School of Biosciences, Cardiff University, Cardiff CF10 3AX, Wales, United Kingdom.
J Biol Chem. 2011 Apr 29;286(17):15227-39. doi: 10.1074/jbc.M110.201996. Epub 2011 Mar 2.
FRA-2/FOSL2 is a basic region-leucine zipper motif transcription factor that is widely expressed in mammalian tissues. The functional repertoire of this factor is unclear, partly due to a lack of knowledge of genomic sequences that are targeted. Here, we identified novel, functional FRA-2 targets across the genome through expression profile analysis in a knockdown transgenic rat. In this model, a nocturnal rhythm of pineal gland FRA-2 is suppressed by a genetically encoded, dominant negative mutant protein. Bioinformatic analysis of validated sets of FRA-2-regulated and -nonregulated genes revealed that the FRA-2 regulon is limited by genomic target selection rules that, in general, transcend core cis-sequence identity. However, one variant AP-1-related (AP-1R) sequence was common to a subset of regulated genes. The functional activity and protein binding partners of a candidate AP-1R sequence were determined for a novel FRA-2-repressed gene, Rgs4. FRA-2 protein preferentially associated with a proximal Rgs4 AP-1R sequence as demonstrated by ex vivo ChIP and in vitro EMSA analysis; moreover, transcriptional repression was blocked by mutation of the AP-1R sequence, whereas mutation of an upstream consensus AP-1 family sequence did not affect Rgs4 expression. Nocturnal changes in protein complexes at the Rgs4 AP-1R sequence are associated with FRA-2-dependent dismissal of the co-activator, CBP; this provides a mechanistic basis for Rgs4 gene repression. These studies have also provided functional insight into selective genomic targeting by FRA-2, highlighting discordance between predicted and actual targets. Future studies should address FRA-2-Rgs4 interactions in other systems, including the brain, where FRA-2 function is poorly understood.
FRA-2/FOSL2 是一种广泛表达于哺乳动物组织中的碱性亮氨酸拉链基序转录因子。该因子的功能谱尚不清楚,部分原因是缺乏靶向的基因组序列知识。在这里,我们通过在敲低转基因大鼠中的表达谱分析,鉴定了全基因组中的新型、功能性 FRA-2 靶标。在该模型中,由遗传编码的显性负突变蛋白抑制了松果腺 FRA-2 的昼夜节律。经过验证的 FRA-2 调控和非调控基因集的生物信息学分析表明,FRA-2 调控子受基因组靶标选择规则的限制,这些规则通常超越核心顺式序列同一性。然而,一个变体 AP-1 相关 (AP-1R) 序列是受调控基因子集共有的。候选 AP-1R 序列的功能活性和蛋白质结合伴侣是通过对一种新型 FRA-2 抑制基因 Rgs4 进行测定的。FRA-2 蛋白与候选 Rgs4 AP-1R 序列的近端优先结合,这一点通过离体 ChIP 和体外 EMSA 分析得到了证明;此外,AP-1R 序列的突变阻止了转录抑制,而上游共识 AP-1 家族序列的突变则不影响 Rgs4 的表达。在 Rgs4 AP-1R 序列处,昼夜变化的蛋白质复合物与 FRA-2 依赖性的 CBP 共激活因子的解雇有关;这为 Rgs4 基因抑制提供了机制基础。这些研究还为 FRA-2 对选择性基因组靶标的功能见解提供了依据,突出了预测靶标与实际靶标之间的差异。未来的研究应该在其他系统(包括大脑)中研究 FRA-2-Rgs4 相互作用,因为在大脑中 FRA-2 功能尚不清楚。