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2014 | 83 | 2 |

Tytuł artykułu

Isolation of biosynthesis related transcripts of 2,3,5,4'-tetrahydroxy stilbene-2-O-beta-D-glucoside from Fallopia multiflora by suppression subtractive hybridization

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
2,3,5,4'-tetrahydroxy stilbene-2-O-ß-D-glucoside (THSG) exerts multiple pharmacodynamic actions, found in Fallopia multiflora, but the biosynthesis pathway of THSG is still unclear. To clear this ambiguity, we constructed suppression subtractive hybridization (SSH) libraries to screen the genes involved in THSG biosynthesis from two F. multiflora varieties, which vary significantly in THSG content. Twelve non-redundant differentially expressed sequence tags were obtained and the full lengths of 4 unreported fragments were amplified by rapid amplification of cDNA ends. We totally got 7 fulllength transcripts, and all of them were aligned to the transcriptome and digital gene expression tag profiling database of four F. multiflora tissues (root, stem and leaf from Deqing F. multiflora and another root from Chongqing F. multiflora; data unpublished) using local BLAST. The results showed that there was a significant, organ specific difference in the expression of fragments and full-length sequences. All the sequences were annotated by aligning to nucleotide and protein databases. Kyoto Encyclopedia of Genes and Genomes pathway analysis indicated that THSG biosynthesis was correlated with multiple life activities.

Wydawca

-

Rocznik

Tom

83

Numer

2

Opis fizyczny

p.147-157,fig.,ref.

Twórcy

autor
  • School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, People’s Republic of China
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, People’s Republic of China
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, People’s Republic of China
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People’s Republic of China
autor
  • School of Life Sciences, Guangzhou University, Guangzhou 510006, People’s Republic of China

