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The draft genome and transcriptome of Cannabis sativa
BACKGROUND: Cannabis sativa has been cultivated throughout human history as a source of fiber, oil and food, and for its medicinal and intoxicating properties. Selective breeding has produced cannabis plants for specific uses, including high-potency marijuana strains and hemp cultivars for fiber and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359589/ https://www.ncbi.nlm.nih.gov/pubmed/22014239 http://dx.doi.org/10.1186/gb-2011-12-10-r102 |
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author | van Bakel, Harm Stout, Jake M Cote, Atina G Tallon, Carling M Sharpe, Andrew G Hughes, Timothy R Page, Jonathan E |
author_facet | van Bakel, Harm Stout, Jake M Cote, Atina G Tallon, Carling M Sharpe, Andrew G Hughes, Timothy R Page, Jonathan E |
author_sort | van Bakel, Harm |
collection | PubMed |
description | BACKGROUND: Cannabis sativa has been cultivated throughout human history as a source of fiber, oil and food, and for its medicinal and intoxicating properties. Selective breeding has produced cannabis plants for specific uses, including high-potency marijuana strains and hemp cultivars for fiber and seed production. The molecular biology underlying cannabinoid biosynthesis and other traits of interest is largely unexplored. RESULTS: We sequenced genomic DNA and RNA from the marijuana strain Purple Kush using shortread approaches. We report a draft haploid genome sequence of 534 Mb and a transcriptome of 30,000 genes. Comparison of the transcriptome of Purple Kush with that of the hemp cultivar 'Finola' revealed that many genes encoding proteins involved in cannabinoid and precursor pathways are more highly expressed in Purple Kush than in 'Finola'. The exclusive occurrence of Δ(9)-tetrahydrocannabinolic acid synthase in the Purple Kush transcriptome, and its replacement by cannabidiolic acid synthase in 'Finola', may explain why the psychoactive cannabinoid Δ(9)-tetrahydrocannabinol (THC) is produced in marijuana but not in hemp. Resequencing the hemp cultivars 'Finola' and 'USO-31' showed little difference in gene copy numbers of cannabinoid pathway enzymes. However, single nucleotide variant analysis uncovered a relatively high level of variation among four cannabis types, and supported a separation of marijuana and hemp. CONCLUSIONS: The availability of the Cannabis sativa genome enables the study of a multifunctional plant that occupies a unique role in human culture. Its availability will aid the development of therapeutic marijuana strains with tailored cannabinoid profiles and provide a basis for the breeding of hemp with improved agronomic characteristics. |
format | Online Article Text |
id | pubmed-3359589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-33595892012-05-25 The draft genome and transcriptome of Cannabis sativa van Bakel, Harm Stout, Jake M Cote, Atina G Tallon, Carling M Sharpe, Andrew G Hughes, Timothy R Page, Jonathan E Genome Biol Research BACKGROUND: Cannabis sativa has been cultivated throughout human history as a source of fiber, oil and food, and for its medicinal and intoxicating properties. Selective breeding has produced cannabis plants for specific uses, including high-potency marijuana strains and hemp cultivars for fiber and seed production. The molecular biology underlying cannabinoid biosynthesis and other traits of interest is largely unexplored. RESULTS: We sequenced genomic DNA and RNA from the marijuana strain Purple Kush using shortread approaches. We report a draft haploid genome sequence of 534 Mb and a transcriptome of 30,000 genes. Comparison of the transcriptome of Purple Kush with that of the hemp cultivar 'Finola' revealed that many genes encoding proteins involved in cannabinoid and precursor pathways are more highly expressed in Purple Kush than in 'Finola'. The exclusive occurrence of Δ(9)-tetrahydrocannabinolic acid synthase in the Purple Kush transcriptome, and its replacement by cannabidiolic acid synthase in 'Finola', may explain why the psychoactive cannabinoid Δ(9)-tetrahydrocannabinol (THC) is produced in marijuana but not in hemp. Resequencing the hemp cultivars 'Finola' and 'USO-31' showed little difference in gene copy numbers of cannabinoid pathway enzymes. However, single nucleotide variant analysis uncovered a relatively high level of variation among four cannabis types, and supported a separation of marijuana and hemp. CONCLUSIONS: The availability of the Cannabis sativa genome enables the study of a multifunctional plant that occupies a unique role in human culture. Its availability will aid the development of therapeutic marijuana strains with tailored cannabinoid profiles and provide a basis for the breeding of hemp with improved agronomic characteristics. BioMed Central 2011 2011-10-20 /pmc/articles/PMC3359589/ /pubmed/22014239 http://dx.doi.org/10.1186/gb-2011-12-10-r102 Text en Copyright ©2011 van Bakel 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 van Bakel, Harm Stout, Jake M Cote, Atina G Tallon, Carling M Sharpe, Andrew G Hughes, Timothy R Page, Jonathan E The draft genome and transcriptome of Cannabis sativa |
title | The draft genome and transcriptome of Cannabis sativa |
title_full | The draft genome and transcriptome of Cannabis sativa |
title_fullStr | The draft genome and transcriptome of Cannabis sativa |
title_full_unstemmed | The draft genome and transcriptome of Cannabis sativa |
title_short | The draft genome and transcriptome of Cannabis sativa |
title_sort | draft genome and transcriptome of cannabis sativa |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359589/ https://www.ncbi.nlm.nih.gov/pubmed/22014239 http://dx.doi.org/10.1186/gb-2011-12-10-r102 |
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