ABSTRACT
OBJECTIVE@#To observe the effect of acupuncture combined with regular treatment and swallowing function training on pharyngeal motor, sensory function and penetration-aspiration function in patients with dysphagia after stroke.@*METHODS@#A total of 60 patients with dysphagia after stroke were randomly divided into a control group and an observation group, 30 patients in each group. Both groups were treated with conventional treatment and swallowing function training; in addition, the observation group was treated with acupuncture at Lianquan (CV 23), Fengfu (GV 16), Yifeng (TE 17). All the treatments were given once a day, 5 days a week, for totally 4 weeks. In the two groups, the pharyngeal motor and sensory function, penetration-aspiration scores were evaluated by fiberoptic endoscopic evaluation of swallowing (FEES), and the Kubota water swallowing test scores were assessed before and after treatment, and the clinical effects were compared.@*RESULTS@#After treatment, the pharyngeal motor and sensory function in the two groups were all higher than those before treatment (P<0.05), and those in the observation group were better than the control group (P<0.05). After treatment, the penetration-aspiration scores and Kubota water swallowing test scores in the two groups were all lower than those before treatment (P<0.05), and those in the observation group were lower than the control group (P<0.05). The total effective rate was 93.3% (28/30) in the observation group, which was better than 73.3% (22/30) in the control group (P<0.05).@*CONCLUSION@#Acupuncture combined with regular treatment and swallowing training could improve the pharyngeal motor and sensory function, and penetration-aspiration scores in patients with dysphagia after stroke.
Subject(s)
Humans , Acupuncture Points , Acupuncture Therapy , Deglutition , Deglutition Disorders/therapy , Stroke/complications , Treatment Outcome , WaterABSTRACT
Silent information regulator 1 (Sirt1) is a deacetylase, which plays an important role in the occurrence and development of diabetic nephropathy (DN). Our previous study shows that Yin yang 1 (YY1), a widely expressed zinc finger DNA/RNA-binding transcription factor, is a novel regulator of renal fibrosis in diabetic nephropathy. Since the activity of YY1 is regulated via acetylation and deacetylation modification, this study aimed to explore whether Sirt1-induced deacetylation of YY1 mediated high glucose (HG)-induced renal tubular epithelial-mesenchymal transition (EMT) and renal fibrosis in vivo and in vitro. We first confirmed that Sirt1 expression level was significantly decreased in the kidney of db/db mice and in HG-treated HK-2 cells. Diabetes-induced Sirt1 reduction enhanced the level of YY1 acetylation and renal tubular EMT. Then, we manipulated Sirt1 expression in vivo and in vitro by injecting resveratrol (50 mg·kg-1·d-1. ip) to db/db mice for 2 weeks or application of SRT1720 (2.5 µM) in HG-treated HK-2 cells, we found that activation of Sirt1 reversed the renal tubular EMT and YY1 acetylation induced by HG condition. On the contrary, Sirt1 was knocked down in db/m mice or EX527 (1 µM) was added in HK-2 cells, we found that inhibition of Sirt1 exacerbated renal fibrosis in diabetic mice and enhanced level of YY1 acetylation in HK-2 cells. Furthermore, knockdown of YY1 inhibited the ameliorating effect of resveratrol on renal tubular EMT and renal fibrosis in db/db mice. In conclusion, this study demonstrates that Sirt1 plays an important role in renal tubular EMT of DN through mediating deacetylation of YY1.
