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Mitochondrial DNA. Part B, Resources logoLink to Mitochondrial DNA. Part B, Resources
. 2020 Feb 11;5(1):1096–1097. doi: 10.1080/23802359.2020.1721368

Characterization of the complete chloroplast genome of the Pohlia nutans M211 from Antarctica

Qing Jin a,b,*, Liping Zhang a,*, Dan Li a, Yingying He b, Changfeng Qu b,c,, Jinlai Miao a,b,c,
PMCID: PMC7748587  PMID: 33366890

Abstract

The Antarctic Pohlia nutans M211 complete chloroplast (cp) genome, sequenced using Illumina NovaSeq PE150, was 125,199 bp in length. It contained 19,836 bp of inverted repeat (IR) regions that separated a large single-copy region (LSC) of 86,738 bp and a small single-copy region (SSC) of 18,580 bp. The whole-genome encodes 132 genes (80 protein-coding genes, 36 tRNA genes, and 8 rRNA genes) and had 29.5% GC content. The M211 was congruent with Sanionia uncinata (KM111545.1) according to the Phylogenetic tree analyses.

Keywords: Pohlia nutans M211, chloroplast genome, phylogenetic tree


Antarctica terrestrial ecosystem is cold, limited water, and low nutrient environment, accompanied by sharp temperature changes (Campbell and Claridge 1988; Pearce 2008; Singh et al. 2011). Mosses are the most widespread and abundant photo-synthetically active plant along with and near the islands of the Antarctic continent (Wahrmund et al. 2010). Although moss is a lower group of higher plants in terms of phylogeny (Malenovky et al. 2013), it represents a type of plant that has transitioned from aquatic to terrestrial. The moss is one of the ideal materials to study plant resistance because of the cold, strong radiation of the special living environment, which expected to obtain a number of functional genes with important application value (Moss 2006). Here, we completed the chloroplast genome of Pohlia nutans M211 that isolated from the Antarctic land during the 24th Antarctic expedition.

Pohlia nutans M211 was preserved in the Key Laboratory of Marine Bioactive Substances, the First Institute of Oceanography, Ministry of Natural Resource, China. The Genomic DNA of M11 was extracted with the SDS method (Lim et al. 2016) and sequenced using Illumina NovaSeq PE150 at the Beijing Novogene Bioinformatics Technology Co., Ltd., moreover, it was assembled with SOAP DeNovo software and predicted with GeneMarkS.

The complete chloroplast (cp) genome of P. nutans M211 (GenBank accession MN937553) was 125,199 bp in length and GC ratio was 29.2%. Additionally, it had a large single-copy (LSC) region of 86,738 bp, a small single-copy (SSC) region of 18,580 bp, a pair inverted repeat (IR) regions of 19,836 bp each, and contained 124 genes: 80 protein-coding genes, 8 rRNAs, and 36 tRNAs.

We conducted a phylogenetic analysis to identify the phylogenetic position of P. nutans M211, and was based on 14 selected Bryophytina chloroplast genome sequences and two species [Encephalartos lehmannii (LC049336.1), Cathaya argyrophylla (AB547400.1)] as the outgroup to reconstruct by neighbor-joining (NJ) phylogenetic tree in MEGA. The bootstrap value was 1000. The phylogenetic evidence revealed that the P. nutans M211 was closely related to Sanionia uncinata (KM111545.1) (Figure 1). The result of our study lays the foundation to obtain the functional genes with important application value from mosses.

Figure 1.

Figure 1.

Neighbor-joining (bootstrap repeat was 1000) phylogenetic tree of 16 complete chloroplast genomes.

Funding Statement

This work was supported by National Key Research and Development Program of China [2018YFD0900705], the China Ocean Mineral Resources Research and Development Association [DY135-B2-14], and Natural Science Foundation of Shandong Province [ZR2019BD023].

Disclosure statement

No potential conflict of interest was reported by the authors.

References

  1. Campbell IB, Claridge GGC. 1988. Landscape evolution in Antarctica. Earth Sci Rev. 25(5–6):345–353. [Google Scholar]
  2. Lim HJ, Lee E-H, Yoon Y, Chua B, Son A. 2016. Portable lysis apparatus for rapid single‐step DNA extraction of Bacillus subtilis. J Appl Microbiol. 120(2):379–387. [DOI] [PubMed] [Google Scholar]
  3. Malenovky Z, Lucieer A, Robinson S, Harwin S, Turner D, Veness T. 2013. Monitoring of Antarctic moss ecosystems using a high spatial resolution imaging spectroscopy. Vienna (Austria): EGU General Assembly. [Google Scholar]
  4. Moss L. 2006. Redundancy, plasticity, and detachment: the implications of comparative genomics for evolutionary thinking. Phil Sci. 73(5):930–946. [Google Scholar]
  5. Pearce DA. 2008. Climate change and the microbiology of the Antarctic Peninsula region. Sci Prog. 91(2):203–217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Singh J, Dubey AK, Singh RP. 2011. Antarctic terrestrial ecosystem and role of pigments in enhanced UV-B radiations. Rev Env Sci Biotechnol. 10(1):63–77. [Google Scholar]
  7. Wahrmund U, Quandt D, Knoop V. 2010. The phylogeny of mosses - addressing open issues with a new mitochondrial locus: Group i intron cobi420. Mol Phylogenet Evol. 54(2):417–426. [DOI] [PubMed] [Google Scholar]

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