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免疫球蛋白重链微卫星对腺病毒主要晚期启动子的USF结合位点和Eμ介导的转录激活的抑制作用。

IGH minisatellite suppression of USF-binding-site- and E mu-mediated transcriptional activation of the adenovirus major late promoter.

作者信息

Trepicchio W L, Krontiris T G

机构信息

Department of Medicine (Hematology/Oncology), New England Medical Center Hospitals, Tufts University School of Medicine, Boston, MA 02111.

出版信息

Nucleic Acids Res. 1993 Feb 25;21(4):977-85. doi: 10.1093/nar/21.4.977.

Abstract

The 50bp repeat unit of the minisatellite within the DH-JH interval of the human immunoglobulin heavy chain locus binds a nuclear factor present in a wide variety of cell types. The binding site contains the myc/HLH motif, CACGTG, and represents a 15 of 17 base match for the USF/MLTF binding site adjacent to the adenovirus major late promoter (MLP). Unlike the USF/MLTF site, the IGH minisatellite possesses no enhancer activity. However, it can significantly suppress, in cis and in trans, USF-site-mediated transcriptional activation of the MLP. In murine myeloma cells, the IGH minisatellite can suppress, in trans, MLP activation by the murine heavy chain gene enhancer, E mu. These activities potentially represent a DNA-based form of squelching.

摘要

人类免疫球蛋白重链基因座DH-JH区间内小卫星的50bp重复单元可结合多种细胞类型中存在的一种核因子。该结合位点包含myc/HLH基序CACGTG,与腺病毒主要晚期启动子(MLP)相邻的USF/MLTF结合位点有17个碱基中的15个相匹配。与USF/MLTF位点不同,IGH小卫星不具有增强子活性。然而,它可以顺式和反式显著抑制USF位点介导的MLP转录激活。在鼠骨髓瘤细胞中,IGH小卫星可以反式抑制鼠重链基因增强子Eμ对MLP的激活。这些活性可能代表一种基于DNA的淬灭形式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2679/309232/fff06d0ada03/nar00053-0188-a.jpg

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