Petrenko O, Ischenko I, Enrietto P J
Department of Microbiology, State University of New York at Stony Brook, 11794, USA.
Oncogene. 1997 Oct 2;15(14):1671-80. doi: 10.1038/sj.onc.1201334.
In this study, alterations in gene expression patterns have been examined in v-Rel-transformed avian bone marrow cells. Using a conditional v-Rel estrogen receptor chimera (v-RelER) which transforms cells in an estrogen-dependent manner, we constructed subtraction cDNA libraries from v-RelER-transformed bone marrow cells. Several different sequences were identified whose expression was altered upon hormone activation of v-RelER. These include two genes related to the MIP-1 chemokine family (mip-1beta and a tca3 homologue), a cell surface antigen sca-2 and the transcription factor nfkb1. The expression of each gene was assayed in a number of wild-type and mutant v-Rel-expressing fibroblast and hematopoietic cells. All v-Rel-transformed hematopoietic cells tested express high levels of nfkb1 and sca-2. In fibroblasts, wild-type v-Rel induced expression of mip-1beta and nfkb1, while nontransforming mutants of v-Rel failed to do so, suggesting a role for these two genes in v-Rel mediated transformation. Finally, these genes are expressed at high levels in cells overexpressing wild-type and truncated forms of c-Rel, implying that v-Rel transforms, in part, by induction of c-Rel target genes.
在本研究中,已对v-Rel转化的禽类骨髓细胞中的基因表达模式改变进行了检测。使用一种以雌激素依赖方式转化细胞的条件性v-Rel雌激素受体嵌合体(v-RelER),我们从v-RelER转化的骨髓细胞构建了消减cDNA文库。鉴定出了几个不同的序列,其表达在v-RelER的激素激活后发生改变。这些包括两个与MIP-1趋化因子家族相关的基因(mip-1β和一个tca3同源物)、一种细胞表面抗原sca-2和转录因子nfkb1。在一些野生型和表达突变型v-Rel的成纤维细胞及造血细胞中检测了每个基因的表达。所有测试的v-Rel转化的造血细胞都高水平表达nfkb1和sca-2。在成纤维细胞中,野生型v-Rel诱导mip-1β和nfkb1的表达,而v-Rel的非转化突变体则不能,这表明这两个基因在v-Rel介导的转化中起作用。最后,这些基因在过表达野生型和截短形式c-Rel的细胞中高水平表达,这意味着v-Rel部分地通过诱导c-Rel靶基因来实现转化。