Abstract
Prunus davidiana (Rosaceae) is of great importance horticulturally as the rootstock of some fruit trees. Here, the complete chloroplast genome of P. davidiana was assembled based on the Illumina reads. The complete cp genome of P. davidiana was 157,660 bp in length and contained a pair of inverted repeat (IR, 26,387 bp) regions, which were separated by the small single-copy (SSC, 19,122 bp) and the large single-copy (LSC, 85,764 bp) regions. It encoded 135 genes. The phylogenetic analysis revealed that P. davidiana is sister to other peaches. This result will be useful for future studies of the lineage.
Keywords: Chloroplast genome, Prunus davidiana, phylogenetic analysis
Prunus davidiana (Carriére) de Vos ex L. Henry (Rosaceae) is always used as the rootstock of fruit trees such as peach, plum in China, and also as an ornamental plant with attractive pink flowers, showing a great horticultural value (Lu 1986). Here, the chloroplast (cp) genome of P. davidiana was assembled by using the genome skimming approach (Zimmer and Wen 2015). It will be useful for future studies on the taxonomy and phylogeny of the economically important peach lineage of Prunus (Zhao et al. 2016).
Prunus davidiana was sampled from Mt. Taibaishan, Meixian County, China (107°40′34′′E, 34°02′33′′N, alt. 945 m). A voucher specimen (LMR20160501) was deposited in the Herbarium of Northwest A&F University (WUK), China. Total genomic DNA was extracted with the modified cetyltrimethylammonium bromide (CTAB) method (Doyle and Doyle 1987). The extracted DNA was sequenced using the Illumina Miseq platform (Illumina, San Diego, CA). Reads of the cp genome were assembled using GetOrganelle (Jin et al. 2018). The annotation of the cp genome sequence was performed using PGA (https://github.com/quxiaojian/PGA). The genome map was generated in the webserver OGDRAW (http://ogdraw.mpimp-golm.mpg.de) (Lohse et al. 2013). The annotated complete cp genome sequence was submitted to GenBank (Accession Number MK634746).
The complete cp genome of P. davidiana was 157,660 bp in length and contained a pair of inverted repeat (IR, 26,387 bp) regions, which were separated by a small single-copy (SSC, 19,122 bp) region and a large single-copy (LSC, 85,764 bp) region. The whole cp genome encoded 135 genes including 88 protein-coding genes (PCG), 39 tRNA genes, 8 rRNA genes. Of these genes, 16 genes (atpF, ndhA, ndhB, petB, petD, rpl2, rpl16, rpoC1, rps12, rps16, trnA-UGC, trnI-GAU, trnG-UCC, trnK-UUU, trnL-UAA, and trnV-UAC) had one intron and 2 genes (clpP and ycf3) had two introns. Most genes occurred in a single copy, while six PCGs (ndhB, rpl2, rpl23, rps7, rps12, and ycf2), seven tRNA genes (trnA-UGC, trnI-CAU, trnI-GAU, trnL-CAA, trnN-GUU, trnR-ACG, and trnV-GAC), and four rRNA genes (rrn4.5, rrn5, rrn16, and rrn23) in IR regions are duplicated. The overall GC content of P. davidiana cp genome is 36.8% with 34.6, 30.3, and 42.6% GC in the LSC, SSC, and IR regions, respectively.
Totally 12 additional cp genomes of the genus Prunus L. were used to obtain the phylogenetic position of P. davidiana. Prinsepia utilis and Prinsepia sinensis were used as the outgroup. All the cp genome sequences were aligned in MAFFT (Katoh and Standley 2013), which was implemented in Geneious R10 (Biomatters Ltd., Auckland, New Zealand). We reconstructed a phylogeny under the maximum-likelihood criterion in RAxML (Stamatakis 2014) and determined the clade support using 10,000 bootstrap replicates. The phylogenetic tree shows that P. davidiana and other species of subgenus Amygdalus form a small clade (Figure 1), which is consistent with the prior phylogenetic studies of Prunus based on several molecular markers (Bortiri et al. 2001; Wen et al. 2008; Zhao et al. 2016). We expect that the cp genome of P. davidiana will be valuable for future horticultural studies.
Figure 1.
Maximum-likelihood phylogenetic tree for genus Prunus L. based on 14 complete chloroplast genomes. The number on each node indicates bootstrap support value >50% for each clade. Accession Numbers: Prunus kansuensis (KF990036), Prunus davidiana (MK634746), P. persica (HQ336405), Prunus mongolica (MG602256), Prunus armeniaca (KY420025), Prunus pedunculata (MG602257), Prunus salicina (KY420002), Prunus yedoensis (KU985054), Prunus conradinae (KY419991), Prunus pseudocerasus (KX255667), Prunus undulata (KY420035), Prinsepia utilis (KC571835), Prinsepia sinensis (KY419985).
Funding Statement
This work was supported by the National Natural Science Foundation of China [31770200].
Disclosure statement
No potential conflict of interest was reported by the authors.
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