Subject(s)
Diabetes Mellitus, Experimental/complications , Diabetic Nephropathies/physiopathology , Sirtuin 1/genetics , YY1 Transcription Factor/metabolism , Animals , Cell Line , Diabetes Mellitus, Experimental/genetics , Diabetic Nephropathies/genetics , Epithelial-Mesenchymal Transition/genetics , Fibrosis , Gene Knockdown Techniques , Glucose/metabolism , Heterocyclic Compounds, 4 or More Rings/pharmacology , Humans , Male , Mice , Resveratrol/pharmacology , YY1 Transcription Factor/geneticsABSTRACT
Paecilomyces hepiali is a new species of fungus isolated from a field collection of Ophiocordyceps sinensis from Baima snow mountain, Diqing Tibetan Autonomous Prefecture, Yunnan Province by the Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences. The specimen was identified and named as Paecilomyces hepiali by Qing-Tao Chen, the professor of the Institute of Microbiology, Chinese Academy of Sciences (Paecilomyces hepiali) (2008), who identified a dried culture of living strain 82-2 as the holotype. Until now, the holotype (the voucher specimen) was deposited in the Herbarium of the Institute of Chinese Materia Medica (HICMM), China Academy of Chinese Medical Sciences, Beijing. The P. hepiali neotype designated by the paper "Neotypification of P. hepiali (Hypocreales)" published in TAXON 64 (1) by Yao Yi-Jian et al. in February 2015 is untenable.
ABSTRACT
Suspension cultures cell of Sorbus aucuparia (SASC) was used as materials, the changes of physiological and biochemical indexes of SASC after treatment with yeast extract (YE) were detected, and the synthetic mechanism of secondary metabolites in SASC treated with YE was preliminarily explored. The results were as follows: under the assay conditions, SASC was induced to synthesize five biphenyl compounds, and these compounds content changed differently with induction time prolonging; YE treatment inhibited cell growth, the culture medium pH was gradually reduced after treatment; water-soluble protein content showed a trend of slow decline, which was significantly increased in YE treatment group (YE group) compared with the control group (CK group), the maximum relative content was 147.76% in contrast with CK group; both YE group and CK group were extracellular Ca2+ flow influx, but the YE group flow was significantly slow than CK group. The results indicate that YE induced the cells in a stress state, which was not conducive to the growth of cells and forced the cells to synthesize biphenyl compounds against external stress; water-soluble protein may serve as intracellular enzymes involved in the synthesis of compounds regulation; Ca2+ may as signal molecule mediate cell signal transduction respond to YE stress.
Subject(s)
Cell Culture Techniques , Methods , Culture Media , Chemistry , Metabolism , Saccharomyces cerevisiae , Chemistry , Secondary Metabolism , Sorbus , MetabolismABSTRACT
Single nucleotide polymorphisms (SNP) is an important molecular marker in traditional Chinese medicine research, and it is widely used in TCM authentication. The present study created a new genotyping method by combining restriction endonuclease digesting with melting curve analysis, which is a stable, rapid and easy doing SNP genotyping method. The new method analyzed SNP genotyping of two chloroplast SNP which was located in or out of the endonuclease recognition site, the results showed that when attaching a 14 bp GC-clamp (cggcgggagggcgg) to 5' end of the primer and selecting suited endonuclease to digest the amplification products, the melting curve of Lonicera japonica and Atractylodes macrocephala were all of double peaks and the adulterants Shan-yin-hua and A. lancea were of single peaks. The results indicated that the method had good stability and reproducibility for identifying authentic medicines from its adulterants. It is a potential SNP genotyping method and named restriction endonuclease digest - melting curve analysis.
Subject(s)
Atractylodes , Classification , Genetics , DNA Restriction Enzymes , Metabolism , DNA, Plant , Genetics , Drug Contamination , Genotype , Lonicera , Classification , Genetics , Plants, Medicinal , Classification , Genetics , Polymorphism, Single NucleotideABSTRACT
By reverse transcription-polymerase chain reaction (RT-PCR), an open reading frame of pathogenesis-related protein 1 (PR1) was isolated from Panax notoginseng and named as PnPR1. Molecular and bioinformatic analyses of PnPR1 revealed that an open reading frame of 501 bp was predicted to encode a 166-amino acid protein with a deduced molecular mass of 18.1 kD. Homology analysis showed that the deduced amino acid sequence of PR1 protein of Panax notoginseng had a high similarity with other higher plants had the same conservative structure domain of cysteine-rich secretory protein (CAP). The recombinant expressed plasmid pET28a(+)-PnPR1 was expressed in Escherichia coli BL21. The expression conditions were optimized by induction at different times, different temperatures, different IPTG concentrations and different giving times. The optimum expression condition was 0.4 mmol.L-1 IPTG at 28 degrees C for 20 h. The successful expression of PnPR1 provides some basis for protein purification and preparation of the monoclonal antibody.
