Foxp4:: a novel member of the Foxp subfamily of winged-helix genes co-expressed with Foxp1 and Foxp2 in pulmonary and gut tissues

被引:66
作者
Lu, Min Min
Li, Shanru
Yang, Honghua
Morrisey, Edward E. [1 ]
机构
[1] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[3] Univ Penn, Mol Cardiol Res Ctr, Philadelphia, PA 19104 USA
关键词
Foxp1; Foxp2; Foxp4; winged-helix; transcriptional repression; lung epithelium; intestinal epithelium;
D O I
10.1016/S0925-4773(03)00116-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study, we describe the isolation and characterization of Foxp4, a new member of the Foxp subfamily of winged-helix transcription factors. The full-length mouse Foxp4 cDNA encodes a 685-amino-acid protein that is similar to Foxp1 and Foxp2. Foxp4 gene expression is observed primarily in pulmonary, neural, and gut tissues during embryonic development. To compare the protein expression patterns of Foxp4 to Foxp1 and Foxp2, specific polyclonal antisera to each of these proteins was used in immunohistochemical analysis of mouse embryonic tissues. All three proteins are expressed in lung epithelium with Foxp1 and Foxp4 expressed in both proximal and distal airway epithelium while Foxp2 is expressed primarily in distal epithelium. Foxp1 protein expression is also observed in the mesenchyme and vascular endothelial cells of the lung. At embryonic day 12.5, Foxp1 and Foxp2 are expressed in both the mucosal and epithelial layers of the intestine. However, Foxp2 is expressed only in the outer mucosal layer of the intestine and stomach later in development. Finally, Foxp4 is expressed exclusively in the epithelial cells of the developing intestine, where, in late development, it is expressed in a gradient along the longitudinal axis of the villi. (c) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:S197 / S202
页数:6
相关论文
共 19 条
[1]   HNF-3-BETA IS ESSENTIAL FOR NODE AND NOTOCHORD FORMATION IN MOUSE DEVELOPMENT [J].
ANG, SL ;
ROSSANT, J .
CELL, 1994, 78 (04) :561-574
[2]   Combinatorial action of HNF3 and Sp family transcription factors in the activation of the rabbit uteroglobin/CC10 promoter [J].
Braun, H ;
Suske, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (16) :9821-9828
[3]   HNF3β and GATA-4 transactivate the liver-enriched homeobox gene, Hex [J].
Denson, LA ;
McClure, MH ;
Bogue, CW ;
Karpen, SJ ;
Jacobs, HC .
GENE, 2000, 246 (1-2) :311-320
[4]   Human SP-C gene sequences that confer lung epithelium-specific expression in transgenic mice [J].
Glasser, SW ;
Burhans, MS ;
Eszterhas, SK ;
Bruno, MD ;
Korfhagen, TR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2000, 278 (05) :L933-L945
[5]   Xenopus brain factor-2 controls mesoderm, forebrain and neural crest development [J].
Gómez-Skarmeta, JL ;
de la Calle-Mustienes, E ;
Modolell, J ;
Mayor, R .
MECHANISMS OF DEVELOPMENT, 1999, 80 (01) :15-27
[6]  
Kaestner KH, 2000, GENE DEV, V14, P142
[7]   GATA4 transcription factor is required for ventral morphogenesis and heart tube formation [J].
Kuo, CT ;
Morrisey, EE ;
Anandappa, R ;
Sigrist, K ;
Lu, MM ;
Parmacek, MS ;
Soudais, C ;
Leiden, JM .
GENES & DEVELOPMENT, 1997, 11 (08) :1048-1060
[8]  
Labosky PA, 1997, DEVELOPMENT, V124, P1263
[9]   Transcriptional regulation of the surfactant protein-A gene in fetal lung [J].
Mendelson, CR ;
Gao, E ;
Young, PP ;
Michael, LF ;
Alcorn, JL .
CHEST, 1997, 111 (06) :S96-S104
[10]  
Morrison B, 1998, SWINE HEALTH PROD, V6, P4