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一种RNA结合蛋白与猿猴病毒40晚期聚腺苷酸化信号下游元件的功能重要结构域特异性相互作用。

An RNA-binding protein specifically interacts with a functionally important domain of the downstream element of the simian virus 40 late polyadenylation signal.

作者信息

Qian Z W, Wilusz J

机构信息

Department of Microbiology and Molecular Genetics, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark 07103.

出版信息

Mol Cell Biol. 1991 Oct;11(10):5312-20. doi: 10.1128/mcb.11.10.5312-5320.1991.

Abstract

We have identified an RNA-binding protein which interacts with the downstream element of the simian virus 40 late polyadenylation signal in a sequence-specific manner. A partially purified 50-kDa protein, which we have named DSEF-1, retains RNA-binding specificity as assayed by band shift and UV cross-linking analyses. RNA footprinting assays, using end-labeled RNA ladder fragments in conjunction with native gel electrophoresis, have identified the DSEF-1 binding site as 5'-GGGGGAGGUGUGGG-3'. This 14-base sequence serves as an efficient DSEF-1 binding site when placed within a GEM4 polylinker-derived RNA. Finally, the DSEF-1 binding site restored efficient in vitro 3' end processing to derivatives of the simian virus 40 late polyadenylation signal in which it substituted for the entire downstream region. DSEF-1, therefore, may be a sequence-specific binding factor which regulates the efficiency of polyadenylation site usage.

摘要

我们已鉴定出一种RNA结合蛋白,它以序列特异性方式与猿猴病毒40晚期聚腺苷酸化信号的下游元件相互作用。一种部分纯化的50 kDa蛋白,我们将其命名为DSEF-1,通过凝胶迁移和紫外线交联分析检测,它保留了RNA结合特异性。使用末端标记的RNA梯状片段结合天然凝胶电泳进行的RNA足迹分析,已确定DSEF-1结合位点为5'-GGGGGAGGUGUGGG-3'。当该14碱基序列置于GEM4多克隆位点衍生的RNA中时,它可作为有效的DSEF-1结合位点。最后,DSEF-1结合位点恢复了对猿猴病毒40晚期聚腺苷酸化信号衍生物的高效体外3'末端加工,在这些衍生物中它取代了整个下游区域。因此,DSEF-1可能是一种调节聚腺苷酸化位点使用效率的序列特异性结合因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b2b/361594/4767545f8b52/molcellb00034-0520-a.jpg

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