Subject(s)
Amino Acid Sequence , Cloning, Molecular , Escherichia coli , Metabolism , Molecular Weight , Open Reading Frames , Genetics , Panax notoginseng , Chemistry , Phylogeny , Plant Proteins , Genetics , Metabolism , Plants, Medicinal , Chemistry , Reverse Transcriptase Polymerase Chain Reaction , Sequence AlignmentABSTRACT
Via studying the phenotype, growth curve and secondary metabolites of two kinds of suspension culture cell of Arnebia euchroma, the kinetics parameters of growth and accumulation of shikonin compounds in cell suspension culture of A. euchroma was obtained through simulating and modeling. This Study found that the red high-yielding one was a fine cell line for producing shikonin compounds, and the white low-yielding one may be a mutant. The first-order and second-order derivative of the fitting function were obtained by fitting the Logistic model of growth curve to get the growth rate and growth acceleration curve of the suspended cells. It is found that the best period to subculture was the 15th day cultured in fresh medium, and the best period of the induction process was the 13th-14th day. When compared the growth rate of the red line and the shikonin compounds accumulation curve, it is found that the rapid growth of the biomass of cells was not conducive to the synthesis and accumulation of shikonin compounds.
Subject(s)
Boraginaceae , Chemistry , Cell Biology , Metabolism , Cell Culture Techniques , Cell Proliferation , Naphthoquinones , Metabolism , Plant CellsABSTRACT
Objective To preliminarily understand the genotyping characteristics regarding the variable number tandem repeats (VNTR) of Mycobacterium tuberculosis clinical isolates so as to provide evidence for the development of tuberculosis control and prevention programs in Fujian province.Methods Fifteen VNTR locus sets were used to detect the clinical isolates from the fifth surveillance project on tuberculosis resistance,in Fujian province.BioNumerics version 4.5 were used to analyze the cluster from the results generated by genotyping.Results 313 Mycobacterium tuberculosis isolates were divided into 9 clusters,including Ⅰ,Ⅱ,Ⅲ,Ⅳ,Ⅴ,Ⅵ,Ⅶ,Ⅷ and Ⅸ,with the number of 220,9,48,2,1,3,10,10,10 isolates,respectively.Cluster Ⅰ was the major lineage,accounting for 70.3% (220/313) of the total.Resistance rates of cluster Ⅰ isolates to isoniazid,streptomycin,ethambutol and multi-drug-resistaut were not statistically different from other clusters (P>0.05).However,resistance rate to rifampicin (RFP) was significantly higher than that of other isolates of the clusters,33.2% (73/220) vs.20.4% (19/93) (P<0.05).Conclusion The strains isolated from Fujian province showed significant polymorphism on genotyping.Cluster Ⅰ seemed to be the dominant,calling for the close monitoring program on cluster Ⅰ strains.Results from our initial studies demonstrated the existence of significant correlation between cluster Ⅰ strains and drug resistance to RFP.
