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The 3' flanking region of the human ABO histo-blood group gene is involved in negative regulation of gene expression.

机译:人类ABO组织血型基因的3'侧翼区域参与基因表达的负调控。

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摘要

Gene expression is driven by promoters, enhancers, silencers, and other cis-regulatory elements upstream and downstream of the gene. Previous studies of the regulation of human ABO gene transcription have focused mainly on the 5' region, including the core promoter and the region proximal to it. However, as the involvement of the 3' flanking region in transcriptional regulation has not yet been examined, we focused on this issue. The 3' region approximately 2.2kb downstream of the ABO gene was PCR-amplified and inserted into a cloning vector, followed by sequence determination and preparation of luciferase reporter vectors. Transient transfections into KATOIII and K562 cells were performed using various reporter plasmids containing the 3' region. The 3' region of the ABO gene, which was characterized by a high degree of sequence repetition, was effectively cloned by a single-copy cloning method. Transfections in KATOIII and K562 cells showed that negative elements were demonstrable within the 3' region. These observations suggest that negative regulatory elements seem to be present in the 3' region of ABO in both epithelial and erythroid lineages. As we had observed a negative region just upstream of the ABO promoter, transcription from ABO could be negatively regulated by repressive regions just upstream of the promoter and downstream of the gene. Further studies of the enhancer will be required for elucidating the molecular basis of ABO gene expression.
机译:基因表达由基因上游和下游的启动子,增强子,沉默子和其他顺式调控元件驱动。先前关于人类ABO基因转录调控的研究主要集中在5'区域,包括核心启动子及其附近区域。但是,由于尚未研究3'侧翼区域在转录调控中的参与,因此我们将重点放在此问题上。 PCR扩增ABO基因下游约2.2kb的3'区域,并将其插入克隆载体中,随后进行序列测定和荧光素酶报道载体的制备。使用含有3'区的各种报告质粒,瞬时转染到KATOIII和K562细胞中。通过单拷贝克隆方法有效克隆了以高度重复序列为特征的ABO基因的3'区。 KATOIII和K562细胞的转染表明,在3'区域内可证实存在负性元件。这些观察表明,在上皮和红系谱系的ABO的3'区域中似乎存在负调控元件。因为我们已经观察到ABO启动子上游的负区,所以ABO的转录可能受到启动子上游和基因下游的阻抑区的负调控。为了阐明ABO基因表达的分子基础,将需要对增强子进行进一步的研究。

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