Abstract
Sorbaria kirilowii is a deciduous perennial admired for its showy white blossoms. Though of importance for horticultural purposes, the plastomic study concerning this species is still lacking. Here, the plastome of S. kirilowii was de novo assembled using the high-throughput sequencing data. The complete plastome assembly of S. kirilowii was 160,810 bp in length, with a GC content of 36.03%. It featured a typical quadripartite structure, containing a pair of inverted repeats (IRs; 26,338 bp) separated by a large single-copy (LSC; 88,762 bp) and a small single-copy (SSC, 19,372 bp). In total, 132 genes were annotated in the plastome, including 87 protein-coding genes, 8 rRNA genes, and 37 tRNA genes. Furthermore, 63 SSRs, most of which were AT-rich, were identified in the cp genome of S. kirilowii. 71.7% of the cpSSRs were shown to be located in the intergenic regions. In addition, 49 repeats of varying sizes and types were also identified in the plastome. Through comparison, eight divergence hotspots were identified between the plastome of S. kirilowii and S. sorbifolia var. stellipila. These variable regions could potentially be developed into molecular markers for species delimitation or phylogenetics in future studies. We re-investigated the relationship among 17 Rosaceae species using the plastomic sequences, and S. kirilowii was shown to be a sister to S. sorbifolia var. stellipila. Overall, this study provides plastomic resources which could facilitate marker development and phylogenomics of Rosaceae.
Similar content being viewed by others
Data availability
The raw data that support the findings of this research have been deposited in the CNSA (https://db.cngb.org/cnsa/) of CNGBdb under the accession number of CNP0001053.
References
Ling-ti L (1996) The evolution and distribution of subfam. Spiraeoideae (Rosaceae) of China, with special reference to distribution of the subfamily in the world. J Syst Evol 34(4):361–375
Qu G-W, Wu C-J, Gong S-Z, Xie Z-P, Lv C-J (2016) Leucine-derived cyanoglucosides from the aerial parts of Sorbaria sorbifolia (L.) A. Braun Fitoterapia 111:102–108. https://doi.org/10.1016/j.fitote.2016.03.015
Jang J, Lee JS, Jang Y-J, Choung ES, Li WY, Lee SW, Kim E, Kim J-H, Cho JY (2020) Sorbaria kirilowii ethanol extract exerts anti-inflammatory effects in vitro and in vivo by targeting Src/nuclear factor (NF)-κB. Biomolecules 10(5):741
Jensen P, Leister D (2014) Chloroplast evolution, structure and functions. F1000prime Rep 6:40. https://doi.org/10.12703/P6-40
Roston RL, Jouhet J, Yu F, Gao H (2018) Editorial: structure and function of chloroplasts. Front Plant Sci 9:1656–1656. https://doi.org/10.3389/fpls.2018.01656
Palmer J (1990) Plastid chromosomes: structure and evolution. In: Constabel F (ed) Cell culture and somatic cell genetics of plants Vol 7A, the molecular biology of plastids. Elsevier, Amsterdam
Dobrogojski J, Adamiec M, Luciński R (2020) The chloroplast genome: a review. Acta Physiologiae Plant 42(6):98. https://doi.org/10.1007/s11738-020-03089-x
Daniell H, Lin C-S, Yu M, Chang W-J (2016) Chloroplast genomes: diversity, evolution, and applications in genetic engineering. Genome Biol 17(1):134. https://doi.org/10.1186/s13059-016-1004-2
Raubeson L, Jansen R (2005) Chloroplast genomes of plants, plant diversity and evolution: genotypic and phenotypic variation in higher plants. Divers Evol Plants. https://doi.org/10.1079/9780851999043.0045
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–e129. https://doi.org/10.1093/nar/gkt371
