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Therapeutic Methods and Therapies TCIM
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1.
Int J Mol Sci ; 20(9)2019 May 04.
Article in English | MEDLINE | ID: mdl-31060231

ABSTRACT

Three Apiaceae species Ledebouriella seseloides, Peucedanum japonicum, and Glehnia littoralis are used as Asian herbal medicines, with the confusingly similar common name "Bang-poong". We characterized the complete chloroplast (cp) genomes and 45S nuclear ribosomal DNA (45S nrDNA) sequences of two accessions for each species. The complete cp genomes of G. littoralis, L. seseloides, and P. japonicum were 147,467, 147,830, and 164,633 bp, respectively. Compared to the other species, the P. japonicum cp genome had a huge inverted repeat expansion and a segmental inversion. The 45S nrDNA cistron sequences of the three species were almost identical in size and structure. Despite the structural variation in the P. japonicum cp genome, phylogenetic analysis revealed that G. littoralis diverged 5-6 million years ago (Mya), while P. japonicum diverged from L. seseloides only 2-3 Mya. Abundant copy number variations including tandem repeats, insertion/deletions, and single nucleotide polymorphisms, were found at the interspecies level. Intraspecies-level polymorphism was also found for L. seseloides and G. littoralis. We developed nine PCR barcode markers to authenticate all three species. This study characterizes the genomic differences between L. seseloides, P. japonicum, and G. littoralis; provides a method of species identification; and sheds light on the evolutionary history of these three species.


Subject(s)
Apiaceae/classification , Apiaceae/genetics , DNA Barcoding, Taxonomic , Gene Rearrangement , Genome, Chloroplast , Plants, Medicinal/classification , Plants, Medicinal/genetics , Chloroplasts/genetics , DNA Copy Number Variations , Genomics/methods , Mutation , Open Reading Frames , Phylogeny , RNA, Ribosomal/genetics , Sequence Analysis, DNA , Tandem Repeat Sequences
2.
Mol Phylogenet Evol ; 126: 181-195, 2018 09.
Article in English | MEDLINE | ID: mdl-29684597

ABSTRACT

Mikania micrantha and Mikania cordata are the only two species in genus Mikania (Asteraceae) in China. They share very similar morphological and life-history characteristics but occupy quite different habitats. Most importantly, they generate totally different ecological consequences. While M. micrantha has become an exotic invasive weed, M. cordata exists as an indigenous species with no harmful effects on native plants or habitats. As a continuous study of our previously reported M. micrantha chloroplast (cp) genome, in this study we have further sequenced the M. cordata cp genome to (1) conduct a comparative genome analysis to gain insights into the mechanism of invasiveness; (2) develop cp markers to examine the population genetic adaptation of M. micrantha; and (3) screen variable genome regions of phylogenetic utility. The M. cordata chloroplast genome is 151,984 bp in length and displays a typical quadripartite structure. The number and distribution of protein coding genes, tRNA genes, and rRNA genes of M. cordata are identical to those of M. micrantha. The main difference lays in that the pseudogenization of ndhF and a 118-bp palindromic repeat only arises in M. cordata. Fourteen highly divergent regions, 235 base substitutions, and 58 indels were identified between the two cp genomes. Phylogenetic inferences revealed a sister relationship between M. micrantha and M. cordata whose divergence was estimated to occur around 1.78 million years ago (MYA). Twelve cpSSR loci were detected to be polymorphic and adopted to survey the genetic adaptation of M. micrantha populations. No cpSSR loci were found to undergo selection. Our results build a foundation to examine the invasive mechanism of Mikania weed.


Subject(s)
Genome, Chloroplast , Genomics , Introduced Species , Mikania/classification , Mikania/genetics , Phylogeny , Plant Weeds/classification , Plant Weeds/genetics , Asteraceae/genetics , China , Chloroplasts , Chromosome Mapping , Microsatellite Repeats/genetics , Mutation/genetics , Open Reading Frames/genetics , Sequence Analysis, DNA , Time Factors
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