Cargando…

Gene Expression Changes During the Allo-/Deallopolyploidization Process of Brassica napus

Gene expression changes due to allopolyploidization have been extensively studied in plants over the past few decades. Nearly all these studies focused on comparing the changes before and after genome merger. In this study, we used the uniquely restituted Brassica rapa (RBR, A(e)A(e), 2n = 20) obtai...

Descripción completa

Detalles Bibliográficos
Autores principales: Pan, Qi, Zhu, Bin, Zhang, Dawei, Tong, Chaobo, Ge, Xianhong, Liu, Shengyi, Li, Zaiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931035/
https://www.ncbi.nlm.nih.gov/pubmed/31921314
http://dx.doi.org/10.3389/fgene.2019.01279
Descripción
Sumario:Gene expression changes due to allopolyploidization have been extensively studied in plants over the past few decades. Nearly all these studies focused on comparing the changes before and after genome merger. In this study, we used the uniquely restituted Brassica rapa (RBR, A(e)A(e), 2n = 20) obtained from Brassica napus (A(n)A(n)C(n)C(n), 2n = 38) to analyze the gene expression changes and its potential mechanism during the process of allo-/deallopolyploidization. RNA-seq-based transcriptome profiling identified a large number of differentially expressed genes (DEGs) between RBR and natural B. rapa (A(r)A(r)), suggesting potential effects of allopolyploidization/domestication of AA component of B. napus at the tetrapolyploid level. Meanwhile, it was revealed that up to 20% of gene expressions were immediately altered when compared with those in the A(n)-subgenome. Interestingly, one fifth of these changes are in fact indicative of the recovery of antecedent gene expression alternations occurring since the origin of B. napus and showed association with homoeologous expression bias between A(n) and C(n) subgenomes. Enrichment of distinct gene ontology (GO) categories of the above sets of genes further indicated potential functional cooperation of the A(n) and C(n) subgenome of B. napus. Whole genome methylation analysis revealed a small number of DEGs were identified in the differentially methylated regions.