ABSTRACT
<p><b>OBJECTIVE</b>To investigate potential mutation of PHOX2A (or ARIX) gene in a Chinese family affected with congenital fibrosis of extraocular muscles tyep 2 (CFEOM2).</p><p><b>METHODS</b>Genomic DNA was obtained from affected and unaffected members of the family. With an ABI PRSIM Linkage Mapping Set-MD10 kit, selected markers flanking the PHOX2A locus were used for linkage analysis. Exons of PHOX2 gene were amplified and sequenced. A total of 100 normal subjects were recruited as controls.</p><p><b>RESULTS</b>Genetic linkage was found at 11q13 between D11S4151 and D11S1320 and the PHOX2A gene. DNA sequencing has identified a heterozygous mutation in the exon 2 of the gene (227T to G, N76K). The same mutation was not found in the unaffected and 100 normal controls.</p><p><b>CONCLUSION</b>A mutation of the PHOX2A gene 227T to G is responsible for the onset of congenital fibrosis of extraocular muscles type 2 in this Chinese family.</p>
Subject(s)
Female , Humans , Male , Base Sequence , Case-Control Studies , China , Fibrosis , Genetics , Homeodomain Proteins , Genetics , Molecular Sequence Data , Mutation , Ocular Motility Disorders , Genetics , Oculomotor Muscles , Congenital Abnormalities , PedigreeABSTRACT
<p><b>OBJECTIVE</b>To study the effect of plant growth regulator mepiquat chloride (DPC) on the growing development of plant and the content of active compounds in Scutellaria baicalensis.</p><p><b>METHOD</b>After spraying DPC during the seedling period, the length of taproot, fresh weight of root, diameter of taproot and the length of stem were measured. The contents of baicalin, baicalein and wogonin were determined by HPLC, respectively. Total flavonoids and scavenging DPPH were determined with ultraviolet spectrophotometry.</p><p><b>RESULT</b>After spraying DPC, fresh weight of S. baicalensis root was significant increased, and root diameter was also increased. The contents of baicalin and total flavonoids were significantly increased and baicalein and wogonin were decreased remarkably. Compared with controls, scavenging activity of ethanol extracts on DPPH free radical was no significant changed after spraying DPC.</p><p><b>CONCLUSION</b>Plant growth regulator DPC could regulate the growth on the ground and underground effectively, and could enhance the content of flavonoids compounds of S. baicalensis.</p>
Subject(s)
Chromatography, High Pressure Liquid , Piperidines , Pharmacology , Plant Growth Regulators , Pharmacology , Scutellaria baicalensis , ChemistryABSTRACT
<p><b>OBJECTIVE</b>To find out the influence of differences pruning on Lonicerea Japonicae Flos on it's yield and quality, and provide reference for reasonable pruning.</p><p><b>METHOD</b>Using different pruning treatments, the growth and yield and chlorogenic acid and galuteolin contents of Lonicerea Japonicae Flos were measured and compared. And the source and sink theory were used to interpret the rationality of the best way.</p><p><b>RESULT</b>There existed significant differences in the growth and branching and yield at differences pruning methods, but not including chlorogenic acid and galuteolin contents of Lonicerea Japonicae Flos.</p><p><b>CONCLUSION</b>The best pruning treatments is in shearing.</p>
Subject(s)
Agriculture , Methods , Drugs, Chinese Herbal , Metabolism , Reference Standards , Flowers , Chemistry , Metabolism , Lonicera , Chemistry , Metabolism , Quality ControlABSTRACT
