AN EMBRYONICALLY EXPRESSED GENE IS A TARGET FOR C-MYC REGULATION VIA THE C-MYC-BINDING SEQUENCE

被引:156
作者
BENVENISTY, N
LEDER, A
KUO, A
LEDER, P
机构
[1] Department of Genetics, Harvard Medical School, Howard Hughes Medical Institute, Boston
关键词
C-MYC; DNA-BINDING; TRANSFORMATION; TRANSGENIC MICE; EMBRYO;
D O I
10.1101/gad.6.12b.2513
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
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.
引用
收藏
页码:2513 / 2523
页数:11
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