Abstract

The genus Blumea (Asteroideae, Asteraceae) comprises about 100 species, including herbs, shrubs, and small trees. Previous studies have been unable to resolve taxonomic issues and the phylogeny of the genus Blumea due to the low polymorphism of molecular markers. Therefore, suitable polymorphic regions need to be identified. Here, we de novo assembled plastomes of the three Blumea species B. oxyodonta, B. tenella, and B. balsamifera and compared them with 26 other species of Asteroideae after correction of annotations. These species have quadripartite plastomes with similar gene content, genome organization, and inverted repeat contraction and expansion comprising 113 genes, including 80 protein‐coding, 29 transfer RNA, and 4 ribosomal RNA genes. The comparative analysis of codon usage, amino acid frequency, microsatellite repeats, oligonucleotide repeats, and transition and transversion substitutions has revealed high resemblance among the newly assembled species of Blumea. We identified 10 highly polymorphic regions with nucleotide diversity above 0.02, including rps16‐trnQ, ycf1, ndhF‐rpl32, petN‐psbM, and rpl32‐trnL, and they may be suitable for the development of robust, authentic, and cost‐effective markers for barcoding and inference of the phylogeny of the genus Blumea. Among these highly polymorphic regions, five regions also co‐occurred with oligonucleotide repeats and support use of repeats as a proxy for the identification of polymorphic loci. The phylogenetic analysis revealed a close relationship between Blumea and Pluchea within the tribe Inuleae. At tribe level, our phylogeny supports a sister relationship between Astereae and Anthemideae rooted as Gnaphalieae, Calenduleae, and Senecioneae. These results are contradictory to recent studies which reported a sister relationship between “Senecioneae and Anthemideae” and “Astereae and Gnaphalieae” or a sister relationship between Astereae and Gnaphalieae rooted as Calenduleae, Anthemideae, and then Senecioneae using nuclear genome sequences. The conflicting phylogenetic signals observed at the tribal level between plastidt and nuclear genome data require further investigation.

Highlights

  • The plastome has a mostly quadripartite structure in which a pair of inverted repeats (IRa and IRb) separate large single-­copy (LSC) and small single-­copy (SSC) regions (Daniell et al, 2016; Henriquez et al, 2020a, 2020b)

  • We de novo assembled the plastomes of three Blumea species and compared them with 26 other Asteroideae species

  • We provided insight into plastome structure, IR contraction and expansion, and suitable polymorphic loci

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Summary

| INTRODUCTION

The plastome has a mostly quadripartite structure in which a pair of inverted repeats (IRa and IRb) separate large single-­copy (LSC) and small single-­copy (SSC) regions (Daniell et al, 2016; Henriquez et al, 2020a, 2020b). Asteroideae is the recently diverged, ~37 mya (Mandel et al, 2019) or ~45 mya (Panero & Crozier, 2016), subfamily of Asteraceae and is divided into three super tribes, including Helianthodae (6,611 species), Senecionadae (3,480), and Asterodae (7,109) (Panero & Crozier, 2016). We are interested in (a) providing new insight into the plastome of the genus Blumea and performing comparative plastid genomics with other species of the subfamily Asteroideae; (b) reconstructing the phylogeny within the subfamily Asteroideae; (c) identifying suitable polymorphic loci for the phylogenetic inference of the genus Blumea; (d) elucidating the role of repeats as a proxy for the identification of mutational hot spots

| MATERIALS AND METHODS
Findings
| DISCUSSION
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