Mechanisms underlying flower color variation in Asian species ofMeconopsis: A preliminary phylogenetic analysis based on chloroplast DNA and anthocyanin biosynthesis genes
Abstract:The Qinghai-Tibet Plateau (QTP) harbors the highest species diversity of alpine plants in the world, with a spectacular diversity of flower colors. Among these QTP plants, the genus Meconopsis comprises more than 50 species, for which flower color is a key diagnostic character. However, the mechanisms underlying flower color variation have rarely been investigated. In the present study, we used three chloroplast (cp) DNA fragments and two anthocyanin biosynthesis genes (F3H and F3 0 H) for phylogenetic reconst… Show more
“…Although flower colour is changeable in Meconopsis, these two types of colour are usually incompatible and have different pigment bases. Red, violet or blue are due to different derivatives from the anthocyanin biosynthetic pathway, while yellow is due to suppression of anthocyanin (Zhao et al 2014) or dominated by some different compound (Acheson et al 1962, Ono et al 2006. In the natural environment, it is easy to find colour mutations in blue Meconopsis, such as M. horridula and M. grandis, however, the flower colour in yellow Meconopsis, such as M. integrifolia and M. sulphurea is more stable.…”
Section: Identity Of Meconopsis Castaneamentioning
The taxonomic distinction between Meconopsis georgei G. Taylor and M. castanea H. Ohba, T. Yoshida & H. Sun has been disputed in recent times. Due to its limited distribution area, M. georgei had not been recollected since its publication and given the lack of observation of living plants and specimens, M. castanea was treated as a form of M. georgei. However, After field investigations and careful examination of type specimens, we provide an expanded description of M. georgei and suggest that M. castanea should be restored as an independent species. A molecular phylogenetic analysis also supports this conclusion.
“…Although flower colour is changeable in Meconopsis, these two types of colour are usually incompatible and have different pigment bases. Red, violet or blue are due to different derivatives from the anthocyanin biosynthetic pathway, while yellow is due to suppression of anthocyanin (Zhao et al 2014) or dominated by some different compound (Acheson et al 1962, Ono et al 2006. In the natural environment, it is easy to find colour mutations in blue Meconopsis, such as M. horridula and M. grandis, however, the flower colour in yellow Meconopsis, such as M. integrifolia and M. sulphurea is more stable.…”
Section: Identity Of Meconopsis Castaneamentioning
The taxonomic distinction between Meconopsis georgei G. Taylor and M. castanea H. Ohba, T. Yoshida & H. Sun has been disputed in recent times. Due to its limited distribution area, M. georgei had not been recollected since its publication and given the lack of observation of living plants and specimens, M. castanea was treated as a form of M. georgei. However, After field investigations and careful examination of type specimens, we provide an expanded description of M. georgei and suggest that M. castanea should be restored as an independent species. A molecular phylogenetic analysis also supports this conclusion.
“…In plant species, the cp genome is widely used for phylogenetic analyses and molecular marker development to improve phylogenetic resolution at the interspecific level. A great deal of research has been conducted using molecular markers in the study of the phylogeny of the genus Meconopsis [16,17]. Previous studies have complemented previous morphology-based treatments on the phylogenetic relationships of a few Meconopsis species through large-scale sampling and the construction of phylogenetic models using molecular markers [5].…”
The Meconopsis species are widely distributed in the Qinghai-Tibet Plateau, Himalayas, and Hengduan Mountains in China, and have high medicinal and ornamental value. The high diversity of plant morphology in this genus poses significant challenges for species identification, given their propensity for highland dwelling, which makes it a question worth exploring how they cope with the harsh surroundings. In this study, we recently generated chloroplast (cp) genomes of two Meconopsis species, Meconopsis paniculata (M. paniculata) and M. pinnatifolia, and compared them with those of ten Meconopsis cp genomes to comprehend cp genomic features, their phylogenetic relationships, and what part they might play in plateau adaptation. These cp genomes shared a great deal of similarities in terms of genome size, structure, gene content, GC content, and codon usage patterns. The cp genomes were between 151,864 bp and 154,997 bp in length, and contain 133 predictive genes. Through sequence divergence analysis, we identified three highly variable regions (trnD-psbD, ccsA-ndhD, and ycf1 genes), which could be used as potential markers or DNA barcodes for phylogenetic analysis. Between 22 and 38 SSRs and some long repeat sequences were identified from 12 Meconopsis species. Our phylogenetic analysis confirmed that 12 species of Meconopsis clustered into a monophyletic clade in Papaveraceae, which corroborated their intrageneric relationships. The results indicated that M. pinnatifolia and M. paniculata are sister species in the phylogenetic tree. In addition, the atpA and ycf2 genes were positively selected in high-altitude species. The functions of these two genes might be involved in adaptation to the extreme environment in the cold and low CO2 concentration conditions at the plateau.
“…Mao, Li (7) studied eight morphometric traits of cone and seeds in Pinus densata and the parental species and concluded that Pinus densata is more reproductively successful in the natural habitat than the local Pinus tabuliformis and Pinus yunnanensis. Among the three Pinus species, the cross barrier is weak and the fitness differences are determined by local adaptation [8] . These phenotyping assessments are laborious to compare the interspecific variation, involving field sampling, common garden trials, experimental measurement and destructive evaluation methods.…”
We evaluated a novel and non-destructive method of the electrical impedance spectroscopy (EIS) to elucidatethe genetic and evolutionary relationship of homoploid hybrid conifer of Pinus densata (P.d) and its parental species Pinus tabuliformis (P.t) and Pinus yunnanensis(P.y), as well as the artificial hybrids of the P.t and P.y. Field common garden tests of96 trees sampled from 760 seedlings and 480 EIS records of 1,440 needles assessed the interspecific variation of the P.d, P.t, P.y and the artificial hybrids. We found that (1) EIS at different frequencies diverged significantly among germplasms; P.ywasthe highest, P.t was the lowest, and their artificial hybrids were within the range of P.t and P.y; (2) maternal species effect of EIS magnitudes inthe hybrids and P.d was stronger than the paternal species characteristics; (3)EIS of the artificial hybrid confirmed the mid-parent and partial maternal species characteristics;(4) unified exponential modelof EIS for the interspecific and hybrids canbe constructedas; (5) cluster analysis for species and hybrid combinationsin total corroborated with the previous hybrid model ofPinus densata. Our non-destructive EIS method complemented the previous finding that Pinus densata was originated from P.t and P.y. We conclude that the impedance would be a viable indicator to investigate the interspecific genetic variations of conifers.
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