<p><b>OBJECTIVE</b>To study the developmental phase on the growth and active compounds in Scutellaria baicalensis.</p><p><b>METHOD</b>Seeds of wild plants were collected from Laiwu and sowed in Fangshan (Beijing) and Laiwu (Shandong). Samples of aerial and underground parts were collected in five growth periods of sprouts, seedlings, flowering, seed drop and withered periods respectively. The length of taproot, fresh weight of root, diameter of taproot and the length of stem were determined. The content of active compounds and total flavonoids were determined by HPLC and ultraviolet spectrophotometry respectively. The transcripted level of PAL1, PAL2, PAL3, C4H, 4CL, CHS, GUS and UBGAT were analyzed with RT-PCR.</p><p><b>RESULT</b>The results showed that the aerial part of S. baicalensis grew quickly before flowering stage, and the underground part grew mostly between the periods of flowering and withered. In the whole growing developmental periods, the content of total flavonoids was not changed significantly, the content of baicalin was increased gradually and the content of baicalein was decreased gradually. Expression level of PAL and 4CL was the highest in withered period, CHS was increased between flowering and seed drop and decreased in withered period.</p><p><b>CONCLUSION</b>Seedlings and withered periods may be the key phase affecting the growth and active compounds in S. baicalensis.</p>
Subject(s)
Acyltransferases , Genetics , Metabolism , Chromatography, High Pressure Liquid , Coenzyme A Ligases , Genetics , Metabolism , Flavonoids , Metabolism , Flowers , Genetics , Metabolism , Gene Expression Regulation, Developmental , Gene Expression Regulation, Enzymologic , Gene Expression Regulation, Plant , Glucuronidase , Genetics , Metabolism , Glucuronosyltransferase , Genetics , Metabolism , Phenylalanine Ammonia-Lyase , Genetics , Metabolism , Plant Proteins , Genetics , Metabolism , Plant Roots , Genetics , Metabolism , Plant Stems , Genetics , Metabolism , Reverse Transcriptase Polymerase Chain Reaction , Scutellaria baicalensis , Genetics , Metabolism , Seedlings , Genetics , Metabolism , Spectrophotometry, Ultraviolet , Time Factors , Trans-Cinnamate 4-Monooxygenase , Genetics , MetabolismABSTRACT
<p><b>OBJECTIVE</b>To identify SNP in flos Lonicerae, and authenticate Lonicera japonica from its adulterants and the mixture by using bidirectional PCR amplification of specific alleles (Bi-PASA).</p><p><b>METHOD</b>SNP of L. japonica and its adulterants was identified by using ClustulW to align trnL-trnF sequences of the Lonicera genus from GenBank database. Bi-PASA primer was designed and the PCR reaction systems including annealing temperature optimized. Optimized result was performed in 84 samples to authenticate L. japonica, its adulterants and the mixture.</p><p><b>RESULT</b>When the annealing temperature was 61 degrees C, DNA from L. japonica would be amplified 468 bp whereas PCR products from all of the 9 adulterants were 324 bp. The established method also can detect 5% of intentional adulteration DNA into L. japonica.</p><p><b>CONCLUSION</b>The Bi-SPASA could authenticate L. japonica from its adulterants and the mixture.</p>
Subject(s)
Alleles , DNA Barcoding, Taxonomic , Methods , DNA, Plant , Genetics , Flowers , Genetics , Lonicera , Classification , Genetics , Plants, Medicinal , Classification , Genetics , Polymerase Chain Reaction , Methods , Polymorphism, Single Nucleotide , RNA, Transfer, Leu , Genetics , RNA, Transfer, Phe , Genetics , Reproducibility of Results , Species SpecificityABSTRACT
A FatB unigene was obtained from the transcriptome dataset of Lonicera japonica Thunb. Full-length FatB cDNA was cloned from buds of Lonicera japonica Thunb., Lonicera japonica Thunb. var. chinensis (Wats.) Bak., Lonicera hypoglauca Miq. and Lonicera dasystyla Rehd. using RT-PCR technology, and named as LJFatB, LHFatB, LJCFatB and LDFatB. The results of bioinformatic analysis showed that LJFatB, LJCFatB, LHFatB and LDFatB and Arabidopsis thaliana AtFatB had a closely relationship. Nucleotide sequences and protein secondary structure of LJFatB, LJCFatB, LHFatB and LDFatB are different and their proteins had conserved FatB substrate binding sites and catalytic activity sites. Transcriptive level of LJFatB, LJCFatB, LHFatB and LDFatB in bud was not significantly different. Therefore, LJFatB, LJCFatB, LHFatB and LDFatB could have the same biological function as AtFatB.
