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A common feature shared by bent DNA structures locating in the eukaryotic promoter region.

机译:位于真核启动子区域的弯曲DNA结构共有一个共同特征。

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Eukaryotic promoters often contain a bent DNA structure, suggesting that this structure plays some role in transcription. To reveal the role, we need more information on the promoters that contain or flank a bent DNA structure. In this study, we collected such promoters by the following approach: we first isolated human genomic DNA fragments that contained at least one bent DNA structure, then shotgun cloned them into a promoter trap vector, screened DNA fragments that functioned as a promoter, and finally found the promoters of interest by determining the bent DNA locus and the region expressing promoter activity. From 1,187 recombinant plasmids, we isolated 51 that showed promoter activity. Structural and functional analyses of randomly selected 10 clones with inserts of 548-913 bp demonstrated 11 sequences that could drive transcription. Unexpectedly, all of these clones met our purpose: i.e., each segment that showed a promoter activity (67-179 bp) was very close to the bent DNA structure (spanning about 150 bp in all clones), and in some cases overlapped it. More interestingly, these bent DNA structures all had a superhelical writhe. We propose a hypothesis that in the bent-DNA-containing eukaryotic promoters. bent DNA organizes local chromatin infrastructure appropriately for transcription initiation.
机译:真核启动子通常包含弯曲的DNA结构,表明该结构在转录中起一定作用。要揭示其作用,我们需要有关包含或位于弯曲DNA结构侧面的启动子的更多信息。在这项研究中,我们通过以下方法收集了此类启动子:我们首先分离了包含至少一个弯曲DNA结构的人类基因组DNA片段,然后将散弹枪将其克隆到启动子捕获载体中,筛选出具有启动子功能的DNA片段,最后通过确定弯曲的DNA基因座和表达启动子活性的区域,发现了感兴趣的启动子。从1,187个重组质粒中,我们分离出51个具有启动子活性的质粒。随机选择的10个具有548-913 bp插入片段的克隆的结构和功能分析表明,有11个序列可以驱动转录。出乎意料的是,所有这些克隆都达到了我们的目的:即,显示启动子活性的每个片段(67-179 bp)都非常接近弯曲的DNA结构(在所有克隆中跨越约150 bp),在某些情况下重叠了该片段。更有趣的是,这些弯曲的DNA结构都具有超螺旋扭曲。我们提出了一个假说,即在含有弯曲DNA的真核启动子中。弯曲的DNA适当地组织了局部染色质基础结构以进行转录起始。

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