GC-rich promoter elements maximally confers estrogen-induced transactivation of LRP16 gene through ERalpha/Sp1 interaction in MCF-7 cells

• Published in: The Journal of steroid biochemistry and molecular biology 2008-03, Vol.109 (1-2), p.47-56
• Main Authors: Han, Wei Dong, Si, Yi Ling, Zhao, Ya Li, Li, Qi, Wu, Zhi Qiang, Hao, Hao Jie, Song, Hai Jing
• Format: Article
• Language: English
• Subjects: Base Sequence; Binding Sites - genetics; Breast Neoplasms - genetics; Breast Neoplasms - metabolism; Cell Line, Tumor; DNA, Neoplasm - genetics; DNA, Neoplasm - metabolism; Estradiol - pharmacology; Estrogen Receptor alpha - metabolism; Female; GC Rich Sequence; HeLa Cells; Humans; Molecular Sequence Data; Neoplasm Proteins - genetics; Promoter Regions, Genetic; RNA, Small Interfering - genetics; Sp1 Transcription Factor - antagonists & inhibitors; Sp1 Transcription Factor - genetics; Sp1 Transcription Factor - metabolism; Transcriptional Activation - drug effects
• ISSN: 0960-0760
• DOI: 10.1016/j.jsbmb.2007.12.009

LRP16 gene has been characterized as an estrogen-responsive gene. One 1/2ERE/GC-rich site was previously identified to be indispensable for -676/-214 (region A) fragment within LRP16 regulatory region to confer E2 action. Here, we report that -213/-24 fragment (region B) has higher E2-responsiveness than that of region A in MCF-7 cells, but not in HeLa cells. Deletion and mutation analyses of region B showed that multiple GC-sites are involved in the E2-stimulated response and one 30-bp fragment (-213 to -184 bp) is essential for conferring maximum E2-responsiveness. Results from the cotransfection assays containing Sp1-siRNA revealed that Sp1 is required for the basal transcription activity and E2-responsiveness of both regions A and B. Northern blot analysis demonstrated that inhibition of Sp1 in MCF-7 cells not only decreased the basal expression of LRP16, but markedly impaired its upregulation by E2. Results from gel mobility shift assays exhibited the direct binding of Sp1 protein to the 28-bp fragment (-211 to -184 bp), which was enhanced by the ERalpha titer. Moreover, the functional interaction of ERalpha and Sp1 proteins in the presence of E2 at the GC-rich sites in region B was confirmed by chromatin immunoprecipitation (ChIP) assays. In general, these results demonstrate that GC-rich sites in the proximal promoter of LRP16 gene are sufficient for E2 activation of LRP16 and the -213/-184 fragment containing only one GC site is essential for the maximal induction in MCF-7 cells. We also provide a model for Sp1-dependent regulation of genes by E2 through GC-rich motifs.