Evidence map›Paper›PMID 23937070›Full record

ArticleBMC genomics2013

Transcriptome deep-sequencing and clustering of expressed isoforms from Favia corals.

Shaadi F Pooyaei Mehr, Rob DeSalle, Hung-Teh Kao, Apurva Narechania, Zhou Han, Dan Tchernov, Vincent Pieribone, David F Gruber

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Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

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12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Reefgenomics.Org - a repository for marine genomics data.Database : the journal of biological databases and curation · 2016
    Article
  7. Article
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  10. Review
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  12. Review
4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Shaadi F Pooyaei MehrThe Graduate Center, Molecular, Cellular and Developmental Biology, City University of New York, New York, NY 10065, USA. fpooyaei-mehr@amnh.org
Rob DeSalle
Hung-Teh Kao
Apurva Narechania
Zhou Han
Dan Tchernov
Vincent Pieribone
David F Gruber

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGenomic and transcriptomic sequence data are essential tools for tackling ecological problems. Using an approach that combines next-generation sequencing, de novo transcriptome assembly, gene annotation and synthetic gene construction, we identify and cluster the protein families from Favia corals from the northern Red Sea.

resultsWe obtained 80 million 75 bp paired-end cDNA reads from two Favia adult samples collected at 65 m (Fav1, Fav2) on the Illumina GA platform, and generated two de novo assemblies using ABySS and CAP3. After removing redundancy and filtering out low quality reads, our transcriptome datasets contained 58,268 (Fav1) and 62,469 (Fav2) contigs longer than 100 bp, with N50 values of 1,665 bp and 1,439 bp, respectively. Using the proteome of the sea anemone Nematostella vectensis as a reference, we were able to annotate almost 20% of each dataset using reciprocal homology searches. Homologous clustering of these annotated transcripts allowed us to divide them into 7,186 (Fav1) and 6,862 (Fav2) homologous transcript clusters (E-value ≤ 2e(-30)). Functional annotation categories were assigned to homologous clusters using the functional annotation of Nematostella vectensis. General annotation of the assembled transcripts was improved 1-3% using the Acropora digitifera proteome. In addition, we screened these transcript isoform clusters for fluorescent proteins (FPs) homologs and identified seven potential FP homologs in Fav1, and four in Fav2. These transcripts were validated as bona fide FP transcripts via robust fluorescence heterologous expression. Annotation of the assembled contigs revealed that 1.34% and 1.61% (in Fav1 and Fav2, respectively) of the total assembled contigs likely originated from the corals' algal symbiont, Symbiodinium spp.

conclusionsHere we present a study to identify the homologous transcript isoform clusters from the transcriptome of Favia corals using a far-related reference proteome. Furthermore, the symbiont-derived transcripts were isolated from the datasets and their contribution quantified. This is the first annotated transcriptome of the genus Favia, a major increase in genomics resources available in this important family of corals.

Indexed as

Gene Expression ProfilingHigh-Throughput Nucleotide SequencingAmino Acid SequenceAnimalsAnthozoaCluster AnalysisDinoflagellidaEvolution, MolecularGenomicsMolecular Sequence AnnotationMolecular Sequence DataPhylogenyRNA IsoformsRNA, MessengerSequence Homology, Amino AcidRNA IsoformsRNA, Messenger

Identifiers

PMID23937070
PMCPMC3751062

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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.