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ETS 结构域蛋白对淋巴特异性免疫球蛋白 μ 重链基因增强子的调控

Regulation of lymphoid-specific immunoglobulin mu heavy chain gene enhancer by ETS-domain proteins.

作者信息

Nelsen B, Tian G, Erman B, Gregoire J, Maki R, Graves B, Sen R

机构信息

Rosenstiel Research Center, Brandeis University, Waltham, MA 02254.

出版信息

Science. 1993 Jul 2;261(5117):82-6. doi: 10.1126/science.8316859.

Abstract

The enhancer for the immunoglobulin mu heavy chain gene (IgH) activates a heterologous gene at the pre-B cell stage of B lymphocyte differentiation. A lymphoid-specific element, microB, is necessary for enhancer function in pre-B cells. A microB binding protein is encoded by the PU.1/Spi-1 proto-oncogene. Another sequence element, microA, was identified in the mu enhancer that binds the product of the ets-1 proto-oncogene. The microA motif was required for microB-dependent enhancer activity, which suggests that a minimal B cell-specific enhancer is composed of both the PU.1 and Ets-1 binding sites. Co-expression of both PU.1 and Ets-1 in nonlymphoid cells trans-activated reporter plasmids that contained the minimal mu enhancer. These results implicate two members of the Ets family in the activation of IgH gene expression.

摘要

免疫球蛋白μ重链基因(IgH)的增强子在B淋巴细胞分化的前B细胞阶段激活一个异源基因。一个淋巴特异性元件,即微型B,对于前B细胞中的增强子功能是必需的。微型B结合蛋白由PU.1/Spi-1原癌基因编码。在μ增强子中鉴定出另一个序列元件,即微型A,它结合ets-1原癌基因的产物。微型A基序对于微型B依赖的增强子活性是必需的,这表明最小的B细胞特异性增强子由PU.1和Ets-1结合位点组成。PU.1和Ets-1在非淋巴细胞中共表达可反式激活含有最小μ增强子的报告质粒。这些结果表明Ets家族的两个成员参与了IgH基因表达的激活。

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