Abstract
Jacaranda mimosifolia is a deciduous arbor with blue flowers native to Brazil, Bolivia, and Argentina in South America. After introduction from South America, it was widely cultivated as a garden ornamental plant in South China. The complete chloroplast (cp) genome sequence of this ornamental species is reported in this study, based on high-throughput sequencing (Illumina). The complete cp genome is 153,514 bp in length, containing a pair of inverted repeat regions (IRs) of 25,408 bp, a large single-copy (LSC) region of 84,755 bp, and a small single-copy (SSC) region of 17,943 bp. The cp genome contains 130 genes, consisting of 85 protein-coding genes, 37 tRNA genes, and 8 rRNA genes. The overall A/T content in the cp genome of J. mimosifolia is 61.70%. The phylogenetic analyses indicate that there is a close relationship between J. mimosifolia and Tecomaria capensis. The complete cp sequence of J. mimosifolia will provide a useful resource for the development and utilization of this species as well as for the phylogenetic studies in Bignoniaceae.
Keywords: Jacaranda mimosifolia, Illumina sequencing, complete chloroplast, phylogenetic analysis, Bignoniaceae
Jacaranda mimosifolia is a deciduous arbor belonging to the Jacaranda of Bignoniaceae, native to Brazil, Bolivia, and Argentina in South America. Its leaves are graceful and resemble Albizia julibrissin, the fruit is peculiar and resembles tortoise shell and the flowers are blue and bell-shaped. It is a very good ornamental plant for green, widely cultivated in Guangdong, Guangxi, Yunnan, and Hainan of China (Yang and Li 2011). Here, we report and characterize the complete chloroplast of J. mimosifolia (GenBank accession number: MN450152). This is the first report of a complete chloroplast for the J. mimosifolia.
We sampled a healthy individual of J. mimosifolia in this study from Baishamen Park, Haikou City (N20.07°, E110.33°). A voucher specimen (Wang et al., B263) was deposited in the Herbarium of the Institute of Tropical Agriculture and Forestry (HUTB), Hainan University, Haikou, China. We employed the modified CTAB method (Doyle and Doyle 1987) to extract the total genomic DNA of J. mimosifolia from silica gel-dried leaves.
Whole-genome short-gun sequencing was performed on the Illumina Hiseq 2500 platform (Illumina, San Diego, CA), with the 150 bp paired-end sequencing method. We carried out quality control of sequenced genomic data and cleaning up unqualified sequences (Patel and Jain 2012). Finally, about 6 GB of clean data is obtained. The J. mimosifolia was assembled by MITObim version 1.8 (omicX, France, Hahn et al. 2013). All genes were annotated by Geneious R version 8.0.2 (Biomatters Ltd., Auckland, New Zealand). The chloroplast genome of Erythranthe lutea (NC_030212.1) (Vallejo-Marín et al. 2016) was used as the reference for assembling and annotation. The annotation was corrected with DOGMA (Wyman et al. 2004).
The chloroplast genome of J. mimosifolia was a circular molecule of 153,514 bp with the typical quadripartite structure of angiosperms, containing two inverted repeats (IRs) of 25,408 bp, a large single-copy (LSC) region of 84,755 bp, a small single-copy (SSC) region of 17,943 bp. The chloroplast genome contains 130 genes, including 85 protein-coding genes, 37 tRNA genes, and 8 rRNA genes. The overall A/T content in the chloroplast genome of J. mimosifolia is 61.70%, which the corresponding value of the LSC, SSC, and IR region were 63.70%, 67.10%, and 56.60%, respectively.
A maximum-likelihood (ML) phylogenetic tree of the nine published complete chloroplast genomes of Bignoniaceae (plus J. mimosifolia) was built with RAxML (Stamatakis 2006), using Utricularia reniformis, Pinguicula ehlersiae, Salvia japonica, and Sesamum indicum as outgroups (Figure 1). The phylogenetic analysis indicated that all members of Bignoniaceae were clustered with a high bootstrap support (BS) value and there was a close relationship between J. mimosifolia and Tecomaria capensis. In this study, we report the characterization of the complete chloroplast genome of J. mimosifolia for the first time, which may provide a useful resource for development and utilization of J. mimosifolia, and also for phylogenetic studies of Bignoniaceae.
Figure 1.
The best ML phylogeny recovered from 13 complete plastome sequences by RAxML. Accession numbers: Jacaranda mimosifolia (this study, GenBank accession number: MN450152), Adenocalymma trifoliatum NC_037459.1, Anemopaegma glaucum NC_037231.1, Anemopaegma oligoneuron NC_037232.1, Dolichandra cynanchoides NC_037460.1, Neojobertia candolleana NC_036503.1, Pleonotoma albiflora NC_037461.1, Tanaecium tetragonolobum NC_027955.1, Tecomaria capensis NC_037462.1; Outgroups: Pinguicula ehlersiae NC_023463.1, Utricularia reniformis NC_029719.2, Salvia japonica KY646163.1, and Sesamum indicum KC569603.1.
Disclosure statement
No potential conflict of interest was reported by the authors.
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