Functional conservation of interactions between a homeodomain cofactor and a mammalian FTZ-F1 homologue

被引:52
作者
Steffensen, KR
Holter, E
Båvner, A
Nilsson, M
Pelto-Huikko, M
Tomarev, S
Treuter, E [1 ]
机构
[1] Karolinska Inst, Novum, Dept Biosci, S-14157 Huddinge, Sweden
[2] Tampere Univ, Dept Dev Biol, Sch Med, FIN-33101 Tampere, Finland
[3] Tampere Univ Hosp, Dept Pathol, Tampere 33101, Finland
[4] NEI, Mol & Dev Biol Lab, NIH, Bethesda, MD 20892 USA
关键词
nuclear receptor; homeodomain; Prox1; FTZ-F1; LRH1;
D O I
10.1038/sj.embor.7400147
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear receptors are master regulators of metazoan gene expression with crucial roles during development and in adult physiology. Fushi tarazu factor 1 (FTZ-F1) subfamily members are ancient orphan receptors with homologues from Drosophila to human that regulate diverse gene expression programs important for developmental processes, reproduction and cholesterol homeostasis in an apparently ligand-independent manner. Thus, developmental and tissue-specific cofactors may be particularly important in modulating the transcriptional activities of FTZ-F1 receptors. In Drosophila, the homeodomain protein Fushi tarazu acts as a cofactor for FTZ-F1 (NR5A3), leading to the hypothesis that a similar type of homeodomain cofactor-nuclear receptor relationship might exist in vertebrates. In this study, we have identified and characterized the homeodomain protein Prox1 as a co-repressor for liver receptor homologue 1 (LRH1/NR5A2), a master regulator of cholesterol homeostasis in mammals. Our study suggests that interactions between LRH1 and Prox1 may fulfil roles both during development of the enterohepatic system and in adult physiology of the liver.
引用
收藏
页码:613 / 619
页数:7
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