Dierckxsens N, Mardulyn P, Smits G (2016) NOVOPlasty: de novo assembly of organelle genomes from whole genome data. Nucleic Acids Res 45(4):e18–e18. https://doi.org/10.1093/nar/gkw955
Walker BJ, Abeel T, Shea T, Priest M, Abouelliel A, Sakthikumar S, Cuomo CA, Zeng Q, Wortman J, Young SK, Earl AM (2014) Pilon: an integrated tool for comprehensive microbial variant detection and genome assembly improvement. PLoS ONE 9(11):e112963. https://doi.org/10.1371/journal.pone.0112963
Shi L, Chen H, Jiang M, Wang L, Wu X, Huang L, Liu C (2019) CPGAVAS2, an integrated plastome sequence annotator and analyzer. Nucleic Acids Res 47(W1):W65–W73. https://doi.org/10.1093/nar/gkz345
Tillich M, Lehwark P, Pellizzer T, Ulbricht-Jones E, Fischer A, Bock R, Greiner S (2017) GeSeq - Versatile and accurate annotation of organelle genomes. Nucleic Acids Res. https://doi.org/10.1093/nar/gkx391
Greiner S, Lehwark P, Bock R (2019) OrganellarGenomeDRAW (OGDRAW) version 1.3.1: expanded toolkit for the graphical visualization of organellar genomes. Nucleic Acids Res 47:W59–W64. https://doi.org/10.1093/nar/gkz238
Mayor C, Brudno M, Schwartz JR, Poliakov A, Rubin EM, Frazer KA, Pachter LS, Dubchak I (2000) VISTA : visualizing global DNA sequence alignments of arbitrary length. Bioinformatics 16(11):1046–1047. https://doi.org/10.1093/bioinformatics/16.11.1046
Katoh K, Standley DM (2013) MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol 30(4):772–780. https://doi.org/10.1093/molbev/mst010
Rozas J, Ferrer-Mata A, Sanchez-DelBarrio JC, Guirao-Rico S, Librado P, Ramos-Onsins SE, Sanchez-Gracia A (2017) DnaSP 6: DNA sequence polymorphism analysis of large data sets. Mol Biol Evol 34(12):3299–3302. https://doi.org/10.1093/molbev/msx248
Xia X (2018) DAMBE7: new and improved tools for data analysis in molecular biology and evolution. Mol Biol Evol 35(6):1550–1552. https://doi.org/10.1093/molbev/msy073
Kurtz S, Choudhuri JV, Ohlebusch E, Schleiermacher C, Stoye J, Giegerich R (2001) REPuter: the manifold applications of repeat analysis on a genomic scale. Nucleic Acids Res 29(22):4633–4642. https://doi.org/10.1093/nar/29.22.4633
Wellington Santos M (2009) WebSat–a web software for microsatellite marker development. Bioinformation 6(3):282
Kumar S, Stecher G, Li M, Knyaz C, Tamura K (2018) MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 35(6):1547–1549. https://doi.org/10.1093/molbev/msy096
Degtjareva GV, Logacheva MD, Samigullin TH, Terentieva EI, Valiejo-Roman CM (2012) Organization of chloroplast psbA-trnH intergenic spacer in dicotyledonous angiosperms of the family Umbelliferae. Biochem Biokhimiia 77(9):1056–1064. https://doi.org/10.1134/s0006297912090131
Schroeder H, Hoeltken AM, Fladung M (2012) Differentiation of populus species using chloroplast single nucleotide polymorphism (SNP) markers–essential for comprehensible and reliable poplar breeding. Plant Biol 14(2):374
Panchy N, Lehti-Shiu M, Shiu S-H (2016) Evolution of gene duplication in plants. Plant Physiol 171(4):2294. https://doi.org/10.1104/pp.16.00523
He X, Zhang J (2005) Gene complexity and gene duplicability. Curr Biol 15(11):1016–1021. https://doi.org/10.1016/j.cub.2005.04.035
Xiong AS, Peng RH, Zhuang J, Gao F, Zhu B, Fu XY, Xue Y, Jin XF, Tian YS, Zhao W, Yao QH (2009) Gene duplication, transfer, and evolution in the chloroplast genome. Biotechnol Adv 27(4):340–347. https://doi.org/10.1016/j.biotechadv.2009.01.012
Cosner ME, Jansen RK, Palmer JD, Downie SR (1997) The highly rearranged chloroplast genome of Trachelium caeruleum (Campanulaceae): multiple inversions, inverted repeat expansion and contraction, transposition, insertions/deletions, and several repeat families. Curr Genet 31(5):419–429. https://doi.org/10.1007/s002940050225
