Usability of reference-free transcriptome assemblies for detection of differential expression: a case study on Aethionema arabicum dimorphic seeds
Jazyk angličtina Země Anglie, Velká Británie Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
RE 1697/8-1
Deutsche Forschungsgemeinschaft
849.13.004
Netherlands Organization for International Cooperation in Higher Education
BB/M00192X/1 BB/M000583/1
Biotechnology and Biological Sciences Research Council - United Kingdom
NE/L002485/1
Natural Environment Research Council
PubMed
30700268
PubMed Central
PMC6354389
DOI
10.1186/s12864-019-5452-4
PII: 10.1186/s12864-019-5452-4
Knihovny.cz E-zdroje
- Klíčová slova
- Aethionema arabicum, Dimorphic seeds, RNA-seq, Reference and reference-free, Transcriptome,
- MeSH
- anotace sekvence MeSH
- Brassicaceae genetika růst a vývoj MeSH
- genom rostlinný MeSH
- genová ontologie MeSH
- klíčení MeSH
- regulace genové exprese u rostlin * MeSH
- rostlinné proteiny genetika MeSH
- semena rostlinná genetika růst a vývoj MeSH
- stanovení celkové genové exprese MeSH
- transkriptom * MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- rostlinné proteiny MeSH
BACKGROUND: RNA-sequencing analysis is increasingly utilized to study gene expression in non-model organisms without sequenced genomes. Aethionema arabicum (Brassicaceae) exhibits seed dimorphism as a bet-hedging strategy - producing both a less dormant mucilaginous (M+) seed morph and a more dormant non-mucilaginous (NM) seed morph. Here, we compared de novo and reference-genome based transcriptome assemblies to investigate Ae. arabicum seed dimorphism and to evaluate the reference-free versus -dependent approach for identifying differentially expressed genes (DEGs). RESULTS: A de novo transcriptome assembly was generated using sequences from M+ and NM Ae. arabicum dry seed morphs. The transcripts of the de novo assembly contained 63.1% complete Benchmarking Universal Single-Copy Orthologs (BUSCO) compared to 90.9% for the transcripts of the reference genome. DEG detection used the strict consensus of three methods (DESeq2, edgeR and NOISeq). Only 37% of 1533 differentially expressed de novo assembled transcripts paired with 1876 genome-derived DEGs. Gene Ontology (GO) terms distinguished the seed morphs: the terms translation and nucleosome assembly were overrepresented in DEGs higher in abundance in M+ dry seeds, whereas terms related to mRNA processing and transcription were overrepresented in DEGs higher in abundance in NM dry seeds. DEGs amongst these GO terms included ribosomal proteins and histones (higher in M+), RNA polymerase II subunits and related transcription and elongation factors (higher in NM). Expression of the inferred DEGs and other genes associated with seed maturation (e.g. those encoding late embryogenesis abundant proteins and transcription factors regulating seed development and maturation such as ABI3, FUS3, LEC1 and WRI1 homologs) were put in context with Arabidopsis thaliana seed maturation and indicated that M+ seeds may desiccate and mature faster than NM. The 1901 transcriptomic DEG set GO-terms had almost 90% overlap with the 2191 genome-derived DEG GO-terms. CONCLUSIONS: Whilst there was only modest overlap of DEGs identified in reference-free versus -dependent approaches, the resulting GO analysis was concordant in both approaches. The identified differences in dry seed transcriptomes suggest mechanisms underpinning previously identified contrasts between morphology and germination behaviour of M+ and NM seeds.
BIOSS Centre for Biological Signalling Studies University of Freiburg Freiburg Germany
Biosystematics Group Wageningen University Wageningen 6708 PB The Netherlands
Department of Horticulture Michigan State University East Lansing MI 48864 USA
Division of Biological Sciences University of Missouri Columbia MO 65211 USA
Plant Cell Biology Faculty of Biology University of Marburg 35043 Marburg Germany
School of Biological Sciences Royal Holloway University of London Egham Surrey TW20 0EX UK
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