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小鼠5S核糖体RNA基因的特征分析

Characterization of 5S rRNA genes from mouse.

作者信息

Hallenberg C, Nederby Nielsen J, Frederiksen S

机构信息

Department of Medical Biochemistry and Genetics, Panum Institute, University of Copenhagen, Denmark.

出版信息

Gene. 1994 May 16;142(2):291-5. doi: 10.1016/0378-1119(94)90277-1.

Abstract

In order to characterize the transcriptional regulation of the 5S rRNA genes we have isolated a bona fide gene and a pseudogene from mouse cells. These 5S rRNA genes contain a 12-bp sequence designated as the D-box, located in position -33 to -22 bp, and two Sp1-binding sites in the 5'-flanking region. The D-box is conserved in human and hamster 5S rRNA genes although in slightly different upstream positions. The bona fide mouse 5S rRNA gene was transcribed in a HeLa S-100 extract. The transcriptional activity of this gene was only 50% of that of the human gene, indicating the involvement of species-specific transcription factors and/or polymerases. The pseudogene which contains the D-box, but with position +25 to +35 bp deleted, showed no transcriptional activity. Deletion of the D-box in the 5'-flanking sequence abolished transcriptional activity, indicating that this conserved sequence is of importance for gene expression.

摘要

为了表征5S rRNA基因的转录调控,我们从小鼠细胞中分离出了一个真正的基因和一个假基因。这些5S rRNA基因包含一个位于-33至-22 bp位置的12 bp序列,称为D框,以及5'侧翼区域中的两个Sp1结合位点。D框在人类和仓鼠5S rRNA基因中是保守的,尽管其上游位置略有不同。真正的小鼠5S rRNA基因在HeLa S-100提取物中被转录。该基因的转录活性仅为人基因的50%,表明存在物种特异性转录因子和/或聚合酶。假基因包含D框,但缺失了+25至+35 bp的位置,没有显示出转录活性。5'侧翼序列中D框的缺失消除了转录活性,表明这个保守序列对基因表达很重要。

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