Objective To investigate a rapid and sensitive scr eening method for detecting estrogenic compounds in enviromnental hormone.
Methods Both expression plasmid pcDNA31.1-ER and repor ter plasmid pGL3-tk-ERE were constructed by inserting cDNA of human estrogen receptor-α(ER-α)into plasmid pcDNA31.1 and estrogen receptor response element(ERE)into reporter plasmid pGL3-tk, respectively.After cotransfection the two plasmids into Hela cells, the luciferase activity induced by 17-β-estradiol(E2)or Bisphenol A(BPA)through the interaction of ER with ERE were detected.
Results the activity of enzyme regulated by ERE in the presence of E2 and BPA were linearly correlated with the concentration of E2 and BPA within a certain dose range.
Conclusion this method was suitable for detection of estrogen and estrogenic compounds.With further development, it would become a rapid and efficient routine method for detection of estrogenic compounds in the environmental hormone.