Literature DB >> 34189264

The complete chloroplast genome sequence of Sapindus delavayi, a species endemic to China.

Xuyang Wang1, Lianchun Wang1, Huimin Liu1, Dawei Wang1, Qing Li2.   

Abstract

Sapindus delavayi, widely distributed in central to southwest of China, is an economically important forest tree. The chloroplast genome is 159,861 bp in length with a typical circular quadripartite structure, containing 129 genes (84 protein-coding genes, 37 tRNAs, and eight rRNAs). Our phylogenetic result clearly showed that S. delavayi and S. mukorossi have the closest relationship.
© 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Sapindus delavayi; chloroplast genome; phylogenetic analysis

Year:  2021        PMID: 34189264      PMCID: PMC8208118          DOI: 10.1080/23802359.2021.1935338

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.658


Sapindus delavayi (Franch.) Radlk., commonly known as the soap fruit, belonging to the Sapindaceae family, is widely distributed in central to southwest of China (Sun, Jia, et al. 2017; Sun, Wang, et al. 2017). The pericarp of S. delavayi is rich in polyphenols and saponins, and the saponins can be used as a highly effective natural surfactant in commercial productions (Nakayama et al. 1986). The S. delavayi saponins are also used to expel parasite, suppress coughing, and treat inflammation (Quetin-Leclercq et al. 1992; Zhou et al. 2010; Zhou et al. 2013; Wu et al. 2013; Xu et al. 2013). It is reported that the seed oils produced by S. delavayi are rich in medium-chain monounsaturated fatty acids and suitable to produce biodiesel (Sun et al. 2018). The root and fruit of S. delavayi are commonly used as traditional Chinese medicine, and the trunk of the plant is used as wood to make box boards and combs (Xu et al. 2013). As a wild resource, S. delavayi is limited in its development and utilization due to the lack of genetic information (Zeng et al. 2018). To restore the S. delavayi forest and make better use of it, it is necessary to protect the existing wild S. delavayi and have a deeper understanding of its phylogenetic relationships with other Sapindaceae species. Chloroplast genome sequences have been widely used to reconstruct phylogenetic relationships and explore the structural and functional evolution (Jansen et al. 2007; Moore et al. 2010; Wang et al. 2020). In our study, the complete chloroplast genome of S. delavayi was assembled and annotated for the first time. The study provides a basis for the relationship between several main clades of the Sapindaceae family. The leaves of S. delavayi were collected from Nanjian, Yunnan, China (100°24′′08′′E, 24°54′70′′N, 1132 m), in August 2020. Total genome DNA was extracted and sequenced by Annoroad Gene Technology (Beijing, China). The original specimen of this species was stored in the herbarium of Southwest Forestry University with accession number: SWFU-YAB-H-0330. Total DNA was sequenced using the Illumina Novaseq 6000 platform at Annoroad Gene Technology (Beijing, China). About 4.51 GB of high-quality clean reads were generated by 150 bp paired read length. The complete cp genome of S. delavayi was assembled with GetOrganelle version 1.6.2 (Jin et al. 2020) (The parameters of GetOrganelle version 1.6.2 are as follows: Cycles: 15; KMER value: 21, 45, 65, 85, and 105; The chloroplast genome database name used for assembly: EMBPLANT_PT). Genome annotation of S. delavayi was performed by employing the program Geneious R8 and manually adjusted by comparing it to the reference genome S. mukorossi. The chloroplast DNA sequence was deposited at the GenBank database with the accession number MW041255. The complete cp genome of S. delavayi was 159,861 bp long in length. It contained SSC of 18,657 bp add of and LSC of 85,242 bp, separated by a pair of inverted repeats (IRa and IRb, 27,981 bp), showed a typical angiosperm quadripartite structure. The GC contents of the four regions above were 31.6%, 35.8%, 42.6%, and 42.6%, respectively. The whole cp genome included functional 129 genes (eight rRNA, 37 tRNA, and 84 protein-coding genes). Three genes (rps12, ycf3, and clpP) had two introns and 17 genes (rpl2, ndhB, trnI-GAU, trnA-UGC, ndhA, trnI-GAU, ndhB, petB, trnV-UAC, trnL-UAA, rpoC1, atpF, trnG-GCC, rps16, and trnK-UUU) had only one intron. We constructed a phylogenetic tree with the cp genomes of S. delavayi and other 17 species to analyze the phylogenetic relationship of S. delavayi with species in the Sapindaceae family (the species Anacardium occidentale were set as outgroup). MEGA version 7.0 was applied to align the 18 complete chloroplast sequences (Kumar et al. 2016). With the Maximum-likelihood method, the model ‘K3Pu + F+R3’ was chosen to be the best nucleotide substitution model in IQ-tree version 1.5.5 (Nguyen et al. 2015) (Figure 1). Five Acer species and Dipteronia sinensis, Dipteronia dyeriana, and Aesculus wangii formed a cluster (BS = 100). Another cluster (BS = 100) contained eight species (including the cp genome newly sequenced in this study): Dimocarpus longan, Litchi chinensisPometia tomentosa, Sapindus mukorossi, Sapindus delavayi, Koelreuteria paniculata, Dodonaea viscosa, Euonymus hamiltonianus. Anacardium occidentale, and Mangifera indica were using as outgroup. Within the tribe Sapindus, S. delavayi had close relationship with S. mukorossi. The analysis provided essential molecular information for S. delavayi and reference for the systematic differentiation of Sapindaceae.
Figure 1.

