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c-Myc与Max结合至c-myc启动子的分析:通过间接机制发生自动抑制的证据。

Analysis of c-Myc and Max binding to the c-myc promoter: evidence that autosuppression occurs via an indirect mechanism.

作者信息

Buckle R S, Méchali M

机构信息

Institut Jacques Monod, Molecular Embryology Unit, Paris, France.

出版信息

Oncogene. 1995 Mar 16;10(6):1249-55.

PMID:7700652
Abstract

c-myc negatively autoregulates its expression at the level of transcriptional initiation, although the precise mechanism remains debated. While conclusive evidence for c-Myc binding in its own promoter has not been found, it has been proposed that c-Myc binds to a site upstream of the human c-myc gene which may also be a component of a replication origin (Ariga et al., 1989). In an attempt to clarify this issue, sequences flanking the c-myc gene were screened for c-Myc or Max binding sites using a novel procedure to facilitate the detection of DNA binding dependent upon long distance interactions or DNA secondary structure. Since the sequence specificity of DNA binding proteins may also be mediated by interaction with other proteins or by protein modification, this affinity capture assay was used in conjunction with nuclear extracts, potentially allowing the selection of novel in vivo DNA binding specificities. Using conditions that gave strong binding to an internal control sequence, c-Myc or Max binding elements were not detected in genomic sequences extending 5.4 kb upstream of the Xenopus c-myc gene. Identical results were obtained using both purified proteins and a variety of nuclear extracts, suggesting c-myc autosuppression most likely involves an indirect pathway.

摘要

c-myc在转录起始水平对其表达进行负向自调控,尽管确切机制仍存在争议。虽然尚未发现c-Myc在其自身启动子中结合的确凿证据,但有人提出c-Myc与人c-myc基因上游的一个位点结合,该位点也可能是复制起点的一个组成部分(有贺等人,1989年)。为了阐明这个问题,使用一种新方法筛选c-myc基因侧翼序列中的c-Myc或Max结合位点,以促进对依赖长距离相互作用或DNA二级结构的DNA结合的检测。由于DNA结合蛋白的序列特异性也可能通过与其他蛋白质的相互作用或蛋白质修饰来介导,因此这种亲和捕获测定法与核提取物一起使用,有可能筛选出新型的体内DNA结合特异性。在能与内部对照序列强烈结合的条件下,在非洲爪蟾c-myc基因上游延伸5.4 kb的基因组序列中未检测到c-Myc或Max结合元件。使用纯化蛋白和多种核提取物均得到相同结果,这表明c-myc的自抑制很可能涉及一条间接途径。

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