genes, orthologous among four Symbiodinium clades, that share a high level of sequence identity to known proteins from the SwissProt (SP) database. Approximately 80% of the transcripts aligning to the 1053 SP genes were unique to Symbiodinium species and did not align to other dinoflagellates and unrelated eukaryotic transcriptomes/genomes. Six pathways were common to all four Symbiodinium clades including the phosphatidylinositol signaling system and inositol phosphate metabolism pathways. The list of Symbiodinium transcripts common to all four clades included conserved genes such as heat shock proteins (Hsp70 and Hsp90), calmodulin, actin and tubulin, several ribosomal, photosynthetic and cytochrome genes and chloroplast-based heme-containing cytochrome P450, involved in the biosynthesis of xanthophylls. Antioxidant genes, which are important in stress responses, were also preserved, as were a number of calcium-dependent and calcium/calmodulin-dependent protein kinases that may play a role in the establishment of symbiosis. Our findings disclose new knowledge about the genetic uniqueness of symbiotic dinoflagellates and provide a list of homologous genes important for the foundation of coral-algal symbiosis.

Indexed as

SymbiosisAnimalsAnthozoaCoral ReefsDinoflagellidaGenome, ProtozoanPhylogenyProtozoan ProteinsTranscriptomeProtozoan Proteins

Identifiers

PMID25343511
PMCPMC4817714
OpenAlexW2060195827

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.