Combinatorial function of ETS transcription factors in the developing vasculature

被引:162
作者
Pham, Van N.
Lawson, Nathan D.
Mugford, Joshua W.
Dye, Louis
Castranova, Daniel
Lo, Brigid
Weinstein, Brant M.
机构
[1] NICHD, Mol Genet Lab, NIH, Bethesda, MD 20892 USA
[2] NICHD, Microscopy & Imaging Core, NIH, Bethesda, MD USA
关键词
zebrafish; ETS transcription factors; intersegmental vessels; vascular development; angiogenesis;
D O I
10.1016/j.ydbio.2006.10.030
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Members of the ETS family of transcription factors are among the first genes expressed in the developing vasculature, but loss-of-function experiments for individual ETS factors in mice have not uncovered important early functional roles for these genes. However, multiple ETS factors are expressed in spatially and temporally overlapping patterns in the developing vasculature, suggesting possible functional overlap. We have taken a comprehensive approach to exploring the function of these factors during vascular development by employing the genetic and experimental tools available in the zebrafish to analyze four ETS family members expressed together in the zebrafish vasculature; fli1, fli1b, ets1, and etsrp. We isolated and characterized an ENU-induced mutant with defects in trunk angiogenesis and positionally cloned the defective gene from this mutant, etsrp. Using the etsrp morpholinos targeting each of the four genes, we show that the four ETS factors function combinatorially during vascular and hematopoietic development. Reduction of etsrp or any of the other genes alone results in either partial or no defects in endothelial differentiation, while combined reduction in the function of all four genes causes dramatic loss of endothelial cells. Our results demonstrate that combinatorial ETS factor function is essential for early endothelial specification and differentiation. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:772 / 783
页数:12
相关论文
共 45 条
[1]  
Baltzinger M, 1999, DEV DYNAM, V216, P420, DOI 10.1002/(SICI)1097-0177(199912)216:4/5<420::AID-DVDY10>3.0.CO
[2]  
2-C
[3]   Mouse models in the study of the Ets family of transcription factors [J].
Bartel, FO ;
Higuchi, T ;
Spyropoulos, DD .
ONCOGENE, 2000, 19 (55) :6443-6454
[4]   The Ets-1 transcription factor is required for the development of natural killer cells in mice [J].
Barton, K ;
Muthusamy, N ;
Fischer, C ;
Ting, CN ;
Walunas, TL ;
Lanier, LL ;
Leiden, JM .
IMMUNITY, 1998, 9 (04) :555-563
[5]   INCREASED T-CELL APOPTOSIS AND TERMINAL B-CELL DIFFERENTIATION-INDUCED BY INACTIVATION OF THE ETS-1 PROTOONCOGENE [J].
BORIES, JC ;
WILLERFORD, DM ;
GREVIN, D ;
DAVIDSON, L ;
CAMUS, A ;
MARTIN, P ;
STEHELIN, D ;
ALT, FW .
NATURE, 1995, 377 (6550) :635-638
[6]   Insights into early vasculogenesis revealed by expression of the ETS-domain transcription factor Fli-1 in wild-type and mutant zebrafish embryos [J].
Brown, LA ;
Rodaway, ARF ;
Schilling, TF ;
Jowett, T ;
Ingham, PW ;
Patient, RK ;
Sharrocks, AD .
MECHANISMS OF DEVELOPMENT, 2000, 90 (02) :237-252
[7]   INTRAEMBRYONIC HEMATOPOIETIC-CELL MIGRATION DURING VERTEBRATE DEVELOPMENT [J].
DETRICH, HW ;
KIERAN, MW ;
CHAN, FY ;
BARONE, LM ;
YEE, K ;
RUNDSTADLER, JA ;
PRATT, S ;
RANSOM, D ;
ZON, LI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10713-10717
[8]   Vessel patterning in the embryo of the zebrafish: Guidance by notochord [J].
Fouquet, B ;
Weinstein, BM ;
Serluca, FC ;
Fishman, MC .
DEVELOPMENTAL BIOLOGY, 1997, 183 (01) :37-48
[9]   Loss of Gata1 but not Gata2 converts erythropoiesis to myelopoiesis in zebrafish embryos [J].
Galloway, JL ;
Wingert, RA ;
Thisse, C ;
Thisse, B ;
Zon, LI .
DEVELOPMENTAL CELL, 2005, 8 (01) :109-116
[10]   Fli-1 is required for murine vascular and megakaryocytic development and is hemizygously deleted in patients with thrombocytopenia [J].
Hart, A ;
Melet, F ;
Grossfeld, P ;
Chien, K ;
Jones, C ;
Tunnacliffe, A ;
Favier, R ;
Bernstein, A .
IMMUNITY, 2000, 13 (02) :167-177