RESUMEN
The Cytisus-Genista complex includes species that have become invasive following introduction into new geographic ranges as ornamental shrubs. Despite their impacts, the evolutionary relationships among invasives, ornamentals, and native-range species have never been investigated. Our objective was to examine relationships within the Cytisus-Genista complex to determine (1) the taxonomic identity of invasive "French broom" and ornamental "sweet broom" and (2) whether "sweet broom" contributes to "French broom" populations directly or via hybridization. We used sequence data from chloroplast and nuclear regions to gain insight into evolutionary origins and to confirm taxonomic status. Our phylogenetic analyses suggest a complex evolutionary history that includes hybridization events. Placement of invasive and ornamental individuals within the Cytisus-Genista complex resolves taxonomic uncertainty in these groups, as our phylogenetic analyses recovered separate "French broom" and "sweet broom" clades within the G. monspessulana clade in the genus Genista. Extensive cloning and sequencing of the ITS region revealed that, although the majority of invasive "French broom" in California is Genista monspessulana, hybridization with individuals from the ornamental "sweet broom" clade likely occurs in populations throughout the state.
Asunto(s)
Cytisus/genética , Genista/genética , Especies Introducidas , Filogenia , Teorema de Bayes , California , Núcleo Celular/genética , Clonación Molecular , ADN de Cloroplastos/genética , ADN Intergénico/genética , Geografía , Hibridación Genética , Funciones de Verosimilitud , Datos de Secuencia MolecularRESUMEN
The high-resolution amplified fragment length polymorphism technique (AFLP), with single PstI restriction endonuclease and two selective primers (PstI-G and PstI-GC), was used for genomotyping and study of the genomic relationships between Genista tinctoria microsymbionts sampled in England, Poland, and Ukraine. Out of 906 amplification products obtained with both selective primers, 537 markers were polymorphic and could be used to differentiate studied nodule isolates. Cluster analysis, based on AFLP patterns from PCR reaction with PstI-G and PstI-GC primers, separated Genista tinctoria rhizobia into three subgroups according to their geographic origin. The results presented in this paper emphasize the role of AFLP analysis in taxonomic and ecological studies of rhizobia.