Laboratory for Molecular Biology, Department of Biological Sciences, University of Illinois at Chicago, 900S. Ashland Avenue (MC567), Chicago, IL 60607, USA.
Dev Biol. 2013 Oct 1;382(1):38-47. doi: 10.1016/j.ydbio.2013.08.001. Epub 2013 Aug 8.
T-box genes are frequently expressed in dynamic patterns during animal development, but the mechanisms controlling expression of these genes are not well understood. The Caenorhabditis elegans T-box gene tbx-2 is essential for development of the ABa-derived pharyngeal muscles, specification of neural cell fate in the HSN/PHB lineage, and adaptation in olfactory neurons. The tbx-2 expression pattern is complex, and expression has been described in pharyngeal precursors and body wall muscles during embryogenesis, and amphid sensory neurons and pharyngeal neurons in adults. To examine mechanisms regulating tbx-2 gene expression, we performed an RNAi screen of transcription factor genes in strains containing a Ptbx-2::gfp reporter and identified the Nuclear Factor Y (NF-Y) complex as a negative regulator of tbx-2 expression. NF-Y is a heterotrimeric CCAAT-binding complex consisting of A-C subunits, and reduction of the NF-Y subunits nfya-1, nfyb-1, or nfyc-1 by RNAi or using mutants results in ectopic Ptbx-2::gfp expression in hypodermal seam cells and gut. Mutation of two CCAAT-boxes in the tbx-2 promoter results in a similar pattern of ectopic Ptbx-2::gfp expression, suggesting NF-Y directly represses the tbx-2 promoter. tbx-2 mRNA is moderately increased in nfya-1 null mutants, indicating NF-Y represses expression of endogenous tbx-2. Finally we identify and characterize a second-site mutation that enhances lethality of a temperature sensitive tbx-2 mutant and show that this mutation is a deletion in the nfyb-1 gene. Together, these results identify NF-Y as an important regulator of tbx-2 function in vivo.
T 盒基因在动物发育过程中经常以动态模式表达,但控制这些基因表达的机制尚不清楚。秀丽隐杆线虫 T 盒基因 tbx-2 对于 ABa 衍生的咽肌发育、HSN/PHB 谱系中神经细胞命运的特化以及嗅觉神经元的适应是必不可少的。tbx-2 的表达模式很复杂,在胚胎发生过程中,在咽前体和体壁肌肉中以及在成体的触角感觉神经元和咽神经元中都有描述。为了研究调节 tbx-2 基因表达的机制,我们在含有 Ptbx-2::gfp 报告基因的菌株中进行了转录因子基因的 RNAi 筛选,并鉴定出核因子 Y(NF-Y)复合物作为 tbx-2 表达的负调节剂。NF-Y 是一种 CCAAT 结合的异三聚体复合物,由 A-C 亚基组成,通过 RNAi 或使用突变体减少 NF-Y 亚基 nfya-1、nfyb-1 或 nfyc-1 会导致 Ptbx-2::gfp 在真皮节细胞和肠道中异位表达。tbx-2 启动子中两个 CCAAT 盒的突变会导致类似的 Ptbx-2::gfp 异位表达模式,表明 NF-Y 直接抑制 tbx-2 启动子。nfya-1 缺失突变体中 tbx-2 mRNA 中度增加,表明 NF-Y 抑制内源性 tbx-2 的表达。最后,我们鉴定并表征了一个增强温度敏感 tbx-2 突变体致死性的第二点突变,并表明该突变是 nfyb-1 基因的缺失。总之,这些结果表明 NF-Y 是体内 tbx-2 功能的重要调节剂。