The phylogramf is based on the complete chloroplast genome sequences of Sapindus delavayi and other 17 species.

The phylogramf is based on the complete chloroplast genome sequences of Sapindus delavayi and other 17 species.
  7 in total

1.  Cytotoxic activity of some triterpenoid saponins.

Authors:  J Quetin-Leclercq; R Elias; G Balansard; R Bassleer; L Angenot
Journal:  Planta Med       Date:  1992-06       Impact factor: 3.352

2.  Phylogenetic analysis of 83 plastid genes further resolves the early diversification of eudicots.

Authors:  Michael J Moore; Pamela S Soltis; Charles D Bell; J Gordon Burleigh; Douglas E Soltis
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-22       Impact factor: 11.205

3.  MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets.

Authors:  Sudhir Kumar; Glen Stecher; Koichiro Tamura
Journal:  Mol Biol Evol       Date:  2016-03-22       Impact factor: 16.240

4.  Saponins of pericarps of Chinese Sapindus delavayi (Pyi-shiau-tzu), a source of natural surfactants.

Authors:  K Nakayama; H Fujino; R Kasai; O Tanaka; J Zhou
Journal:  Chem Pharm Bull (Tokyo)       Date:  1986-05       Impact factor: 1.645

5.  Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns.

Authors:  Robert K Jansen; Zhengqiu Cai; Linda A Raubeson; Henry Daniell; Claude W Depamphilis; James Leebens-Mack; Kai F Müller; Mary Guisinger-Bellian; Rosemarie C Haberle; Anne K Hansen; Timothy W Chumley; Seung-Bum Lee; Rhiannon Peery; Joel R McNeal; Jennifer V Kuehl; Jeffrey L Boore
Journal:  Proc Natl Acad Sci U S A       Date:  2007-11-28       Impact factor: 11.205

6.  IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies.

Authors:  Lam-Tung Nguyen; Heiko A Schmidt; Arndt von Haeseler; Bui Quang Minh
Journal:  Mol Biol Evol       Date:  2014-11-03       Impact factor: 16.240

7.  GetOrganelle: a fast and versatile toolkit for accurate de novo assembly of organelle genomes.

Authors:  Jian-Jun Jin; Wen-Bin Yu; Jun-Bo Yang; Yu Song; Claude W dePamphilis; Ting-Shuang Yi; De-Zhu Li
Journal:  Genome Biol       Date:  2020-09-10       Impact factor: 13.583

  7 in total

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