GATA4 mediates gene repression in the mature mouse small intestine through interactions with friend of GATA (FOG) cofactors

被引:37
作者
Beuling, Eva [2 ]
Bosse, Tjalling [2 ,3 ]
aan de Kerk, Daniel J. [3 ]
Piaseckyj, Christina M. [1 ]
Fujiwara, Yuko [4 ,5 ,6 ]
Katz, Samuel G. [4 ,5 ,6 ]
Orkin, Stuart H. [4 ,5 ,6 ]
Grand, Richard J. [1 ]
Krasinski, Stephen D. [1 ,7 ]
机构
[1] Childrens Hosp, Div Gastroenterol & Nutr, Dept Med, Boston, MA 02115 USA
[2] Erasmus Univ, Sch Med, NL-3000 DR Rotterdam, Netherlands
[3] Univ Amsterdam, Sch Med, NL-1100 DD Amsterdam, Netherlands
[4] Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Dana Farber Canc Inst, Dept Pediat, Boston, MA 02115 USA
[6] Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[7] Tufts Univ, Gerald J & Dorothy R Friedman Sch Nutr Sci & Poli, Boston, MA 02111 USA
关键词
GATA4; friend of GATA; FOG; intestinal differentiation; apical sodium-dependent; bile acid transporter; ASBT;
D O I
10.1016/j.ydbio.2008.07.022
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
GATA4, a transcription factor expressed in the proximal small intestine but not in the distal ileum, maintains proximal-distal distinctions by multiple processes involving gene repression, gene activation, and cell fate determination. Friend of GATA (FOG) is an evolutionarily conserved family of cofactors whose members physically associate with GATA factors and mediate GATA-regulated repression in multiple tissues. Using a novel, inducible, intestine-specific Gata4 knock-in model in mice, in which wild-type GATA4 is specifically inactivated in the small intestine, but a GATA4 mutant that does not bind FOG cofactors (GATA4ki) continues to be expressed, we found that ileal-specific genes were significantly induced in the proximal small intestine (P<0.01); in contrast, genes restricted to proximal small intestine and cell lineage markers were unaffected, indicating that GATA4-FOG interactions contribute specifically to the repression function of GATA4 within this organ. Fog1 mRNA displayed a proximal-distal pattern that parallels that of Gata4, and FOG1 protein was co-expressed with GATA4 in intestinal epithelia[ cells, implicating FOG] as the likely mediator of GATA4 function in the small intestine. Our data are the first to indicate FOG function and expression in the mammalian small intestine. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:179 / 189
页数:11
相关论文
共 51 条
[1]   Hepatocyte nuclear factor-1α is required for expression but dispensable for histone acetylation of the lactase-phlorizin hydrolase gene in vivo [J].
Bosse, T ;
van Wering, HM ;
Gielen, M ;
Dowling, LN ;
Fialkovich, JJ ;
Piaseckyj, CM ;
Gonzalez, FJ ;
Akiyama, TE ;
Montgomery, RK ;
Grand, RJ ;
Krasinski, SD .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2006, 290 (05) :G1016-G1024
[2]   Gata4 and Hnf1α are partially required for the expression of specific intestinal genes during development [J].
Bosse, Tjalling ;
Fialkovich, John J. ;
Piaseckyj, Christina M. ;
Beuling, Eva ;
Broekman, Henrike ;
Grand, Richard J. ;
Montgomery, Robert K. ;
Krasinski, Stephen D. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2007, 292 (05) :G1302-G1314
[3]   Gata4 is essential for the maintenance of Jejunal-Ileal identities in the adult mouse small intestine [J].
Bosse, Tjalling ;
Piaseckyj, Christina M. ;
Burghard, Ellen ;
Fialkovich, John J. ;
Rajagopal, Satish ;
Pu, William T. ;
Krasinski, Stephen D. .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (23) :9060-9070
[4]   Coregulation of GATA factors by the Friend of GATA (FOG) family of multitype zinc finger proteins [J].
Cantor, AB ;
Orkin, SH .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (01) :117-128
[5]   Distinct domains of the GATA-1 cofactor FOG-1 differentially influence erythroid versus megakaryocytic maturation [J].
Cantor, AB ;
Katz, SG ;
Orkin, SH .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (12) :4268-4279
[6]   GATA-factor dependence of the multitype zinc-finger protein FOG-1 for its essential role in megakaryopoiesis [J].
Chang, AN ;
Cantor, AB ;
Fujiwara, Y ;
Lodish, MB ;
Droho, S ;
Crispino, JD ;
Orkin, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (14) :9237-9242
[7]   The role of AP-1 in the transcriptional regulation of the rat apical sodium-dependent bile acid transporter [J].
Chen, F ;
Ma, L ;
Al-Ansari, N ;
Shneider, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (42) :38703-38714
[8]   Liver receptor homologue-1 mediates species- and cell line-specific bile acid-dependent negative feedback regulation of the apical sodium-dependent bile acid transporter [J].
Chen, F ;
Ma, L ;
Dawson, PA ;
Sinal, CJ ;
Sehayek, E ;
Gonzalez, FJ ;
Breslow, J ;
Ananthanarayanan, M ;
Shneider, BL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) :19909-19916
[9]   Use of altered specificity mutants to probe a specific protein-protein interaction in differentiation:: The GATA-1:FOG complex [J].
Crispino, JD ;
Lodish, MB ;
MacKay, JP ;
Orkin, SH .
MOLECULAR CELL, 1999, 3 (02) :219-228
[10]   Proper coronary vascular development and heart morphogenesis depend on interaction of GATA-4 with FOG cofactors [J].
Crispino, JD ;
Lodish, MB ;
Thurberg, BL ;
Litovsky, SH ;
Collins, T ;
Molkentin, JD ;
Orkin, SH .
GENES & DEVELOPMENT, 2001, 15 (07) :839-844