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与tRNA基因内部启动子元件结合的锥虫核因子。

Trypanosome nuclear factors which bind to internal promoter elements of tRNA genes.

作者信息

Bell S D, Barry J D

机构信息

Wellcome Unit of Molecular Parasitology, Anderson College, Glasgow, UK.

出版信息

Nucleic Acids Res. 1995 Aug 25;23(16):3103-10. doi: 10.1093/nar/23.16.3103.

Abstract

Expression of eukaryotic nuclear encoded tRNA genes requires two transcription factors, TFIIIB and TFIIIC. To determine if the highly evolutionarily diverged parasitic protozoan Trypanosoma brucei possesses any analogous factors, trypanosome nuclear extracts were prepared. Using these extracts in gel-retardation assays on trypanosome tRNA genes we detected three specific protein-DNA complexes, a highly retarded species and a less retarded pair of complexes. Introduction of mutations into the B box of a lysyl tRNA gene greatly reduced formation of all three complexes. Footprinting studies indicated that all complexes protected the B box of the tRNA gene from cleavage. The most highly retarded complex protected both the A and B boxes from DNasel cleavage. The less retarded pair of complexes showed footprints on the B box alone and the lowest B box specific complex is shown to be resistant to the polyanion heparin. All three complexes are demonstrated to induce bends in the DNA on binding.

摘要

真核细胞核编码的tRNA基因的表达需要两种转录因子,即TFIIIB和TFIIIC。为了确定高度进化分化的寄生原生动物布氏锥虫是否拥有任何类似的因子,制备了锥虫核提取物。利用这些提取物对锥虫tRNA基因进行凝胶阻滞分析,我们检测到三种特异性的蛋白质-DNA复合物,一种高度阻滞的复合物和一对阻滞程度较轻的复合物。将赖氨酸tRNA基因的B框引入突变,大大减少了所有三种复合物的形成。足迹研究表明,所有复合物都能保护tRNA基因的B框不被切割。高度阻滞的复合物保护A框和B框不被DNA酶I切割。阻滞程度较轻的一对复合物仅在B框上显示足迹,而最低的B框特异性复合物对多阴离子肝素具有抗性。所有三种复合物在结合时都能诱导DNA弯曲。

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