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Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2019 Oct 24;4(2):3766–3767. doi: 10.1080/23802359.2019.1681322

The complete plastid genome sequence of Begonia guangxiensis

Li-Na Dong a,, Xin-Yu Du b, Wei Zhou b
PMCID: PMC7707394  PMID: 33366181

Abstract

Begonia guangxiensis was assessed as endangered according to Red List of Chinese Plants. In this study, we described the complete plastid genome of B. guangxiensis. The plastid genome sequence of B. guangxiensis is 157,648 bp in size, having a large single-copy region (LSC) of 86,514 bp, a small single-copy region (SSC) of 18,076 bp, and two inverted repeat (IR) regions of 26,529 bp. The complete plastid genome of B. guangxiensis encoding 112 unique genes including 79 protein-coding genes, 29 tRNA genes, and four rRNA genes. The overall GC content of the plastid genome is 35.9%. Phylogenetic analysis confirmed that B. guangxiensis is closely related to B. varipeltata.

Keywords: Begonia guangxiensis, Begoniaceae, plastid genome


Begonia guangxiensis C.Y. Wu belongs to sect. Coelocentrum in the genera Begonia L. of the family Begoniaceae. This species was assessed as endangered according to Red List of Chinese Plants (Qin et al. 2013) and endemic to limestone area in Guangxi of China (Wu and Ku 1997). Because of the destruction of habitats and over-collection, the species is facing serious threat. Thus, we reported the plastid genome sequences of B. guangxiensis, which will contribute to conservation and further study of this species

Total DNA was extracted from fresh leaves of a single individual of B. guangxiensis in greenhouse (102°44′40.9″E, 25°08′06.3″N), which is cultivated in Kunming Institute of Botany, Chinese Academy of Sciences. The voucher specimen of B. guangxiensis was stored at Guangxi Institute of Botany (IBK 00418686).

Illumina paired-end (PE) library of ca. 500 bp was constructed and sequenced with ca. 200 bp PE read length, following the standard protocols on the Illumina HiSeq 2500 platform in Kunming Institute of Botany in Kunming, China. Approximately 2.0 Gb of clean data were obtained. De novo assemblies were constructed with SPAdes 3.9.1 (Bankevich et al. 2012). GetOrganelle (Jin et al. 2018) was also used to improve accuracy and efficiency in de novo assembly. Reference-guided connecting and annotation were subsequently conducted using Bandage 0.8.1(Wick et al. 2015) and Geneious 9.1.4 (Kearse et al. 2012), based on previously published plastomes.

The assembled plastid genome of B. guangxiensis is 157,648 bp in length (MN480848). The plastid genome shows a typical quadripartite structure with one large single copy region (LSC) of 86,514 bp, one small single copy region (SSC) of 18,076 bp and a pair of inverted repeat regions (IRs) of 26,529 bp. There was a small gap between psbD gene and trnE-UUC gene within LSC, mainly due to multiple mononucleotide repeats. A total of 112 unique genes were encoded by the plastid genome, which including 79 protein-coding genes, four ribosomal RNA genes and 29 transfer RNA genes. The overall GC content of the plastid genome is 35.9% and coding sequences (CDS) amounted to 49.8% in size (78,504 bp).

The phylogenetic analysis was performed with additional 16 plastid genomes of the genera Begonia available on Dryad (Harrison et al. 2016) using W-IQ-TREE (Trifinopoulos et al. 2016). The result showed that B. guangxiensis is closely related to B. varipeltata (Figure 1).

Figure 1.

Figure 1.

The phylogenetic relationship of Begonia guangxiensis that reconstructed with 17 complete plastid genome sequences of Begonia.

Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

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