The Sox17-mCherry fusion mouse line allows visualization of endoderm and vascular endothelial development

被引:30
作者
Burtscher, Ingo [1 ]
Barkey, Wenke [1 ]
Schwarzfischer, Michael [2 ]
Theis, Fabian J. [2 ]
Lickert, Heiko [1 ]
机构
[1] Inst Stem Cell Res, Helmholtz Zentrum Munchen, Inst Diabet & Regenerat, D-85764 Neuherberg, Germany
[2] Helmholtz Zentrum Munchen, Inst Bioinformat & Syst Biol, D-85764 Neuherberg, Germany
关键词
Sox17; Foxa2; ES cells; mouse embryos; mCherry fluorescent reporter; endoderm; vasculature; live imaging; gastrulation; pancreas; lung; gut; DIFFERENTIAL EXPRESSION; GENE-EXPRESSION; REDUNDANT ROLES; CRE RECOMBINASE; SOX17; HNF-3-BETA; ASYMMETRY; PATTERN;
D O I
10.1002/dvg.20829
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sox17 is a HMG-box transcription factor that has been shown to play important roles in both cardio-vascular development and endoderm formation. To analyze these processes in greater detail, we have generated a Sox17-mCherry fusion (SCF) protein by gene targeting in ES cells. SCF reporter mice are homozygous viable and faithfully reflect the endogenous Sox17 protein localization. We report that SCF positive cells constitute a subpopulation in the visceral endoderm before gastrulation and time-lapse imaging reveals that SCF monitors the nascent definitive endoderm during epithelialization. After gastrulation, SCF marks the mid- and hindgut endoderm and vascular endothelial network, which can be imaged during establishment in allantois explant cultures. The SCF reporter is downregulated in the endoderm epithelium and upregulated in endothelial cells of the intestine, lung, and pancreas during organogenesis. In summary, the generation of the Sox17-mCherry reporter mouse line allows direct visualization of endoderm and vascular development in culture and the mouse embryo. genesis 50:496505, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:496 / 505
页数:10
相关论文
共 30 条
[21]   Gene expression pattern and progression of embryogenesis in the immediate post-implantation period of mouse development [J].
Pfister, Sabine ;
Steiner, Kirsten A. ;
Tam, Patrick P. L. .
GENE EXPRESSION PATTERNS, 2007, 7 (05) :558-573
[22]   Redundant roles of Sox17 and Sox18 in early cardiovascular development of mouse embryos [J].
Sakamoto, Youhei ;
Hara, Kenshiro ;
Kanai-Azuma, Masami ;
Matsui, Toshiyasu ;
Miura, Yutaroh ;
Tsunekawa, Naoki ;
Kurohmaru, Masamichi ;
Saijoh, Yukio ;
Koopman, Peter ;
Kanai, Yoshiakira .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 360 (03) :539-544
[23]  
SASAKI H, 1993, DEVELOPMENT, V118, P47
[24]   Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp red fluorescent protein [J].
Shaner, NC ;
Campbell, RE ;
Steinbach, PA ;
Giepmans, BNG ;
Palmer, AE ;
Tsien, RY .
NATURE BIOTECHNOLOGY, 2004, 22 (12) :1567-1572
[25]   Generalized lacZ expression with the ROSA26 Cre reporter strain [J].
Soriano, P .
NATURE GENETICS, 1999, 21 (01) :70-71
[26]   The anterior visceral endoderm-turning heads [J].
Srinivas, Shankar .
GENESIS, 2006, 44 (11) :565-572
[27]   SoxD proteins influence multiple stages of oligodendrocyte development and modulate SoxE protein function [J].
Stolt, C. Claus ;
Schlierf, Anita ;
Lommes, Petra ;
Hillgaertner, Simone ;
Werner, Torsten ;
Kosian, Thomas ;
Sock, Elisabeth ;
Kessaris, Nicoletta ;
Richardson, William D. ;
Lefebvre, Veronique ;
Wegner, Michael .
DEVELOPMENTAL CELL, 2006, 11 (05) :697-709
[28]   Building the mouse gastrula: signals, asymmetry and lineages [J].
Tam, Patrick P. L. ;
Loebel, David A. F. ;
Tanaka, Satomi S. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2006, 16 (04) :419-425
[29]   Nodal Dependent Differential Localisation of Dishevelled-2 Demarcates Regions of Differing Cell Behaviour in the Visceral Endoderm [J].
Trichas, Georgios ;
Joyce, Bradley ;
Crompton, Lucy A. ;
Wilkins, Vivienne ;
Clements, Melanie ;
Tada, Masazumi ;
Rodriguez, Tristan A. ;
Srinivas, Shankar .
PLOS BIOLOGY, 2011, 9 (02)
[30]   THE WINGED-HELIX TRANSCRIPTION FACTOR HNF-3-BETA IS REQUIRED FOR NOTOCHORD DEVELOPMENT IN THE MOUSE EMBRYO [J].
WEINSTEIN, DC ;
ALTABA, ARI ;
CHEN, WS ;
HOODLESS, P ;
PREZIOSO, VR ;
JESSELL, TM ;
DARNELL, JE .
CELL, 1994, 78 (04) :575-588