Abstract
Background : The white shark ( Carcharodon carcharias ) is a globally distributed, apex predator possessing physical, physiological, and behavioral traits that have garnered it significant public attention. In addition to interest in the genetic basis of its form and function, as a representative of the oldest extant jawed vertebrate lineage, white sharks are also of conservation concern due to their small population size and threat from overfishing. Despite this, surprisingly little is known about the biology of white sharks, and genomic resources are unavailable. To address this deficit, we combined Roche-454 and Illumina sequencing technologies to characterize the first transcriptome of any tissue for this species.
Results : From white shark heart cDNA we generated 665,399 Roche 454 reads (median length 387-bp) that were assembled into 141,626 contigs (mean length 503-bp). We also generated 78,566,588 Illumina reads, which we aligned to the 454 contigs producing 105,014 454/Illumina consensus sequences. To these, we added 3,432 non-singleton 454 contigs. By comparing these sequences to the UniProtKB/Swiss-Prot database we were able to annotate 21,019 translated open reading frames (ORFs) of ≥ 20 amino acids. Of these, 19,277 were additionally assigned Gene Ontology (GO) functional annotations. While acknowledging the limitations of our single tissue transcriptome, Fisher tests showed the white shark transcriptome to be significantly enriched for numerous metabolic GO terms compared to the zebra fish and human transcriptomes, with white shark showing more similarity to human than to zebra fish (i.e. fewer terms were significantly different). We also compared the transcriptome to other available elasmobranch sequences, for signatures of positive selection and identified several genes of putative adaptive significance on the white shark lineage. The white shark transcriptome also contained 8,404 microsatellites (dinucleotide, trinucleotide, or tetranucleotide motifs ≥ five perfect repeats). Detailed characterization of these microsatellites showed that ORFs with trinucleotide repeats, were significantly enriched for transcription regulatory roles and that trinucleotide frequency within ORFs was lower than for a wide range of taxonomic groups including other vertebrates.
Conclusion : The white shark heart transcriptome represents a valuable resource for future elasmobranch functional and comparative genomic studies, as well as for population and other biological studies vital for effective conservation of this globally vulnerable species.
| Original language | American English |
|---|---|
| Article number | 697 |
| Journal | BMC Genomics |
| Volume | 14 |
| DOIs | |
| State | Published - Oct 11 2013 |
Funding
We are very grateful to Dr. L. Natanson (NOAA NEFSC) for providing the white shark heart and the NOAA Office for Law Enforcement for making the confiscated shark carcass available for scientific study. We thank the Cornell Life Sciences Core Laboratory for performing the 454 and Illumina sequencing, and we are grateful to Qi Sun and Jaroslaw Pillardy for their assistance with the bioinformatics analyses. This study was supported by grants from the Save Our Seas Foundation, Guy Harvey Ocean Foundation, and Hai Stiftung/Shark Foundation to MSS.
| Funders |
|---|
| Hai Stiftung/Shark Foundation |
| Guy Harvey Ocean Foundation |
| Save our Seas Foundation |
ASJC Scopus Subject Areas
- Genetics
- Biotechnology
Keywords
- Carcharodon carcharias
- Enrichment
- Heart transcriptome
- Microsatellites
- Positive selection
- White shark
- Molecular Sequence Annotation
- Open Reading Frames
- Selection, Genetic
- Transcriptome
- Untranslated Regions
- Sequence Analysis, DNA
- Animals
- Myocardium/metabolism
- Sharks/genetics
- High-Throughput Nucleotide Sequencing
- Fish Proteins/genetics
- Gene Ontology
- Microsatellite Repeats
- Evolution, Molecular
Disciplines
- Genetics and Genomics
- Marine Biology
- Oceanography and Atmospheric Sciences and Meteorology
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