The complete chloroplast genome of Acer fabri (Aceraceae)

DOI: https://doi.org/10.21203/rs.3.rs-1947175/v1

Abstract

Acer fabri is endemic to the provinces of Guangdong, Jiangxi, Hunan, and Sichuan in China. This study sequenced and analyzed the complete chloroplast (cp) genome of A. fabri. The cp genome was 156,918 bp in length, including a large single-copy (LSC) region of 85,309 bp, a small single-copy (SSC) region of 18,103 bp, and a pair of invert repeats (IR) regions of 26,753 bp. The analyses predicted 113 genes, including 79 protein-coding genes, 31 tRNA genes, and 4 rRNA genes. The overall GC content of the complete cp genome was 37.90%. Phylogenetic analysis further suggested that A. fabri was closely related to A. olivaceum, with high bootstrap values.

Full Text

Acer fabri is a small evergreen tree of the family Aceraceae Juss (Acer fabri Hance, 1884; Chen B-H. et al. 2019), having bright red leaves and dense branches (Li Q-Z et al. 2008Chen B-H. et al. 2019). Native to the provinces of Guangdong, Jiangxi, Hunan, and Sichuan in China, the species is suitable for use as a second layer of canopy configuration and for landscape forests, ecological forests, and as a greening tree species (Ji Hua et al. 2012). This study reports the complete chloroplast (cp) genome sequence of A. fabri to serve as a reference for future genetic studies.

The research method for this study was approved by the Guizhou Forestry Bureau (http://www.gzslky.com/). Fresh leaf samples of A. fabri were collected from the Guizhou Academy of Forestry, Guiyang City, Guizhou Province, China (106°14′14″E, 26°29′57″N). The specimen (voucher number 09013526) was deposited at the Guizhou Academy of Forestry (http://www.gzslky.com/, Chen Zhi-ping and [email protected]).High-throughput sequencing was carried out using the Illumina Novaseq 6000 with 150bp pair-end reads. In all, 1Gb raw clean reads were generated.The chloroplast genome was assembled using MITObim v1.9 (Hahn et al. 2013). The annotated genome was deposited in the NCBI GenBank under the accession number MZ664553 (Ku et al. 2013). The phylogenetic tree was further constructed using the IQ-TREE software (Kalyaanamoorthy et al. 2017; Hoang et al. 2018). 

The cp genome sequence of A. fabri was revealed to be 156,918 bp in length, with a large single-copy (LSC) region of 85,309 bp, a small single-copy (SSC) region of 18,103 bp, and a pair of invert repeats (IR) regions of 26,753 bp. A total of 113 genes were predicted, including 78 protein-coding genes, 31 tRNA genes, and 4 rRNA genes, having an overall GC content of 37.90%. 

To further examine the phylogenetic position of A. fabri, the complete cp genome sequences of the 72 representative species of Acer were downloaded from the NCBI GenBank database for phylogenetic analysis.The complete cp genome sequences were aligned using MAFFT v7.307 (Katoh et al. 2013) and MEGA ver. 7 (Kumar et al. 2016). The resultant ML tree indicated that A. fabri and A. olivaceum (MW067059) formed a strongly supported clade, belonging to Aceraceae. The sister genus Dipteronia with its two species Dipteronia dyeriana (KT985457) and Dipteronia sinensis (KT878501) are considered as out group.

Declarations

Disclosure statement 

No potential conflict of interest was reported by the authors. 

Funding

This study was supported by the forestry scientific research project of Guizhou Forestry Bureau,  Study on the control technology of Beauveria bassiana on Alcidodes juglans Chao(Qian Lin Ke He J[2020]8).

Data availability statement

The genome sequence data that support the findings of this study are openly available in GenBank of NCBI at [https://www.ncbi.nlm.nih.gov] under the accession NO.MZ664553. The associated BioProject, SRA, and Bio-Sample numbers are PRJNA769527, SRX12524699 and SAMN22139691 respectively.

Author contributions

Yu-xue Zhao and Xia Yang designed and executed the experiment, completed the data analysis, and wrote the first draft of the paper. Jia-Min Zhu and Liu-Yan Wu participated in the experimental design and analysis of the results. All the authors have read and agreed to the final version of the manuscript. 

References

  1. Chen BH, Jiang B, Deng YS, Zhang J, Hu MF (2019) The seedling and cutting propagation techniques of Acer fabri Hance. Vegetos 32(1):98–102
  2. Hahn C, Bachmann L, Chevreux B (2013) Reconstructing mitochondrial genomes directly from genomic next-generation sequencing reads–a baiting and iterative mapping approach. Nucleic Acids Res 41(13):e129
  3. Hoang DT, Chernomor O, von Haeseler A, Minh BQ, Vinh LS (2018) UFBoot2: improving the ultrafast bootstrap approximation. Mol Biol Evol 35(2):518–522
  4. Ji H, Fu Q, Jiang DW, Shao L, Cheng LQ (2012) Physiological and Morphological Changes of Acer fabri Seedlings under Drought Stress. Acta Agriculturae Jiangxi 24(1):1–4
  5. Kalyaanamoorthy S, Minh BQ, Wong TKF, von Haeseler A, Jermiin LS (2017) ModelFinder: fast model selection for accurate phylogenetic estimates. Nat Methods 14(6):587–589
  6. Katoh K, Standley DM (2013) MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol 30:772–780
  7. Ku C, Hu JM, Kuo CH (2013) Complete Plastid Genome Sequence of the Basal Asterid Ardisia polysticta Miq. and Comparative Analyses of Asterid Plastid Genomes. PLoS ONE 8(4):e62548
  8. Kumar S, Stecher G, Tamura K (2016) MEGA7: Molecular Evolutionary Genetics Analysis Version 7.0 for Bigger Datasets. Mol Biol Evol 33:1870–1874
  9. Li QZ, Liu XH, Su JL (2008) Research progress of Aceraceae in China. Jiangsu agricultural sciences 6:184–186