Subject(s)
Amino Acid Sequence , Cloning, Molecular , Computational Biology , DNA, Complementary , Genetics , Flowers , Chemistry , Genetics , Metabolism , Lonicera , Chemistry , Classification , Genetics , Metabolism , Open Reading Frames , Genetics , Phylogeny , Plant Proteins , Genetics , Metabolism , Protein Structure, Secondary , Thiolester Hydrolases , Genetics , Metabolism , Transcriptome , GeneticsABSTRACT
<p><b>OBJECTIVE</b>To study the germination property of the seeds of Achyranthes bidentata from different producing area, providing foundation for choosing the better seed resources.</p><p><b>METHOD</b>The germination rate, germination energy, germination index, vigor and the characteristics of the seeds of A. bidentata from different producing area were compared, and the relative electric conductivity was measured. The characteristics of the seed were recorded through the Anymicro DSS YT-5M microscope digital camera, and the differences were analyzed.</p><p><b>RESULT</b>Seed from Henan Boai and Hebei Anguo showed the better germination rate, germination energy, germination index and vigor.</p><p><b>CONCLUSION</b>The seeds from both Henan Boai and Hebei Anguo showed the better quality.</p>
Subject(s)
Achyranthes , Metabolism , Physiology , China , Geography , Germination , Physiology , Seeds , Metabolism , PhysiologyABSTRACT
<p><b>OBJECTIVE</b>Through analyze of shape, structure and content of effective components of Cistanche deserticola, the variation of "you cong rong" is discussed.</p><p><b>METHOD</b>The color surface, texture, the size of pith and the arrange of vascular bundle was observed with freshed, dried drugs and the transverse section, the effective component of echinacoside and acteoside was analyzed with hplc and the amylose was analyzed with ultraviolet spectrophotometry.</p><p><b>RESULT</b>The variation of "you cong rong" is obvious different with the common drug in shape and structure, the content of echinacoside is 2.5 times, acteoside is 3.8 times, amylose yield is 1.6 times and the content is 2 times of the common drugs.</p><p><b>CONCLUSION</b>"you cong rong" is an independent variation pattern of C. deserticola, it has no relationship with the ecological and geographical conditions.</p>
Subject(s)
Amylose , Chemistry , Chromatography, High Pressure Liquid , Cistanche , Chemistry , Drugs, Chinese Herbal , Chemistry , Glucosides , Chemistry , Glycosides , Chemistry , Phenols , ChemistryABSTRACT
<p><b>OBJECTIVE</b>To investigate the inductive factors of effect on Akebia trifoliata and establish culture method for A. trifoliata callus.</p><p><b>METHOD</b>To study the possible effective factors of culture condition by comparing with different explantation, nutrient medium, pH, temperature, illumination, growth substance of plant and its ratio.</p><p><b>RESULT</b>The inductivity of leaves was the highest about 87.5%, followed with the stem section and leafstalk; The inductivity of nutrient medium such as MS, B5 callus was higher than the ones like H, SH and the White callus amended one; It was found that low-grade Phvalue benefits the growth of callus. The experiment result showed that different pH showed little difference in quality. The best condition of culture was 25 degrees C in temperature.</p><p><b>CONCLUSION</b>The best culture condition for callus was the leaves as explantation. The A. trifoliata callus culture's best inductive condition was MS +2, 4-D 4.0 mg x L(-1) + NAA 1.0 mg x L(-1) + KT 1.0 mg x L(-1) (pH 5.8), cultural temperature was 25 degrees C, cultivation was dark.</p>
Subject(s)
Culture Media , Chemistry , Pharmacology , Hydrogen-Ion Concentration , Magnoliopsida , Plant Leaves , Plant Stems , Plants, Medicinal , Temperature , Tissue Culture Techniques , MethodsABSTRACT
