Cooperative interactions among intestinal GATA factors in activating the rat liver fatty acid binding protein gene

被引:9
作者
Divine, Joyce K.
Staloch, Lora J.
Haveri, Hanna
Rowley, Christopher W.
Heikinheimo, Markku
Simon, Theodore C.
机构
[1] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Div Biol & Biomed Sci, St Louis, MO 63110 USA
[3] Univ Helsinki, Childrens Hosp, Helsinki, Finland
[4] Univ Helsinki, Program Dev & Reprod Biol, Helsinki, Finland
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2006年 / 291卷 / 02期
关键词
fabp1; GATA-4; GATA-5; GATA-6; suckling-weaning transition;
D O I
10.1152/ajpgi.00422.2003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Cooperative interactions among intestinal GATA factors in activating the rat liver fatty acid binding protein gene. Am J Physiol Gastrointest Liver Physiol 291: G297-G306, 2006. First published April 6, 2006; doi:10.1152/ajpgi.00422.2003. - GATA-4, GATA-5, and GATA-6 are endodermal zinc-finger transcription factors that activate numerous enterocytic genes. GATA-4 and GATA-6 but not GATA-5 are present in adult murine small intestinal enterocytes, and we now report the simultaneous presence of all three GATA factors in murine small intestinal enterocytes before weaning age. An immunohistochemical survey detected enterocytic GATA-4 and GATA-6 at birth and 1 wk of age and GATA-5 at 1 wk but not birth. Interactions among GATA factors were explored utilizing a transgene constructed from the proximal promoter of the rat liver fatty acid binding protein gene (Fabp1). GATA-4 and GATA-5 but not GATA-6 activate the Fabp1 transgene through a cognate binding site at -128. A dose-response assay revealed a maximum in transgene activation by both factors, where additional factor did not further increase transgene activity. However, at saturated levels of GATA-4, additional transgene activation was achieved by adding GATA-5 expression construct, and vice versa. Similar cooperativity occurred with GATA-5 and GATA-6. Identical interactions were observed with a target transgene consisting of a single GATA site upstream of a minimal promoter. Furthermore, GATA-4 and GATA-5 or GATA-5 and GATA-6 bound to each other in solution. These results are consistent with tethering of one GATA factor to the Fabp1 promoter through interaction with a second GATA factor to produce increased target gene activation. Cooperative target gene activation was specific to an intestinal cell line and may represent a mechanism by which genes are activated in the small intestinal epithelium during the period before weaning.
引用
收藏
页码:G297 / G306
页数:10
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