生物
分子生物学
转染
基因
报告基因
基因表达
互补DNA
胚胎干细胞
调节顺序
转基因
转录因子
基因表达调控
嵌合基因
细胞培养
遗传学
作者
Nissim Benvenisty,A Leder,Annie F. Kuo,Philip Leder
出处
期刊:Genes & Development
[Cold Spring Harbor Laboratory Press]
日期:1992-12-01
卷期号:6 (12b): 2513-2523
被引量:147
标识
DOI:10.1101/gad.6.12b.2513
摘要
We have used a subtraction/coexpression strategy involving two different tumors derived from c-myc-bearing transgenic mice to identify a gene that is a target for c-Myc regulation. The gene, expressed in certain embryonic and adult tissues and in several (but not all) c-myc-based tumors, bears a functional c-Myc-binding sequence located 3' to its transcription start site. This sequence is required for the binding of a nuclear protein complex which, by antibody analysis, includes c-Myc. This site is also required for expression of a reporter gene in chimeric constructs transfected into c-myc-overexpressing cells and, conversely, requires c-myc cotransfection for its enhanced expression in COS cells. Furthermore, transfection of c-myc blocks the normal down-regulation of this gene, which occurs in embryonic stem cells as they undergo differentiation. This target gene encodes an anonymous cDNA (ECA39) found previously to be amplified in a teratocarcinoma cell line.
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