摘要
Panax stipuleanatus(Araliaceae) is an endangered and medicinally important plant endemic to China.However, phylogenetic relationships within the genus Panax have remained unclear. In this study, we sequenced the complete plastome of P. stipuleanatus and included previously reported Panax plastomes to better understand the relationships between species and plastome evolution within the genus Panax.The plastome of P. stipuleanatus is 156,069 base pairs(bp) in length, consisting of a pair of inverted repeats(IRs, each 25,887 bp) that divide the plastome into a large single copy region(LSC, 86,126 bp) and a small single copy region(SSC, 8169 bp). The plastome contains 114 unigenes(80 protein-coding genes,30 tRNA genes, and 4 r RNA genes). Comparative analyses indicated that the plastome gene content and order, as well as the expansion/contraction of the IR regions, are all highly conserved within Panax. No significant positive selection in the plastid protein-coding genes was observed across the eight Panax species, suggesting the Panax plastomes may have undergone a strong purifying selection. Our phylogenomic analyses resulted in a phylogeny with high resolution and supports for Panax. Nine proteincoding genes and 10 non-coding regions presented high sequence divergence, which could be useful for identifying different Panax species.
Panax stipuleanatus(Araliaceae) is an endangered and medicinally important plant endemic to China.However, phylogenetic relationships within the genus Panax have remained unclear. In this study, we sequenced the complete plastome of P. stipuleanatus and included previously reported Panax plastomes to better understand the relationships between species and plastome evolution within the genus Panax.The plastome of P. stipuleanatus is 156,069 base pairs(bp) in length, consisting of a pair of inverted repeats(IRs, each 25,887 bp) that divide the plastome into a large single copy region(LSC, 86,126 bp) and a small single copy region(SSC, 8169 bp). The plastome contains 114 unigenes(80 protein-coding genes,30 tRNA genes, and 4 r RNA genes). Comparative analyses indicated that the plastome gene content and order, as well as the expansion/contraction of the IR regions, are all highly conserved within Panax. No significant positive selection in the plastid protein-coding genes was observed across the eight Panax species, suggesting the Panax plastomes may have undergone a strong purifying selection. Our phylogenomic analyses resulted in a phylogeny with high resolution and supports for Panax. Nine proteincoding genes and 10 non-coding regions presented high sequence divergence, which could be useful for identifying different Panax species.
基金
financially supported by the Major Program of National Natural Science Foundation of China (No. 31590823)
the National Natural Science Foundation of China (No. 31070297)
