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c-myb和B-myb基因产物对c-myc基因的转录激活作用。

Transcriptional activation of the c-myc gene by the c-myb and B-myb gene products.

作者信息

Nakagoshi H, Kanei-Ishii C, Sawazaki T, Mizuguchi G, Ishii S

机构信息

Laboratory of Molecular Genetics, Tsukuba Life Science Center, Institute of Physical and Chemical Research (RIKEN), Ibaraki, Japan.

出版信息

Oncogene. 1992 Jun;7(6):1233-40.

PMID:1594249
Abstract

To identify the target genes modulated by the myb gene product (Myb), a co-transfection assay with a Myb expression plasmid was performed. Both c-Myb and B-Myb, another member of the myb gene family, trans-activated the human c-myc promoter. DNAase I footprint analysis using the bacterially expressed c-Myb, identified multiple c-Myb binding sites in the c-myc promoter region. Deletion analysis of the c-myc promoter suggested that some number of Myb binding sites, not a specific Myb binding site, is important for the c-Myb-induced trans-activation of the c-myc promoter. Using the c-myc-chloramphenicol acetyltransferase (CAT) construct as a reporter in a co-transfection assay, the domains of c-Myb required for trans-activation were examined. The functional domains of c-Myb identified using the c-myc promoter were almost the same as those identified previously with the artificial target gene containing Myb binding sites, but unlike the case with the artificial target gene the N-terminal half of the previously identified negative regulatory domains and the C-terminal 136 amino acids were required for the maximal trans-activation of the c-myc promoter. These results indicate that there are some differences in the regulation of Myb-dependent trans-activation in different target genes.

摘要

为了鉴定由myb基因产物(Myb)调控的靶基因,进行了Myb表达质粒的共转染实验。c-Myb和myb基因家族的另一个成员B-Myb均能反式激活人c-myc启动子。使用细菌表达的c-Myb进行DNA酶I足迹分析,在c-myc启动子区域鉴定出多个c-Myb结合位点。c-myc启动子的缺失分析表明,一定数量的Myb结合位点而非特定的Myb结合位点对c-Myb诱导的c-myc启动子反式激活很重要。在共转染实验中使用c-myc-氯霉素乙酰转移酶(CAT)构建体作为报告基因,检测了反式激活所需的c-Myb结构域。使用c-myc启动子鉴定的c-Myb功能结构域与先前使用含Myb结合位点的人工靶基因鉴定的结构域几乎相同,但与人工靶基因的情况不同,先前鉴定的负调控结构域的N端一半和C端136个氨基酸是c-myc启动子最大反式激活所必需的。这些结果表明,Myb依赖性反式激活在不同靶基因中的调控存在一些差异。

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