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Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx
BACKGROUND: New methods are needed for genomic-scale analysis of emerging model organisms that exemplify important biological questions but lack fully sequenced genomes. For example, there is an urgent need to understand the potential for corals to adapt to climate change, but few molecular resource...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689275/ https://www.ncbi.nlm.nih.gov/pubmed/19435504 http://dx.doi.org/10.1186/1471-2164-10-219 |
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author | Meyer, Eli Aglyamova, Galina V Wang, Shi Buchanan-Carter, Jade Abrego, David Colbourne, John K Willis, Bette L Matz, Mikhail V |
author_facet | Meyer, Eli Aglyamova, Galina V Wang, Shi Buchanan-Carter, Jade Abrego, David Colbourne, John K Willis, Bette L Matz, Mikhail V |
author_sort | Meyer, Eli |
collection | PubMed |
description | BACKGROUND: New methods are needed for genomic-scale analysis of emerging model organisms that exemplify important biological questions but lack fully sequenced genomes. For example, there is an urgent need to understand the potential for corals to adapt to climate change, but few molecular resources are available for studying these processes in reef-building corals. To facilitate genomics studies in corals and other non-model systems, we describe methods for transcriptome sequencing using 454, as well as strategies for assembling a useful catalog of genes from the output. We have applied these methods to sequence the transcriptome of planulae larvae from the coral Acropora millepora. RESULTS: More than 600,000 reads produced in a single 454 sequencing run were assembled into ~40,000 contigs with five-fold average sequencing coverage. Based on sequence similarity with known proteins, these analyses identified ~11,000 different genes expressed in a range of conditions including thermal stress and settlement induction. Assembled sequences were annotated with gene names, conserved domains, and Gene Ontology terms. Targeted searches using these annotations identified the majority of genes associated with essential metabolic pathways and conserved signaling pathways, as well as novel candidate genes for stress-related processes. Comparisons with the genome of the anemone Nematostella vectensis revealed ~8,500 pairs of orthologs and ~100 candidate coral-specific genes. More than 30,000 SNPs were detected in the coral sequences, and a subset of these validated by re-sequencing. CONCLUSION: The methods described here for deep sequencing of the transcriptome should be widely applicable to generate catalogs of genes and genetic markers in emerging model organisms. Our data provide the most comprehensive sequence resource currently available for reef-building corals, and include an extensive collection of potential genetic markers for association and population connectivity studies. The characterization of the larval transcriptome for this widely-studied coral will enable research into the biological processes underlying stress responses in corals and evolutionary adaptation to global climate change. |
format | Text |
id | pubmed-2689275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26892752009-06-02 Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx Meyer, Eli Aglyamova, Galina V Wang, Shi Buchanan-Carter, Jade Abrego, David Colbourne, John K Willis, Bette L Matz, Mikhail V BMC Genomics Research Article BACKGROUND: New methods are needed for genomic-scale analysis of emerging model organisms that exemplify important biological questions but lack fully sequenced genomes. For example, there is an urgent need to understand the potential for corals to adapt to climate change, but few molecular resources are available for studying these processes in reef-building corals. To facilitate genomics studies in corals and other non-model systems, we describe methods for transcriptome sequencing using 454, as well as strategies for assembling a useful catalog of genes from the output. We have applied these methods to sequence the transcriptome of planulae larvae from the coral Acropora millepora. RESULTS: More than 600,000 reads produced in a single 454 sequencing run were assembled into ~40,000 contigs with five-fold average sequencing coverage. Based on sequence similarity with known proteins, these analyses identified ~11,000 different genes expressed in a range of conditions including thermal stress and settlement induction. Assembled sequences were annotated with gene names, conserved domains, and Gene Ontology terms. Targeted searches using these annotations identified the majority of genes associated with essential metabolic pathways and conserved signaling pathways, as well as novel candidate genes for stress-related processes. Comparisons with the genome of the anemone Nematostella vectensis revealed ~8,500 pairs of orthologs and ~100 candidate coral-specific genes. More than 30,000 SNPs were detected in the coral sequences, and a subset of these validated by re-sequencing. CONCLUSION: The methods described here for deep sequencing of the transcriptome should be widely applicable to generate catalogs of genes and genetic markers in emerging model organisms. Our data provide the most comprehensive sequence resource currently available for reef-building corals, and include an extensive collection of potential genetic markers for association and population connectivity studies. The characterization of the larval transcriptome for this widely-studied coral will enable research into the biological processes underlying stress responses in corals and evolutionary adaptation to global climate change. BioMed Central 2009-05-12 /pmc/articles/PMC2689275/ /pubmed/19435504 http://dx.doi.org/10.1186/1471-2164-10-219 Text en Copyright © 2009 Meyer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Meyer, Eli Aglyamova, Galina V Wang, Shi Buchanan-Carter, Jade Abrego, David Colbourne, John K Willis, Bette L Matz, Mikhail V Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx |
title | Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx |
title_full | Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx |
title_fullStr | Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx |
title_full_unstemmed | Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx |
title_short | Sequencing and de novo analysis of a coral larval transcriptome using 454 GSFlx |
title_sort | sequencing and de novo analysis of a coral larval transcriptome using 454 gsflx |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689275/ https://www.ncbi.nlm.nih.gov/pubmed/19435504 http://dx.doi.org/10.1186/1471-2164-10-219 |
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