Bibliografia

  • 1. Steele ML, Truong J, Govindaraghavan S, Ooi L, Sucher NJ, Münch G. Cytoprotective properties of traditional Chinese medicinal herbalextracts in hydrogen peroxide challenged human U373 astroglia cells.Neurochem Int. 2013;62(5):522–529. http://dx.doi.org/10.1016/j.neuint.2012.08.018
  • 2. Xie W, Zhao Y, Du L. Emerging approaches of traditional Chinese medicine formulas for the treatment of hyperlipidemia. J Ethnopharmacol.2012;140(2):345–367. http://dx.doi.org/10.1016/j.jep.2012.01.027
  • 3. Jang JY, Kim HN, Kim YR, Choi YW, Choi YH, Lee JH, et al. Hexane extract from Polygonum multiflorum attenuates glutamate-inducedapoptosis in primary cultured cortical neurons. J Ethnopharmacol.2013;145(1):261–268. http://dx.doi.org/10.1016/j.jep.2012.10.061
  • 4. Wang M, Zhao R, Wang W, Mao X, Yu J. Lipid regulation effects of Polygoni Multiflori Radix, its processed products and its majorsubstances on steatosis human liver cell line L02. J Ethnopharmacol.2012;139(1):287–293. http://dx.doi.org/10.1016/j.jep.2011.11.022
  • 5. Lv G, Lou Z, Chen S, Gu H, Shan L. Pharmacokinetics and tissue distribution of 2,3,5,4'-tetrahydroxystilbene-2-O-β-D-glucoside fromtraditional Chinese medicine Polygonum multiflorum following oraladministration to rats. J Ethnopharmacol. 2011;137(1):449–456. http://dx.doi.org/10.1016/j.jep.2011.05.049
  • 6. Zhang JK, Yang L, Meng GL, Fan J, Chen JZ, He QZ, et al. Protective effect of tetrahydroxystilbene glucoside against hydrogen peroxide-induced dysfunction and oxidative stress in osteoblastic MC3T3-E1 cells. Eur J Pharmacol. 2012;689(1–3):31–37. http://dx.doi. org/10.1016/j.ejphar.2012.05.045
  • 7. Yao WJ, Fan WJ, Huang C, Zhong H, Chen XF, Zhang W. Proteomic analysis for anti-atherosclerotic effect of tetrahydroxystilbene glucoside in rats. Biomed Pharmacother. 2013;67(2):140–145. http://dx.doi.org/10.1016/j.biopha.2012.10.007
  • 8. Sun FL, Zhang L, Zhang RY, Li L. Tetrahydroxystilbene glucoside protects human neuroblastoma SH-SY5Y cells against MPP+-induced cytotoxicity. Eur J Pharmacol. 2011;660(2/3):283–290. http://dx.doi. org/10.1016/j.ejphar.2011.03.046
  • 9. Chong J, Poutaraud A, Hugueney P. Metabolism and roles of stilbenes in plants. Plant Sci. 2009;177(3):143–155. http://dx.doi.org/10.1016/j.plantsci.2009.05.012
  • 10. Hartmann T. From waste products to ecochemicals: fifty years research of plant secondary metabolism. Phytochemistry. 2007;68(22–24):2831–2846. http://dx.doi.org/10.1016/j.phytochem.2007.09.017
  • 11. Sheng SJ, Liu ZY, Zhao W, Shao L, Zhao SJ. Molecular analysis of a type III polyketide synthase gene in Fallopia multiflora. Biologia (Bratisl.).2010;65(6):939–946. http://dx.doi.org/10.2478/s11756-010-0113-8
  • 12. Shao L, Zhao SJ, Cui TB, Liu ZY, Zhao W. 2,3,5,4'-tetrahydroxystilbene- 2-O-β-D-glycoside biosynthesis by suspension cells cultures ofPolygonum multiflorum Thunb and production enhancement by methyljasmonate and salicylic acid. Molecules. 2012;17(12):2240–2247. http://dx.doi.org/10.3390/molecules17022240
  • 13. Peng T, Zhu XF, Fan QJ, Sun PP, Liu JH. Identification and characterization of low temperature stress responsive genes in Poncirus trifoliataby suppression subtractive hybridization. Gene. 2012;492(1):220–228.http://dx.doi.org/10.1016/j.gene.2011.10.025
  • 14. Gao M, Wang Q, Wan R, Fei Z, Wang X. Identification of genes differentially expressed in grapevine associated with resistance to Elsinoe ampelina through suppressive subtraction hybridization. Plant Physiol Biochem. 2012;58:253–268. http://dx.doi.org/10.1016/j. plaphy.2012.07.009
  • 15. Pimentel P, Salvatierra A, Moya-León MA, Herrera R. Isolation of genes differentially expressed during development and ripening ofFragaria chiloensis fruit by suppression subtractive hybridization. JPlant Physiol. 2010;167(14):1179–1187. http://dx.doi.org/10.1016/j.jplph.2010.03.006
  • 16. Wang YS, Gao LP, Wang ZR, Liu YJ, Sun ML, Yang DQ, et al. Lightinduced expression of genes involved in phenylpropanoid biosynthetic pathways in callus of tea [Camellia sinensis (L.) O. Kuntze]. Sci Hortic. 2012;133:72–83. http://dx.doi.org/10.1016/j.scienta.2011.10.017
  • 17. Fukushima EO, Seki H, Ohyama K, Ono E, Umemoto N, Mizutani M, et al. CYP716A subfamily members are multifunctional oxidases intriterpenoid biosynthesis. Plant Cell Physiol. 2011;52(12):2050–2061.http://dx.doi.org/10.1093/pcp/pcr146
  • 18. Seki H, Sawai S, Ohyama K, Mizutani M, Ohnishi T, Sudo H, et al. Triterpene functional genomics in licorice for identification of CYP72A154 involved in the biosynthesis of glycyrrhizin. Plant Cell. 2011;23(11):4112–4123. http://dx.doi.org/10.1105/tpc.110.082685
  • 19. Carelli M, Biazzi E, Panara F, Tava A, Scaramelli L, Porceddu A, et al. Medicago truncatula CYP716A12 is a multifunctional oxidaseinvolved in the biosynthesis of hemolytic saponins. Plant Cell.2011;23(8):3070–3081. http://dx.doi.org/10.1105/tpc.111.087312

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-8dc281dc-8c91-4b84-99a6-73f6a568cdf4
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