Rascle Anne, Neumann Tanja, Raschta Anne-Sarah, Neumann Astrid, Heining Eva, Kastner Juergen, Witzgall Ralph
Institute for Molecular and Cellular Anatomy, University of Regensburg, Universitaetsstrasse 31, 93053 Regensburg, Germany.
Exp Cell Res. 2009 Jan 1;315(1):76-96. doi: 10.1016/j.yexcr.2008.10.012. Epub 2008 Oct 28.
LMX1B is a LIM-homeodomain transcription factor essential for development. Putative LMX1B target genes have been identified through mouse gene targeting studies, but their identity as direct LMX1B targets remains hypothetical. We describe here the first molecular characterization of LMX1B target gene regulation. Microarray analysis using a tetracycline-inducible LMX1B expression system in HeLa cells revealed that a subset of NF-kappaB target genes, including IL-6 and IL-8, are upregulated in LMX1B-expressing cells. Inhibition of NF-kappaB activity by short interfering RNA-mediated knock-down of p65 impairs, while activation of NF-kappaB activity by TNF-alpha synergizes induction of NF-kappaB target genes by LMX1B. Chromatin immunoprecipitation demonstrated that LMX1B binds to the proximal promoter of IL-6 and IL-8 in vivo, in the vicinity of the characterized kappaB site, and that LMX1B recruitment correlates with increased NF-kappaB DNA association. IL-6 promoter-reporter assays showed that the kappaB site and an adjacent putative LMX1B binding motif are both involved in LMX1B-mediated transcription. Expression of NF-kappaB target genes is affected in the kidney of Lmx1b(-/-) knock-out mice, thus supporting the biological relevance of our findings. Together, these data demonstrate for the first time that LMX1B directly regulates transcription of a subset of NF-kappaB target genes in cooperation with nuclear p50/p65 NF-kappaB.
LMX1B是一种对发育至关重要的含LIM结构域的同源异型转录因子。通过小鼠基因靶向研究已鉴定出推测的LMX1B靶基因,但其作为直接LMX1B靶标的身份仍属假设。我们在此描述了LMX1B靶基因调控的首次分子特征。使用四环素诱导的LMX1B表达系统在HeLa细胞中进行的微阵列分析显示,包括IL-6和IL-8在内的一部分NF-κB靶基因在表达LMX1B的细胞中上调。通过短干扰RNA介导的p65敲低抑制NF-κB活性会损害这种上调,而TNF-α激活NF-κB活性则会协同增强LMX1B对NF-κB靶基因的诱导。染色质免疫沉淀表明,LMX1B在体内与IL-6和IL-8的近端启动子结合,位于特征性κB位点附近,并且LMX1B的募集与NF-κB与DNA结合的增加相关。IL-6启动子报告基因分析表明,κB位点和相邻的推测LMX1B结合基序均参与LMX1B介导的转录。NF-κB靶基因的表达在Lmx1b(-/-)基因敲除小鼠的肾脏中受到影响,从而支持了我们研究结果的生物学相关性。总之,这些数据首次证明LMX1B与核p50/p65 NF-κB协同直接调节一部分NF-κB靶基因的转录。