Opposing functions of the Ets factors NERF and ELF-1 during chicken blood vessel development

被引:15
作者
Gaspar, J
Thai, S
Voland, C
Dube, A
Libermann, TA
Iruela-Arispe, ML
Oettgen, P
机构
[1] Beth Israel Deaconess Med Ctr, New England Baptist Bone & Joint Inst, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Div Cardiol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA USA
关键词
angiogenesis; vasculogenesis; transcription; vascular biology; endothelium;
D O I
10.1161/01.ATV.0000023427.92642.CD
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective-The purpose of this study was to evaluate the role of the Ets factor NERF in the regulation of the Tie1 and Tie2 genes during chicken blood vessel development. Methods and Results-We have isolated the full-length cDNA for the chicken homologue of the human Ets factor NERF2 (cNERF2). Northern blot analysis and in situ hybridization demonstrate that cNERF2 is enriched in the developing blood vessels of the chicken chorioallantoic membrane. Interestingly, cNERF2 functions as a competitive inhibitor of a highly related Ets factor cELF-1 which we have previously shown to be enriched in chicken blood vessel development. Although in vitro-translated cELF-1 and cNERF2 can bind equally well to conserved Ets binding sites in the promoters of the Tie1 and Tie2 genes, cELF-1 preferentially binds to the Ets sites in these promoters during early stages of chicken blood vessel development, suggesting that cNERF may bind during later stages of blood vessel development and vascular remodeling. Conclusions-cNERF2 is enriched during embryonic and extraembryonic blood vessel development in the chicken and facilitates tight control of Tie1 and Tie2 gene regulation.
引用
收藏
页码:1106 / 1112
页数:7
相关论文
共 28 条
[1]
SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[2]
Role of the Ets transcription factors in the regulation of the vascular-specific Tie2 gene [J].
Dube, A ;
Akbarali, Y ;
Sato, TN ;
Libermann, TA ;
Oettgen, P .
CIRCULATION RESEARCH, 1999, 84 (10) :1177-1185
[3]
Dube A, 2001, CIRC RES, V88, P237
[4]
A PITFALL OF USING A 2ND PLASMID TO DETERMINE TRANSFECTION EFFICIENCY [J].
FARR, A ;
ROMAN, A .
NUCLEIC ACIDS RESEARCH, 1992, 20 (04) :920-920
[5]
TEL, a putative tumor suppressor, modulates cell growth and cell morphology of Ras-transformed cells while repressing the transcription of stromelysin-1 [J].
Fenrick, R ;
Wang, LL ;
Nip, J ;
Amann, JM ;
Rooney, RJ ;
Walker-Daniels, J ;
Crawford, HC ;
Hulboy, DL ;
Kinch, MS ;
Matrisian, LM ;
Hiebert, SW .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (16) :5828-5839
[6]
A SERIES OF NORMAL STAGES IN THE DEVELOPMENT OF THE CHICK EMBRYO [J].
HAMBURGER, V ;
HAMILTON, HL .
JOURNAL OF MORPHOLOGY, 1951, 88 (01) :49-&
[7]
HATVA E, 1995, AM J PATHOL, V146, P368
[8]
Role of Ets factors in the activity and endothelial cell specificity of the mouse Tie gene promoter [J].
Iljin, K ;
Dube, A ;
Kontusaari, S ;
Korhonen, J ;
Lahtinen, I ;
Oettgen, P ;
Alitalo, K .
FASEB JOURNAL, 1999, 13 (02) :377-386
[9]
KAIPAINEN A, 1994, CANCER RES, V54, P6571
[10]
Kappel A, 2000, BLOOD, V96, P3078