<p><b>OBJECTIVE</b>To study the effects of Arbuscular Mycorrhizae on cultivated Atractylodes lancea.</p><p><b>METHOD</b>Pot experiment of A. lancea, with (code as AM) or without (code as CK) Glomus mosseae (GM) was conducted 5 times respectively, then the biomass, essential oil, and soil nutrition, soil organism, soil microbial were detected after A. lancea were harvested.</p><p><b>RESULT</b>(1) Mycorrhizal dependency of A. lancea was 245%, and height of individuals, numbers of leaves, leaf area, biomass of A. lancea were all higher in AM than in CK (P < 0.05). (2) GC-MS analysis with cluster analysis and principal components analysis showed that there were no differences in essential oil of A. lancea between AM and CK. (T3) Total N, available N, available P and available K in AM soil were all lower than in CK soil. (4) GC-MS analysis showed organic matters changed differenly in AM soil and CK soil, components 5,6 in AM soil were higher than that in CK soil, but component 9, 10, 11 were lower in AM soil than that in CK soil. (5) Biolog detect showed AWCD of AM soil microbe were higher than that of CK soil throughout the incubation, and AWCD of the former was 0.66, and the later was 0.46 after 192 h incubation. and t-test showed, Shannon seven indices and McIntosh'seven indices were same both at 72 h and 192 h, and diversity indices of Shannon and McIntosh were also same at 72 h, but AM soil microbe were higher than CK soil microbe at 168 h (P < 0.05).</p><p><b>CONCLUSION</b>AM could promote nutrition uptake, improve the function diversity and activity of microbe in rhizosphere of A. lancea, influence the composition of the organic matter, that lead the growth of A. lancea, but not to the quality.</p>
Subject(s)
Atractylodes , Metabolism , Microbiology , Mycorrhizae , Physiology , Nitrogen , Oils, Volatile , Metabolism , Phosphorus , Plants, Medicinal , Metabolism , Microbiology , Potassium , Soil , Soil MicrobiologyABSTRACT
<p><b>OBJECTIVE</b>To provide reference for breeding Scutellaria baicalensis from different germplasms,and to explore their genetic diversities and different strains.</p><p><b>METHOD</b>The RAPD method was applied to the study on S. baicalensis from different germplasms by use of 14 random primers about 10 bp, and SAPD-analysis of 34 S. baicalensis from different germplasms was carried out by using the method of withingroups-linkage in SPSS 10.0.</p><p><b>RESULTS</b>14 among 115 primers were selected to amplify about 165 segments of DNA. Among them, 132 segments of DNA, 80.0% of the total, can represent genetic of diversities of S. baicalensis. According to RAPD analysis, 34 germplasms of S. baicalensis were classified into A, B, C and D categories.</p><p><b>CONCLUSION</b>S. baicalensis from different germplasms shows abundant genetic diversities. Germplasms from Shandong like Mengyin 3, Menyin 2 and Pingyi have close distance (0.315) in genetic background, which can be chosen for breeding of cultivated. Though genetic characters are similar in the morphology, the geological distribution of S. baicalensis and its morphology have not certain correlation. The complex genetic background of S. baicalensis indicate that the work of the selective breeding and management for breeding of S. baicalensis have to be strengthened.</p>
Subject(s)
Breeding , Cluster Analysis , DNA Primers , Genetics , DNA, Plant , Genetics , Ecosystem , Genetic Variation , Phylogeny , Plant Leaves , Genetics , Plants, Medicinal , Genetics , Random Amplified Polymorphic DNA Technique , Methods , Scutellaria baicalensis , GeneticsABSTRACT
<p><b>OBJECTIVE</b>To provide reference for breeding of cultivated ginseng by researching the genetic diversities among different strains.</p><p><b>METHOD</b>To make up the systematic diagram of genetic relationship by calculating the proximity coefficient with SPSS 10.0 software and clustered by between-groups linkage method.</p><p><b>RESULT</b>The selected 18 random primers used in PCR amplification to produce 145 bands in 17 samples, among which 53 bands (36.5%) are polymorphic. The results of cluster analysis show that the genetic relationship between different strains of Da-maya is closer than that of Er-maya, which proves that it is feasible to differentiate the cultivated groups in molecular level on outside character.</p><p><b>CONCLUSION</b>RAPD is a favorable molecular marker to assist ginseng breeding.</p>