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De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation

Hidden underground, root systems constitute an important part of the plant for its development, nourishment and sensing the soil environment around it, but we know very little about its genetic regulation in crop plants like wheat. In the present study, we de novo assembled the root transcriptomes i...

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Autores principales: Challa, Ghana Shyam, Li, Wanlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218025/
https://www.ncbi.nlm.nih.gov/pubmed/30395610
http://dx.doi.org/10.1371/journal.pone.0205582
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author Challa, Ghana Shyam
Li, Wanlong
author_facet Challa, Ghana Shyam
Li, Wanlong
author_sort Challa, Ghana Shyam
collection PubMed
description Hidden underground, root systems constitute an important part of the plant for its development, nourishment and sensing the soil environment around it, but we know very little about its genetic regulation in crop plants like wheat. In the present study, we de novo assembled the root transcriptomes in reference cultivar Chinese Spring from RNA-seq reads generated by the 454-GS-FLX and HiSeq platforms. The FLX reads were assembled into 24,986 transcripts with completeness of 54.84%, and the HiSeq reads were assembled into 91,543 high-confidence protein-coding transcripts, 2,404 low-confidence protein-coding transcripts, and 13,181 non-coding transcripts with the completeness of >90%. Combining the FLX and HiSeq assemblies, we assembled a root transcriptome of 92,335 ORF-containing transcripts. Approximately 7% of the coding transcripts and ~2% non-coding transcripts are not present in the current wheat genome assembly. Functional annotation of both assemblies showed similar gene ontology patterns and that ~7% coding and >5% non-coding transcripts are root-specific. Transcription quantification identified 1,728 differentially expressed transcripts between root tips and maturation zone, and functional annotation of these transcripts captured a transcriptional signature of longitudinal development of wheat root. With the transcriptomic resources developed, this study provided the first view of wheat root transcriptome under different developmental zones and laid a foundation for molecular studies of wheat root development and growth using a reverse genetic approach.
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spelling pubmed-62180252018-11-19 De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation Challa, Ghana Shyam Li, Wanlong PLoS One Research Article Hidden underground, root systems constitute an important part of the plant for its development, nourishment and sensing the soil environment around it, but we know very little about its genetic regulation in crop plants like wheat. In the present study, we de novo assembled the root transcriptomes in reference cultivar Chinese Spring from RNA-seq reads generated by the 454-GS-FLX and HiSeq platforms. The FLX reads were assembled into 24,986 transcripts with completeness of 54.84%, and the HiSeq reads were assembled into 91,543 high-confidence protein-coding transcripts, 2,404 low-confidence protein-coding transcripts, and 13,181 non-coding transcripts with the completeness of >90%. Combining the FLX and HiSeq assemblies, we assembled a root transcriptome of 92,335 ORF-containing transcripts. Approximately 7% of the coding transcripts and ~2% non-coding transcripts are not present in the current wheat genome assembly. Functional annotation of both assemblies showed similar gene ontology patterns and that ~7% coding and >5% non-coding transcripts are root-specific. Transcription quantification identified 1,728 differentially expressed transcripts between root tips and maturation zone, and functional annotation of these transcripts captured a transcriptional signature of longitudinal development of wheat root. With the transcriptomic resources developed, this study provided the first view of wheat root transcriptome under different developmental zones and laid a foundation for molecular studies of wheat root development and growth using a reverse genetic approach. Public Library of Science 2018-11-05 /pmc/articles/PMC6218025/ /pubmed/30395610 http://dx.doi.org/10.1371/journal.pone.0205582 Text en © 2018 Challa, Li http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Challa, Ghana Shyam
Li, Wanlong
De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
title De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
title_full De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
title_fullStr De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
title_full_unstemmed De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
title_short De novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
title_sort de novo assembly of wheat root transcriptomes and transcriptional signature of longitudinal differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218025/
https://www.ncbi.nlm.nih.gov/pubmed/30395610
http://dx.doi.org/10.1371/journal.pone.0205582
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