Lieberson R, Giannini S L, Birshtein B K, Eckhardt L A
Department of Biological Sciences, Columbia University, New York, NY 10027.
Nucleic Acids Res. 1991 Feb 25;19(4):933-7. doi: 10.1093/nar/19.4.933.
A tissue-specific enhancer (E mu) lies between the joining (JH) and mu constant region (C mu) gene segments of the immunoglobulin heavy chain (IgH) locus. Since mouse endogenous IgH genes are efficiently transcribed in its absence, the normal function of this enhancer remains ill-defined. Recently, another lymphoid-specific enhancer of equal strength has been identified 3' of the rat IgH locus. We have isolated an analogous sequence from mouse and have mapped it 12.5 kb 3' of the 3'-most constant region gene (C alpha-membrane) of the BALB/c mouse locus. The mouse and rat sequences are 82% homologous and share with other enhancers several DNA sequence motifs capable of binding protein. However, in transient transfection assays, the mouse sequence behaves as a weaker enhancer. The role of this distant element in the expression of endogenous IgH genes, both in E mu-deficient, Ig-producing cell lines and during normal B cell development, is discussed.
一个组织特异性增强子(Eμ)位于免疫球蛋白重链(IgH)基因座的连接(JH)和μ恒定区(Cμ)基因片段之间。由于小鼠内源性IgH基因在其缺失时仍能有效转录,该增强子的正常功能仍不明确。最近,在大鼠IgH基因座的3'端发现了另一个强度相当的淋巴样特异性增强子。我们从小鼠中分离出了一个类似序列,并将其定位在BALB/c小鼠基因座最3'端恒定区基因(Cα-膜)的3'端12.5 kb处。小鼠和大鼠的序列有82%的同源性,并与其他增强子共享几个能够结合蛋白质的DNA序列基序。然而,在瞬时转染实验中,小鼠序列表现为较弱的增强子。本文讨论了这个远端元件在Eμ缺陷的Ig产生细胞系以及正常B细胞发育过程中内源性IgH基因表达中的作用。