ERF: Genomic organization, chromosomal localization and promoter analysis of the human and mouse genes

被引:17
作者
Liu, DR
Pavlopoulos, E
Modi, W
Moschonas, N
Mavrothalassitis, G
机构
[1] NCI,FREDERICK CANC RES & DEV CTR,MOL ONCOL LAB,FREDERICK,MD 21702
[2] NCI,FREDERICK CANC RES & DEV CTR,SAIC,FREDERICK,MD 21702
[3] FORTH,INST MOL BIOL & BIOTECHNOL,IRAKLION 71110,GREECE
[4] UNIV CRETE,DEPT BIOL,IRAKLION 71110,GREECE
关键词
ets; transcriptional repressor; genomic organization; promoter;
D O I
10.1038/sj.onc.1200965
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
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 ERI; 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 ERP 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.
引用
收藏
页码:1445 / 1451
页数:7
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