A pangenome insight into the genome divergence and flower color diversity among Rhododendron speciesShow others and affiliations
2026 (English)In: BMC Genomics, E-ISSN 1471-2164, Vol. 27, no 1, article id 101
Article in journal (Refereed) Published
Abstract [en]
Background: The Rhododendron genus (Rhododendron L.), recognized as the most extensive woody plant genus in the Northern Hemisphere, captivates with its strikingly beautiful corollas and variety of flower colors. In addition, the Rhododendron genus exhibits a complex evolutionary history and substantial species diversification. To comprehensively understand the genomic complexity and flower color diversity within this genus, comparative genomics has emerged as a promising approach, enabling analysis at a super-species level.
Results: Here, we collected whole-genome data from seven rhododendrons of different subgenera to investigate the patterns of interspecific genomic and sequence divergence, as well as evolutionary dynamics of gene family related to flower color. We discovered that approximately 50% of Rhododendron genomes are composed of transposable elements (TEs), with over half of them being long terminal repeat retrotransposons (LTR-RTs). TEs significantly associate with genomic differentiation and structural variances within the genus. Additionally, the duplication and loss of genes associated with flower color and their corresponding expression over time are potentially driven by TEs.
Conclusion: Our comparative genomic analysis accentuates the critical role of TEs in genome divergence within the Rhododendron genus, highlighting their potential role as a key factor governing speciation and interspecific variability within the genus.
Place, publisher, year, edition, pages
BioMed Central (BMC), 2026. Vol. 27, no 1, article id 101
Keywords [en]
Flower color, Gene duplication, Gene loss, Rhododendron, Transposable element
National Category
Genetics and Genomics
Identifiers
URN: urn:nbn:se:umu:diva-249670DOI: 10.1186/s12864-025-12461-5ISI: 001672354300001PubMedID: 41495655Scopus ID: 2-s2.0-105028677764OAI: oai:DiVA.org:umu-249670DiVA, id: diva2:2037983
2026-02-122026-02-122026-02-12Bibliographically approved