Abstract
The Socotra dragon`s blood tree (Dracaena cinnabari Balf.) is endemic to the island of Socotra in Yemen. This iconic species plays an essential role in the survival of associated organisms, acting as an umbrella tree. Overexploitation, overgrazing by livestock, global climate change, and insufficient regeneration mean that the populations of this valuable species are declining in the wild. Although there are many studies on the morphology, anatomy, and physiology of D. cinnabari, no genomic analysis of this endangered species has been performed so far. Therefore, the main aim of this study was to characterize the complete chloroplast sequence genome of D. cinnabari for conservation purposes. The D. cinnabari chloroplast genome is 155,371 bp with a total GC content of 37.5%. It has a quadripartite plastid genome structure composed of one large single-copy region of 83,870 bp, one small single-copy region of 18,471 bp, and two inverted repeat regions of 26,515 bp each. One hundred and thirty-two genes were annotated, 86 of which are protein-coding genes, 38 are transfer RNAs, and eight are ribosomal RNAs. Forty simple sequence repeats have also been identified in this chloroplast genome. Comparative analysis of complete sequences of D. cinnabari chloroplast genomes with other species of the genus Dracaena showed a very high conservativeness of their structure and organization. Phylogenetic inference showed that D. cinnabari is much closer to D. draco, D. cochinchinensis, and D. cambodiana than to D. terniflora, D. angustifolia, D. hokouensis, and D. elliptica. The results obtained in this study provide new and valuable omics data for further phylogenetic studies of the genus Dracaena as well as enable the protection of genetic resources of highly endangered D. cinnabari.
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