tom-1, a novel v-Myb target gene expressed in AMV- and E26-transformed myelomonocytic cells

被引:58
作者
Burk, O
Worpenberg, S
Haenig, B
Klempnauer, KH
机构
[1] MAX PLANCK INST IMMUNBIOL,HANS SPEMANN LAB,D-79108 FREIBURG,GERMANY
[2] UNIV FREIBURG,KINDERKLIN,D-79106 FREIBURG,GERMANY
关键词
C/EBP; myelomonocytic cells; target gene; tom-1; gene; v-myb oncogene;
D O I
10.1093/emboj/16.6.1371
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The retroviral oncogene v-myb is a mutated and truncated version of the c-myb proto-oncogene and encodes a transcription factor (v-Myb) that specifically transforms myelomonocytic cells, Two different variants of v-myb, transduced independently by the oncogenic chicken retroviruses AMV and E26, have been characterized, It is believed that both variants of v-Myb transform myelomonocytic cells by affecting the expression of specific genes; however, no target genes common to both oncogenic viruses have been identified, Here, we describe the identification of a novel v-Myb target gene, designated as tom-1 (target of myb 1), The tom-1 gene has two promoters, one of which is Myb-inducible, tom-1 is expressed at elevated levels in AMV-transformed as well as in E26-transformed myeloid cells, We show that tom-1 activation by v-Myb does not require de novo protein synthesis and that the Myb-inducible tom-1 promoter contains a functional Myb binding site, Thus, tom-1 is the first example of a direct target gene for both oncogenic forms of the v-myb gene, Further analysis of the Myb-inducible tom-1 promoter shows that a C/EBP binding site is juxtaposed to the Myb binding site and that C/EBP is required for the Myb-dependent activation of the promoter, Together with previous work our results suggest that C/EBP may be a general cooperation partner for v-Myb in myelomonocytic cells.
引用
收藏
页码:1371 / 1380
页数:10
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