Abstract
Libocedrus chevalieri is a rare endemic conifer from New Caledonia, and it is evaluated as Critically Endangered in the IUCN Red List of Threatened Species. To take conservation actions more effectively, a survey of its genomic background and evolutionary status is of great significance. Illumina paired-end reads were used to character the chloroplast (cp) genome of L. chevalieri. The circular genome is 122,068 bp in length, containing 115 genes, in which include 83 protein-coding genes, four ribosomal RNA genes, and 28 transfer RNA genes. Nine genes (atpF, rpoC1, ndhB, ndhA, rpl2, petB, rpl16, petD, rps12) have one intron, whilst one gene (ycf3) has two introns. Inverted repeat (IR) sequence doesn’t exist in the genome. The GC content of the cp genome is 34.1%. The phylogenetic analysis demonstrates that L. chevalieri has a close relationship with L. plumosa.
Libocedrus chevalieri is a rare conifer in Cupressaceae, and has been classified as Critically Endangered in the IUCN Red List of Threatened Species (Thomas Citation2010). The species is a shrub or small tree to 5 m tall and grows in high-altitude maquis shrubland at altitudes of 1,450 to 1,600 m (Farjon Citation2010; Eckenwalder Citation2009; Thomas et al. Citation2018). L. chevalieri only occur in New Caledonia on Grande Terre where is regarded as one of the world’s 25 biodiversity hotspots (Myers et al. Citation2000). However, none is known about the species’ genomic background. In this study, we used Illumina paired-end sequencing data to assemble the complete cp genome of L. chevalieri, and surveyed its phylogenetic status.
Dried leaf sample were obtained from the Royal Botanic Garden Edinburgh Herbarium (http://data.rbge.org.uk/herb/E00215054, Markus Ruhsam, [email protected], voucher number: E00215054), which were collected from New Caledonia (Latitude: 21°52′49″S, Longitude: 166°25′21″E). The whole-genome re-sequencing was conducted on the Illumina Hiseq Platform (Illumina, San Diego, CA, USA), which was deputed to BGI (https://www.genomics.cn/). After removing the adapters and low-quality reads, 3902 Mb high-quality clean reads were yielded.
GetOrganelle (Jin et al. Citation2020) was used to assemble the cp genome of L. chevalieri with the published cp genome of L. plumosa (Sudianto et al. Citation2020) as a reference, and PGA (Qu et al. Citation2019) was used to annotate the circular genome with the default parameters. Geneious Prime 2021.1.1 (https://www.geneious.com) was used to visualize the cp gene and correct the annotation result. The complete cp genome sequence was uploaded in GenBank under accession number MZ169380.
The whole cp genome of L. chevalieri is 122,068 bp in length, containing 115 genes, in which include 83 protein-coding genes, four ribosomal RNA genes, and 28 transfer RNA genes. Nine genes (atpF, rpoC1, ndhB, ndhA, rpl2, petB, rpl16, petD, rps12) have one intron, whilst one gene (ycf3) has two introns. Inverted repeat (IR) sequence doesn’t exist in the genome. The GC content of the cp genome is 34.1%.
To reveal the phylogenetic status of L. chevalieri in Cupressaceae, we downloaded nine cp genome data of species belonging to Cupressaceae from National Center for Biotechnology Information (NCBI, https://www.ncbi.nlm.nih.gov/). The sequences were aligned by MAFFT ver. 7 (https://mafft.cbrc.jp/alignment/server/index.html), and a maximum likelihood (ML) tree was reconstructed via MEGAX (Kumar et al. Citation2018) with 1000 bootstrap replicates. The ML tree () suggest that L. chevalieri is sister to L. plumosa and this relationship received a bootstrap support as high as 99.
In conclusion, the complete cp genome of this Critically Endangered species, L. chevalieri, not only provides genomic background support for its future conservation actions, but also contributes to the further phylogenetic and evolutionary studies of Libocedrus, Cupressaceae and conifers.
Acknowledgment
We thank Royal Botanic Garden Edinburgh for providing dried leaf sample of L. chevalieri.
Disclosure statement
No potential conflict of interest was reported by the author(s).
Data availability statement
The genome sequence data that support the findings of this study are openly available in GenBank of NCBI (https://www.ncbi.nlm.nih.gov/) under the accession number MZ169380. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA741855, SRX11271992 and SAMN19910176, respectively.
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References
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