Jump D B, Badin M V, Thelen A
Department of Physiology, Michigan State University, East Lansing, Michigan 48824, USA.
J Biol Chem. 1997 Oct 31;272(44):27778-86. doi: 10.1074/jbc.272.44.27778.
Triiodothyronine (T3) activates rat liver S14 gene transcription through T3 receptors (TRbeta) binding distal thyroid hormone response elements located between -2.8 and -2.5 kilobase pairs upstream from the transcription start site. Previous studies suggested that proximal promoter elements located between -220 to -80 base pairs upstream from the 5' end of the S14 gene were involved in hormone activation of the S14 gene. This report identifies an inverted CCAAT box (or Y box) at -104ATTGG-100 as a core cis-regulatory element. Gel shift studies using rat liver nuclear proteins show that at least three CCAAT-binding factors interact with this region as follows: NF-Y and c/EBP-related proteins formed major complexes, whereas NF-1/CTF forms a minor complex in gel shift assay. Mutation of the Y box indicated that loss of NF-Y binding, but not c/EBP or NF-1, correlated closely with a decline in basal activity and a loss of T3-mediated transactivation. Substitution of the S14 Y box in reporter genes with elements binding only NF-Y elevated basal activity and T3-mediated transactivation, whereas substitution with elements binding c/EBP-related proteins or SP1 displayed low basal activity and T3-mediated transactivation. These studies indicate that NF-Y and TRbeta functionally interact to confer T3 control to the S14 gene.
三碘甲状腺原氨酸(T3)通过T3受体(TRβ)与位于转录起始位点上游-2.8至-2.5千碱基对之间的远端甲状腺激素反应元件结合,从而激活大鼠肝脏S14基因转录。先前的研究表明,位于S14基因5'端上游-220至-80碱基对之间的近端启动子元件参与了S14基因的激素激活过程。本报告鉴定出位于-104ATTGG-100处的一个反向CCAAT盒(或Y盒)作为核心顺式调控元件。使用大鼠肝脏核蛋白进行的凝胶迁移研究表明,至少有三种CCAAT结合因子与该区域相互作用,具体如下:NF-Y和c/EBP相关蛋白形成主要复合物,而NF-1/CTF在凝胶迁移试验中形成次要复合物。Y盒的突变表明,NF-Y结合的丧失而非c/EBP或NF-1的丧失与基础活性的下降和T3介导的反式激活的丧失密切相关。用仅结合NF-Y的元件替换报告基因中的S14 Y盒可提高基础活性和T3介导的反式激活,而用结合c/EBP相关蛋白或SP1的元件替换则显示出低基础活性和T3介导的反式激活。这些研究表明,NF-Y和TRβ在功能上相互作用,赋予S14基因T3调控能力。