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分离出一种候选阻遏物/激活物NF-E1(YY-1,δ),它能与免疫球蛋白κ轻链3'增强子及免疫球蛋白重链μ E1位点结合。

Isolation of a candidate repressor/activator, NF-E1 (YY-1, delta), that binds to the immunoglobulin kappa 3' enhancer and the immunoglobulin heavy-chain mu E1 site.

作者信息

Park K, Atchison M L

机构信息

Department of Animal Biology, University of Pennsylvania, School of Veterinary Medicine, Philadelphia 19104.

出版信息

Proc Natl Acad Sci U S A. 1991 Nov 1;88(21):9804-8. doi: 10.1073/pnas.88.21.9804.

DOI:10.1073/pnas.88.21.9804
PMID:1946405
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC52809/
Abstract

We have determined that the developmental control of immunoglobulin kappa 3' enhancer (kappa E3') activity is the result of the combined influence of positive- and negative-acting elements. We show that a central core in the kappa E3' enhancer is active at the pre-B-cell stage but is repressed by flanking negative-acting elements. The negative-acting sequences repress enhancer activity in a position- and orientation-independent manner at the pre-B-cell stage. We have isolated a human cDNA clone encoding a zinc finger protein (NF-E1) that binds to the negative-acting segment of the kappa E3' enhancer. This protein also binds to the immunoglobulin heavy-chain enhancer mu E1 site. NF-E1 is encoded by the same gene as the YY-1 protein, which binds to the adeno-associated virus P5 promoter. NF-E1 is also the human homologue of the mouse delta protein, which binds to ribosomal protein gene promoters. The predicted amino acid sequence of this protein contains features characteristic of transcriptional activators as well as transcriptional repressors. Cotransfection studies with this cDNA indicate that it can repress basal promoter activity. The apparent dual function of this protein is discussed.

摘要

我们已经确定,免疫球蛋白κ 3'增强子(κ E3')活性的发育控制是正负作用元件共同影响的结果。我们发现,κ E3'增强子的一个中央核心在前B细胞阶段具有活性,但受到侧翼负作用元件的抑制。这些负作用序列在前B细胞阶段以与位置和方向无关的方式抑制增强子活性。我们分离出了一个编码锌指蛋白(NF-E1)的人类cDNA克隆,该蛋白与κ E3'增强子的负作用片段结合。这种蛋白还与免疫球蛋白重链增强子μ E1位点结合。NF-E1与YY-1蛋白由同一基因编码,YY-1蛋白与腺相关病毒P5启动子结合。NF-E1也是小鼠δ蛋白的人类同源物,δ蛋白与核糖体蛋白基因启动子结合。该蛋白的预测氨基酸序列包含转录激活因子和转录抑制因子的特征。用该cDNA进行的共转染研究表明,它可以抑制基础启动子活性。本文讨论了这种蛋白明显的双重功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/2fd57f85e526/pnas01071-0441-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/57d0ece32806/pnas01071-0440-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/e995547bd2b7/pnas01071-0441-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/90184605d862/pnas01071-0441-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/2fd57f85e526/pnas01071-0441-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/57d0ece32806/pnas01071-0440-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/e995547bd2b7/pnas01071-0441-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/90184605d862/pnas01071-0441-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d3e/52809/2fd57f85e526/pnas01071-0441-c.jpg

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