Chang CC, Lin HC, Lin IP, Chow TY, Chen HH, Chen WH, Cheng CH, Lin CY, Liu SM, Chang CC, Chaw SM (2006) The chloroplast genome of Phalaenopsis aphrodite (Orchidaceae): comparative analysis of evolutionary rate with that of grasses and its phylogenetic implications. Mol Biol Evol 23(2):279–291. https://doi.org/10.1093/molbev/msj029
Huang J, Yang X, Zhang C, Yin X, Liu S, Li X (2015) Development of chloroplast microsatellite markers and analysis of chloroplast diversity in Chinese Jujube (Ziziphus jujuba Mill.) and Wild Jujube (Ziziphus acidojujuba Mill.). PLoS ONE 10(9):e0134519–e0134519. https://doi.org/10.1371/journal.pone.0134519
Garaycochea S, Speranza P, Alvarez-Valin F (2015) A strategy to recover a high-quality, complete plastid sequence from low-coverage whole-genome sequencing. Appl Plant Sci. https://doi.org/10.3732/apps.1500022
Li B, Huang P, Guo W, Zheng Y (2020) Development of nuclear SSR and chloroplast genome markers in diverse Liriodendron chinense germplasm based on low-coverage whole genome sequencing. Biol Res. https://doi.org/10.1186/s40659-020-00289-0
Zhang Y, Du L, Liu A, Chen J, Wu L, Hu W, Zhang W, Kim K, Lee SC, Yang TJ, Wang Y (2016) The complete chloroplast genome sequences of five epimedium species: lights into phylogenetic and taxonomic analyses. Front Plant Sci 7:306. https://doi.org/10.3389/fpls.2016.00306
Potter D, Eriksson T, Evans R, Oh S-H, Smedmark J, Morgan D, Kerr M, Robertson K, Mp A, Dickinson T, Campbell C (2007) Phylogeny and classification of Rosaceae. Plant Syst Evol 266:5–43. https://doi.org/10.1007/s00606-007-0539-9
Yu S-X, Gadagkar SR, Potter D, Xu D-X, Zhang M, Li Z-Y (2018) Phylogeny of Spiraea (Rosaceae) based on plastid and nuclear molecular data: Implications for morphological character evolution and systematics. Perspect Plant Ecol Evol Syst 34:109–119. https://doi.org/10.1016/j.ppees.2018.08.003
Potter D, Eriksson T, Evans RC, Oh S, Smedmark JEE, Morgan DR, Kerr M, Robertson KR, Arsenault M, Dickinson TA, Campbell CS (2007) Phylogeny and classification of Rosaceae. Plant Syst Evol 266(1):5–43. https://doi.org/10.1007/s00606-007-0539-9
Song J-H, Hong S-P (2020) Fruit and seed micromorphology and its systematic significance in tribe Sorbarieae (Rosaceae). Plant Syst Evol 306(1):6. https://doi.org/10.1007/s00606-020-01640-4
Funding
This research was supported by Science and Technology Project of Qinghai Province (2019-ZJ-962Q; 2019-NK-106; 2018-ZJ-963Q; 2017-NK-151; 2016-ZJ-Y01), The Open Project of State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University (2019-ZZ-05), and The Youth Foundation of Qinghai University (2019-QNY-2).
Author information
Authors and Affiliations
Contributions
LW designed and supervised the project, reviewed drafts of the paper; LW and JL conceived the conception, analyzed the data and wrote the original draft manuscript; LW and QS. analyzed the data and checked and revised the manuscript; JL and WS participated in analyzing the data and drew some figures and tables; LW collected the samples and provided some advice.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval
This article does not contain any studies with human participants performed by any of the authors.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Wang, L., Liang, J., Shang, Q. et al. The complete plastome of Sorbaria kirilowii: genome structure, comparative analysis, and phylogenetic implications. Mol Biol Rep 47, 9677–9687 (2020). https://doi.org/10.1007/s11033-020-05976-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11033-020-05976-5