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非红细胞系细胞中珠蛋白启动子的反式激活

trans-Activation of a globin promoter in nonerythroid cells.

作者信息

Evans T, Felsenfeld G

机构信息

Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland 20892.

出版信息

Mol Cell Biol. 1991 Feb;11(2):843-53. doi: 10.1128/mcb.11.2.843-853.1991.

Abstract

We show that expression in fibroblasts of a single cDNA, encoding the erythroid DNA-binding protein Eryf1 (GF-1, NF-E1), very efficiently activates transcription of a chicken alpha-globin promoter, trans-Activation in these cells occurred when Eryf1 bound to a single site within a minimal globin promoter. In contrast, efficient activation in erythroid cells required multiple Eryf1 binding sites. Our results indicate that mechanisms exist that are capable of modulating the trans-acting capabilities of Eryf1 in a cell-specific manner, without affecting DNA binding. The response of the minimal globin promoter to Eryf1 in fibroblasts was at least as great as for optimal constructions in erythroid cells. Therefore, the assay provides a very simple and sensitive system with which to study gene activation by a tissue-specific factor.

摘要

我们发现,在成纤维细胞中表达单一的编码红系DNA结合蛋白Eryf1(GF-1,NF-E1)的cDNA,能非常有效地激活鸡α-珠蛋白启动子的转录。当Eryf1与最小珠蛋白启动子内的单个位点结合时,这些细胞中就会发生反式激活。相比之下,在红系细胞中高效激活则需要多个Eryf1结合位点。我们的结果表明,存在能够以细胞特异性方式调节Eryf1反式作用能力而不影响DNA结合的机制。最小珠蛋白启动子对成纤维细胞中Eryf1的反应至少与对红系细胞中最佳构建体的反应一样强烈。因此,该检测提供了一个非常简单且灵敏的系统,用于研究组织特异性因子对基因的激活作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3be6/359736/5d26f12b70e2/molcellb00137-0271-a.jpg

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