Perez-Mutul J, Macchi M, Wasylyk B
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Faculté de Médecine, Strasbourg, France.
Nucleic Acids Res. 1988 Jul 11;16(13):6085-96. doi: 10.1093/nar/16.13.6085.
We have investigated the role of sequence motifs in the immunoglobulin heavy chain (IgH) enhancer on its activity in myeloma and fibroblast cell-lines. In transient transfection assays the transcription stimulatory activity of the enhancer is decreased in myeloma cells by mutating the E motifs 1, 2 and 3, the core motifs C1, C2, C3 and the octamer motif (OC) and in fibroblasts by mutating E2, E3, and C2. Our results suggest that transcription factors binding to E1, C1, C3 and OC contribute in a positive manner to the tissue specificity of the IgH enhancer.
我们研究了免疫球蛋白重链(IgH)增强子中的序列基序对其在骨髓瘤和成纤维细胞系中活性的作用。在瞬时转染实验中,通过突变E基序1、2和3、核心基序C1、C2、C3以及八聚体基序(OC),骨髓瘤细胞中增强子的转录刺激活性降低;通过突变E2、E3和C2,成纤维细胞中增强子的转录刺激活性降低。我们的结果表明,与E1、C1、C3和OC结合的转录因子对IgH增强子的组织特异性有正向作用。