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De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology

Rehmannia glutinosa is a potent medicinal plant with a significant importance in traditional Chinese medicine. Its root is enriched with various bioactive molecules mainly iridoids, possessing important pharmaceutical properties. However, the molecular biology and evolution of R. glutinosa have been...

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Autores principales: Ma, Ligang, Dong, Chengming, Song, Chi, Wang, Xiaolan, Zheng, Xiaoke, Niu, Yan, Chen, Shilin, Feng, Weisheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318827/
https://www.ncbi.nlm.nih.gov/pubmed/34377362
http://dx.doi.org/10.1016/j.csbj.2021.07.006
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author Ma, Ligang
Dong, Chengming
Song, Chi
Wang, Xiaolan
Zheng, Xiaoke
Niu, Yan
Chen, Shilin
Feng, Weisheng
author_facet Ma, Ligang
Dong, Chengming
Song, Chi
Wang, Xiaolan
Zheng, Xiaoke
Niu, Yan
Chen, Shilin
Feng, Weisheng
author_sort Ma, Ligang
collection PubMed
description Rehmannia glutinosa is a potent medicinal plant with a significant importance in traditional Chinese medicine. Its root is enriched with various bioactive molecules mainly iridoids, possessing important pharmaceutical properties. However, the molecular biology and evolution of R. glutinosa have been largely unexplored. Here, we report a reference genome of R. glutinosa using Nanopore technology, Illumina and Hi-C sequencing. The assembly genome is 2.49 Gb long with a scaffold N50 length of 70 Mb and high heterozygosity (2%). Since R. glutinosa is an autotetraploid (4n = 56), the difference between each set of chromosomes is very small, and it is difficult to distinguish the two sets of chromosomes using Hi-C. Hence, only one set of the genome size was mounted to the chromosome level. Scaffolds covering 52.61% of the assembled genome were anchored on 14 pseudochromosomes. Over 67% of the genome consists of repetitive sequences dominated by Copia long terminal repeats and 48,475 protein-coding genes were predicted. Phylogenetic analysis corroborates the placement of R. glutinosa in the Orobanchaceae family. Our results indicated an independent and very recent whole genome duplication event that occurred 3.64 million year ago in the R. glutinosa lineage. Comparative genomics analysis demonstrated expansion of the UDP-dependent glycosyltransferases and terpene synthase gene families, known to be involved in terpenoid biosynthesis and diversification. Furthermore, the molecular biosynthetic pathway of iridoids has been clarified in this work. Collectively, the generated reference genome of R. glutinosa will facilitate discovery and development of important pharmacological compounds.
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spelling pubmed-83188272021-08-09 De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology Ma, Ligang Dong, Chengming Song, Chi Wang, Xiaolan Zheng, Xiaoke Niu, Yan Chen, Shilin Feng, Weisheng Comput Struct Biotechnol J Research Article Rehmannia glutinosa is a potent medicinal plant with a significant importance in traditional Chinese medicine. Its root is enriched with various bioactive molecules mainly iridoids, possessing important pharmaceutical properties. However, the molecular biology and evolution of R. glutinosa have been largely unexplored. Here, we report a reference genome of R. glutinosa using Nanopore technology, Illumina and Hi-C sequencing. The assembly genome is 2.49 Gb long with a scaffold N50 length of 70 Mb and high heterozygosity (2%). Since R. glutinosa is an autotetraploid (4n = 56), the difference between each set of chromosomes is very small, and it is difficult to distinguish the two sets of chromosomes using Hi-C. Hence, only one set of the genome size was mounted to the chromosome level. Scaffolds covering 52.61% of the assembled genome were anchored on 14 pseudochromosomes. Over 67% of the genome consists of repetitive sequences dominated by Copia long terminal repeats and 48,475 protein-coding genes were predicted. Phylogenetic analysis corroborates the placement of R. glutinosa in the Orobanchaceae family. Our results indicated an independent and very recent whole genome duplication event that occurred 3.64 million year ago in the R. glutinosa lineage. Comparative genomics analysis demonstrated expansion of the UDP-dependent glycosyltransferases and terpene synthase gene families, known to be involved in terpenoid biosynthesis and diversification. Furthermore, the molecular biosynthetic pathway of iridoids has been clarified in this work. Collectively, the generated reference genome of R. glutinosa will facilitate discovery and development of important pharmacological compounds. Research Network of Computational and Structural Biotechnology 2021-07-08 /pmc/articles/PMC8318827/ /pubmed/34377362 http://dx.doi.org/10.1016/j.csbj.2021.07.006 Text en © 2021 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Ma, Ligang
Dong, Chengming
Song, Chi
Wang, Xiaolan
Zheng, Xiaoke
Niu, Yan
Chen, Shilin
Feng, Weisheng
De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology
title De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology
title_full De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology
title_fullStr De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology
title_full_unstemmed De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology
title_short De novo genome assembly of the potent medicinal plant Rehmannia glutinosa using nanopore technology
title_sort de novo genome assembly of the potent medicinal plant rehmannia glutinosa using nanopore technology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318827/
https://www.ncbi.nlm.nih.gov/pubmed/34377362
http://dx.doi.org/10.1016/j.csbj.2021.07.006
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