Liu D, Pavlopoulos E, Modi W, Moschonas N, Mavrothalassitis G
SAIC, National Cancer Institute-FCRDC, Frederick, Maryland 21702-1201, USA.
Oncogene. 1997 Mar 27;14(12):1445-51. doi: 10.1038/sj.onc.1200965.
ERF (Ets2 Repressor Factor) is a ubiquitously expressed ets-domain protein that exhibits strong transcriptional repressor activity, has been shown to suppress ets-induced transformation and has been suggested to be regulated by MAPK phosphorylation. We report here the sequence of the mouse gene, the genomic organization of the human and the mouse genes, their chromosomal position and the analysis of the promoter region. Genomic clones encompassing either the human ERF or the mouse Erf gene were isolated and utilized to define their molecular organization. The gene in both species consists of 4 exons over a 10 kb region. Utilizing FISH, somatic cell hybrids and linkage analysis, we identified the chromosomal position of ERF on human chromosome 19q13.1 and on its syntenic region in the mouse, on chromosome 7. Sequence analysis of the mouse gene indicated a 90% identity to the human gene within the coding and promoter regions. The predicted Erf protein is 98% identical to the human protein and all of the identifiable motifs are conserved between the two proteins. However, the mouse protein is three amino acids longer (551 versus 548 aa). The area surrounding the region that is homologous to the 5' end of the human cDNA can serve as a promoter in transfection into eukaryotic cells. This region is highly conserved between the mouse and the human genes. A number of conserved transcription factor binding sites can be identified in the region including an ets binding site (EBS). Interestingly, removal of a small segment that includes the EBS, seriously hampers promoter function, suggesting the ERF transcription may be regulated by ets-domain proteins.
ERF(Ets2 阻遏因子)是一种广泛表达的 Ets 结构域蛋白,具有强大的转录抑制活性,已被证明可抑制 Ets 诱导的细胞转化,并被认为受 MAPK 磷酸化调控。我们在此报告小鼠基因的序列、人类和小鼠基因的基因组结构、它们的染色体定位以及启动子区域的分析。分离出包含人类 ERF 或小鼠 Erf 基因的基因组克隆,并用于确定它们的分子结构。这两个物种的基因在 10 kb 区域内均由 4 个外显子组成。利用荧光原位杂交、体细胞杂种和连锁分析,我们确定了 ERF 在人类染色体 19q13.1 及其在小鼠中的同线性区域(染色体 7)上的染色体定位。小鼠基因的序列分析表明,在编码区和启动子区域与人类基因有 90%的同一性。预测的 Erf 蛋白与人类蛋白有 98%的同一性,并且两种蛋白之间所有可识别的基序都是保守的。然而,小鼠蛋白长三个氨基酸(551 个氨基酸对 548 个氨基酸)。与人类 cDNA 5'端同源区域周围的区域在转染到真核细胞中时可作为启动子。该区域在小鼠和人类基因之间高度保守。在该区域可鉴定出许多保守的转录因子结合位点,包括一个 Ets 结合位点(EBS)。有趣的是,去除包含 EBS 的一小段序列会严重阻碍启动子功能,这表明 ERF 转录可能受 Ets 结构域蛋白调控。