Abstract
Peganum nigellastrum is a medicinal plant. The total chloroplast (cp) genome length of P. nigellastrum is 160,066 bp, Containing a large single copy region of 88,275 bp, two inverted repeat regions of 26,486 bp and a small single copy region of 18,855 bp. The chloroplast genome contains 132 complete genes, including 87 protein-coding genes (87 PCGs), 8 ribosomal RNA genes (8 rRNAs), and 37 tRNA genes (37 tRNAs). The overall GC content of cp DNA is 37.5%, the corresponding values of the LSC, SSC, and IR regions are 35.6%, 31.4%, and 42.8%. Phylogenetic tree shows that P. nigellastrum has the closest relationship with P. harmala.
Keywords: Zygophyllaceae, Peganum nigellastrum, chloroplast genome, phylogenetic analysis
Peganum nigellastrum Bunge belongs to Zygophyllaceae, which is a medicinal plant in the kingdom planta used in folk medicines due to insecticidal activity (Rharrabe et al. 2007), inhibition of reproduction (Nath et al. 1993; Bibi 2017) and antimicrobial activity. The decoction of dried leaves and flowers are widely used to treat gastrointestinal, hypertension, cardiac, nervous system disorders and diabetes (Moloudizargari et al. 2013). However, the chloroplast (cp) genome of P. nigellastrum has not been reported. In this study, we assembled the complete chloroplast genome of P. nigellastrum, hoping to lay a foundation for further research.
Fresh leaves of P. nigellastrum were collected from Alxa Youqi (Alxa, Inner Mongolia, China; coordinates: 101.6757E, 39.2396 N) and dried with silica gel. The voucher specimen was stored in Sichuan University Herbarium with the number of QTPLJQCHNO0293002. Total genomic DNA was extracted with a modified CTAB method (Doyle and Doyle 1987) and a library with an average insert size of 350 bp was constructed. This library was sequenced on the Illumina NovaSeq 6000 system with 150 bp paired-end reads. We obtained 10 million high quality pair-end reads for P. nigellastrum, and after removing the adapters, the remaining reads were used to assemble the complete chloroplast genome by GetOrganelle pipeline v1.6.3a (Jin et al. 2020). The complete chloroplasts genome sequence of P. harmala was used as a reference. Plann v1.1 (Huang and Cronk 2015) and Geneious v11.0.3 (Kearse et al. 2012) were used to annotate the chloroplasts genome and correct the annotation.
The total plastome length of P. nigellastrum (MW970110) is 160,066 bp, with a typical quadripartite structural organization, consisting of a large single copy (LSC) region of 88,275 bp, two inverted repeat (IR) regions of 26,486 bp and a small single copy (SSC) region of 18,855 bp. The cp genome contains 132 complete genes, including 87 protein-coding genes (87 PCGs), 8 ribosomal RNA genes (8 rRNAs), and 37 tRNA genes (37 tRNAs). Most genes occur in a single copy, while 19 genes occur in double, including 4 rRNAs (4.5S, 5S, 16S, and 23S rRNA), 7 tRNAs (trnA-UGC, trnE-UUC, trnL-CAA, trnM-CAU, trnN-GUU, trnR-ACG, and trnV-GAC), and 8 PCGs (rps7, rps19, ndhB, ycf2, ycf15, rpl2, rpl23 and rpl32). The overall GC content of cp DNA is 37.5%, the corresponding values of the LSC, SSC, and IR regions are 35.6%, 31.4%, and 42.8%.
In order to further clarify the phylogenetic position of P. nigellastrum, plastomes of 6 representative Zygophyllaceae species were obtained from NCBI to reconstruct the plastome phylogeny, with Erodium absinthoides as an outgroup. All the sequences were aligned by using MAFFT v.7.313 (Katoh and Standley 2013) and maximum likelihood phylogenetic analyses were conducted by using RAxML v.8.2.11 (Stamatakis 2014) under GTRCAT model with 500 bootstrap replicates. The phylogenetic tree shows that most the species of Zygophyllaceae were divided into two subclades (Figure 1). All Nitraria species clustered together, and all Peganum species clustered in another clade. while P. nigellastrum has the closest relationship with P. harmala.
Figure 1.
Maximum-likelihood phylogenetic tree for Peganum nigellastrum based on 7 species complete chloroplast genomes in family Zygophyllaceae.
Funding Statement
This study was funded by the doctoral scientific research foundation of the North Minzu University [2021KYQD10] and the high-level talent selection and training plan of North Minzu University [2019BJLZ02].
Disclosure statement
No potential conflict of interest was reported by the author(s).
Data availability statement
The data that support the findings of this study are openly available in GenBank of NCBI at https://www.ncbi.nlm.nih.gov, reference number MW970110. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA672277, SRA: SRS8756899, and SAMN18837312, respectively.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are openly available in GenBank of NCBI at https://www.ncbi.nlm.nih.gov, reference number MW970110. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA672277, SRA: SRS8756899, and SAMN18837312, respectively.

