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劳氏肉瘤病毒长末端重复序列的转录活性与一种因子在体外与上游CCAAT框的结合相关。

Transcriptional activity of the Rous sarcoma virus long terminal repeat correlates with binding of a factor to an upstream CCAAT box in vitro.

作者信息

Greuel B T, Sealy L, Majors J E

机构信息

Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Virology. 1990 Jul;177(1):33-43. doi: 10.1016/0042-6822(90)90457-3.

Abstract

The avian nuclear protein, enhancer factor 1 (EF1), binds specifically to the long terminal repeat (LTR) of Rous sarcoma virus (RSV) in a region that has been implicated in enhancer/promoter function. We have characterized the in vitro binding properties of this factor from chick embryo nuclear extracts by methylation interference/protection foot-printing of the wild-type LTR and also by gel electrophoretic mobility shift assays performed on a series of LTR mutants. We find that the inverted CCAAT pentanucleotide located at position -129 is essential for EF1 binding in vitro. Nucleotides flanking this element exert a smaller effect on binding. Linker-substitution and point mutations which reduce EF1 binding to this site in vitro also reduce promoter activity in transiently transfected cells. EF1 also binds with lower affinity to another inverted CCAAT box at position -65, an element which we show is also essential for transcriptional activity of the RSV LTR. We conclude, therefore, that EF1 is a CCAAT box-binding factor which is involved in the activation of RSV transcription in avian cells. Furthermore, we show that EF1 can recognize the CCAAT boxes of several other promoters in which the functional importance of this pentanucleotide has been established.

摘要

禽类核蛋白增强子因子1(EF1)特异性结合劳氏肉瘤病毒(RSV)长末端重复序列(LTR)中一个与增强子/启动子功能有关的区域。我们通过对野生型LTR进行甲基化干扰/保护足迹分析,以及对一系列LTR突变体进行凝胶电泳迁移率变动分析,对来自鸡胚核提取物的该因子的体外结合特性进行了表征。我们发现位于-129位的反向CCAAT五核苷酸对于EF1体外结合至关重要。该元件两侧的核苷酸对结合的影响较小。在体外降低EF1与该位点结合的接头取代和点突变,也会降低瞬时转染细胞中的启动子活性。EF1还以较低亲和力结合位于-65位的另一个反向CCAAT框,我们表明该元件对于RSV LTR的转录活性也至关重要。因此,我们得出结论,EF1是一种CCAAT框结合因子,参与禽类细胞中RSV转录的激活。此外,我们表明EF1可以识别其他几个启动子的CCAAT框,其中该五核苷酸的功能重要性已得到证实。

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