Differential Display Analysis of Gene Expression Induced under DCA Treatment in Rat Liver

  • Received : 1996.01.29
  • Published : 1996.05.31

Abstract

The expression of genes induced by Dichloroacetate (DCA) treatment was analyzed by mRNA differential display. Purified total RNAs from rat liver treated with saline or DCA (100 mg/100 g b.w.) were reverse transcribed by using a set of oligonucleotide primers. The PCR products were resolved on a denaturing sequencing gel. PCR band representing mRNA expressed specifically in DCA-treated liver was excised and reamplified by PCR. A 120-bp c-DNA clone named IC1 was isolated and the DNA sequence of IC1 was analyzed. IC1 revealed 50% homology with 3' end of a mouse fibroblast growth factor mRNA This result indicates that DCA induces the expression of a gene which has a 50% homology with a Mouse fibroblast growth factor, and expression of this gene might be involved in non genotoxic process caused by DCA.

Keywords

References

  1. Toxicology v.63 Bull, R.J.;Sanchez, I.M.;Nelson, M.A.;Larson, J.L.;Lansing, A. https://doi.org/10.1016/0300-483X(90)90195-M
  2. Toxicol. Appl. Pharmacol. v.101 DeAngelo, A.B.;Daniel, F.B.;McMillan, L.;Wemsing, P.;Savage, R.E. Jr. https://doi.org/10.1016/0041-008X(89)90277-9
  3. Carcinogenesis v.8 Elliot, B.M.;Elcombe, C.R. https://doi.org/10.1093/carcin/8.9.1213
  4. Ann. Rev. Pharmacol. Toxicol. v.31 Grasso, P.;Sharrat, M. https://doi.org/10.1146/annurev.pa.31.040191.001345
  5. Chem. Pharm. Bull. v.40 Hayashi, Y.;Yamamoto, I.;Gohda, E. https://doi.org/10.1248/cpb.40.452
  6. Am. J. Clin. Nutr. v.33 Herbert, V.;Gardner, A.;Coleman, N. https://doi.org/10.1093/ajcn/33.2.179
  7. Nucl. Acids Res. v.19 Kovalic, J.H.;Kwak, J.H.;Weisblum, B. https://doi.org/10.1093/nar/19.16.4560
  8. Ann. Inter. Med. v.92 Kreisberg, R.A. https://doi.org/10.7326/0003-4819-92-2-227
  9. Science v.257 Liang, P.;Pardee, A.B.
  10. Nucl. Acids. Res. v.21 Liang, P.;Averboukh, L.;Pardee, A.B. https://doi.org/10.1093/nar/21.14.3269
  11. Nucl. Acids Res. v.22 Liang, P.;Zhu, W.;Zhang, X.;Guo, Z.;O'Connel, R.P.;Averboukh, L.;Wang, F.;Pardee, A.B. https://doi.org/10.1093/nar/22.25.5763
  12. Am. J. Physiol. v.261 Nicholl, T.A.;Lopaschuk, G.D.;McNeill, J.H.
  13. FASEB J. v.8 Nishio, Y.;Aiello, L.P.;King, G.L. https://doi.org/10.1096/fasebj.8.1.8299882
  14. Mol. Cell. Biol. v.11 Owens, G.P.;Hahn, W.E.;Cohen, J.J. https://doi.org/10.1128/MCB.11.8.4177
  15. Gut v.16 Record, C.O.;Iles, R.A.;Cohen, R.D.;Williams, R.
  16. Anesthesiol. v.77 Shangraw, R.E.;Winter, R. https://doi.org/10.1097/00000542-199209001-00235
  17. Proc. Natl. Acad. Sci. USA v.92 Shen, R.;Su, Z.;Olsson, C.A.;Fisher, P.B. https://doi.org/10.1073/pnas.92.15.6778
  18. Diabetic Care v.15 Stacpoole, P.W.;Greene, Y.J. https://doi.org/10.2337/diacare.15.6.785
  19. Metabolism v.38 Stacpoole, P.W. https://doi.org/10.1016/0026-0495(89)90051-6
  20. Cell v.16 John, T.P.;Davis, R.W. https://doi.org/10.1016/0092-8674(79)90020-5
  21. Gene v.161 Tseng, T.C.;Tsai, T.H.;Lue, M.Y.;Lee, H. https://doi.org/10.1016/0378-1119(95)00243-Y
  22. Surgery v.110 Wolfe, R.R.;Jahoor, F.;Herndon, P.N.;Miyoshi, H.