Moore J T, McKee D D, Slentz-Kesler K, Moore L B, Jones S A, Horne E L, Su J L, Kliewer S A, Lehmann J M, Willson T M
Department of Molecular Sciences, Glaxo Wellcome Research and Development, Research Triangle Park, North Carolina 27709, USA.
Biochem Biophys Res Commun. 1998 Jun 9;247(1):75-8. doi: 10.1006/bbrc.1998.8738.
Multiple transcripts which arise from the human estrogen receptor beta (ER beta) gene have been characterized. Three full length isoforms of the hER beta gene, designated hER beta 1-3, were identified in a testis cDNA library. An additional two isoforms, designated hER beta 4 and hER beta 5, were identified by PCR amplification from testis cDNA and from the MDA-MB 435 cell line. hER beta 1 corresponds to the previously described hER beta. All five isoforms diverge at a common position within the predicted helix 10 of the ligand binding domain of hER beta, with nucleotide sequences consistent with differential exon usage. The hER beta isoform mRNAs displayed a differential pattern of expression in human tissues and in tumor cell lines when analyzed by RT-PCR. Further characterization of the three full length isoforms, hER beta 1-3, by in vitro band shift studies indicated that the isoforms were able to form DNA-binding homodimers and heterodimers with each other and with the ER alpha subtype.
已对源自人类雌激素受体β(ERβ)基因的多种转录本进行了表征。在睾丸cDNA文库中鉴定出hERβ基因的三种全长异构体,命名为hERβ1 - 3。另外两种异构体,命名为hERβ4和hERβ5,是通过从睾丸cDNA和MDA - MB 435细胞系进行PCR扩增鉴定出来的。hERβ1对应于先前描述的hERβ。所有五种异构体在hERβ配体结合域预测的螺旋10内的一个共同位置处存在差异,其核苷酸序列与外显子使用差异一致。通过RT - PCR分析时,hERβ异构体mRNA在人类组织和肿瘤细胞系中呈现出不同的表达模式。通过体外凝胶迁移实验对三种全长异构体hERβ1 - 3进行的进一步表征表明,这些异构体能够彼此之间以及与ERα亚型形成DNA结合同二聚体和异二聚体。