Efficient knock-down of estrogen receptor alpha: application of recombinant adenovirus vectors for delivery of short hairpin RNA-0

Abstract

<p><b>Copyright information:</b></p><p>Taken from "Efficient knock-down of estrogen receptor alpha: application of recombinant adenovirus vectors for delivery of short hairpin RNA"</p><p>BMC Biotechnology 2006;6():11-11.</p><p>Published online 28 Feb 2006</p><p>PMCID:PMC1403768.</p><p>Copyright © 2006 Krom et al; licensee BioMed Central Ltd.</p>hERα_1103, or pSUPER- shERα_tandem. Subsequently, the cells were treated 24 hours with 10M 17-β-estradiol. Luciferase activity was measured 48 hours after transfection and after correction for LacZ expression, represented as the mean (n = 3) ± SD relative to the transfection with pSUPER-empty. (A) Endogenous mouse ERα mediated transcription in EOMA, H5V and MXT cells after introducing pSUPER +/- shERα. (B) The 19-nt target-recognition sequence of ERα_1395 contains one mismatch with human ERα and five mismatches with the mouse ERβ sequence. (C) ERα mediated transcription in EOMA cells after over expression of either mouse ERα- or human ERα-expression vectors in presence of pSUPER empty or pSUPER shERα_1395 (D) Western blot analysis of H5V cells co-transfected with pCMV-mERα and pSUPER-empty or pSUPER-shERα_1395. The lysates were analysed by immunoblotting (insert-photo) with anti-mouse ERα and anti-p38. The intensity of the bands was quantified and normalized to cells transfected with pSUPER-empty. The relative ERα protein levels are presented (bar-diagram) as mean (n = 3) +/- SD