Abstract

BackgroundAllopolyploids require rapid genetic and epigenetic modifications to reconcile two or more sets of divergent genomes. To better understand the fate of duplicate genes following genomic mergers and doubling during allopolyploid formation, in this study, we explored the global gene expression patterns in resynthesized allotetraploid Brassica napus (AACC) and its diploid parents B. rapa (AA) and B. oleracea (CC) using RNA sequencing of leaf transcriptomes.ResultsWe found that allopolyploid B. napus formation was accompanied by extensive changes (approximately one-third of the expressed genes) in the parental gene expression patterns (‘transcriptome shock’). Interestingly, the majority (85%) of differentially expressed genes (DEGs) were downregulated in the allotetraploid. Moreover, the homoeolog expression bias (relative contribution of homoeologs to the transcriptome) and expression level dominance (total expression level of both homoeologs) were thoroughly investigated by monitoring the expression of 23,766 B. oleracea-B. rapa orthologous gene pairs. Approximately 36.5% of the expressed gene pairs displayed expression bias with a slight preference toward the A-genome. In addition, 39.6, 4.9 and 9.0% of the expressed gene pairs exhibited expression level dominance (ELD), additivity expression and transgressive expression, respectively. The genome-wide ELD was also biased toward the A-genome in the resynthesized B. napus. To explain the ELD phenomenon, we compared the individual homoeolog expression levels relative to those of the diploid parents and found that ELD in the direction of the higher-expression parent can be explained by the downregulation of homoeologs from the dominant parent or upregulation of homoeologs from the nondominant parent; however, ELD in the direction of the lower-expression parent can be explained only by the downregulation of the nondominant parent or both homoeologs. Furthermore, Gene Ontology (GO) enrichment analysis suggested that the alteration in the gene expression patterns could be a prominent cause of the phenotypic variation between the newly formed B. napus and its parental species.ConclusionsCollectively, our data provide insight into the rapid repatterning of gene expression at the beginning of Brassica allopolyploidization and enhance our knowledge of allopolyploidization processes.

Highlights

  • Allopolyploids require rapid genetic and epigenetic modifications to reconcile two or more sets of divergent genomes

  • differentially expressed genes (DEGs) in nascent resynthesized B. napus To study the effects of allopolyploidization on gene expression in synthetic B. napus, we identified the DEGs between the synthetic B. napus (AACC) and its diploid parents (‘Yangzhouqing’, AA and ‘Yonglv 7’, CC)

  • We focused on the 39 significantly enriched biological process terms and found that most enriched Gene Ontology (GO) terms belonged to the Homoeolog expression bias in the resynthesized allotetraploid B. napus Many studies have shown that duplicate gene pairs may display homoeolog expression bias in allotetraploids in which bias refers to the preferential expression of one homoeolog relative to the other [5, 13, 41, 42]

Read more

Summary

Introduction

Allopolyploids require rapid genetic and epigenetic modifications to reconcile two or more sets of divergent genomes. Epigenetic changes, including DNA methylation, histone modification, transposon suppression/release and small RNA-mediated gene silencing, may occur at the transcriptional or posttranscriptional levels [4, 5, 7, 9,10,11,12]. The genetic and epigenetic changes in new allopolyploid genomes may lead to extensive gene expression [7, 10]. When two diverged genomes merge into a single cell, duplicate copies of genes with similar or redundant functions may alter their gene expression patterns, which takes several forms, including unequal parental contributions, transgressive upregulation or downregulation, silencing, and altered expression times and locations [4, 5, 13]. The alteration of gene expression patterns is a prominent cause of the phenotypic variation between newly formed allopolyploids and their parental species and may be the primary source of phenotypic novelty that may be selected and domesticated [4, 9]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call