Frontini Mattia, Imbriano Carol, Manni Isabella, Mantovani Roberto
Dipartimento di Biologia Animale; Universita di Modena e Reggio Emilia, Modena, Italy.
Cell Cycle. 2004 Feb;3(2):217-22.
NF-Y is a trimeric activator with histone fold, HFM, subunits that binds to the CCAAT-box and is required for a majority of cell cycle promoters, often in conjunction with E2Fs. In vivo binding of NF-Y is dynamic during the cell cycle and correlates with gene activation. We performed immunofluorescence studies on endogenous, GFP- and Flag-tagged overexpressed NF-Y subunits. NF-YA, NF-YB are nuclear proteins. Unexpectedly, NF-YC localizes both in cytoplamatic and nuclear compartments and its nuclear localization is determined by the interaction with its heterodimerization partner NF-YB. Most importantly, compartmentalization is regulated during the cell cycle of serum restimulated NIH3T3 cells, accumulating in the nucleus at the onset of S phase. These data point to the control of HFM heterodimerization as an important layer of NF-Y regulation during cell cycle progression.
核因子Y(NF-Y)是一种具有组蛋白折叠(HFM)亚基的三聚体激活因子,它与CCAAT框结合,是大多数细胞周期启动子所必需的,通常与E2F因子协同作用。在体内,NF-Y在细胞周期中的结合是动态的,并且与基因激活相关。我们对内源的、绿色荧光蛋白(GFP)标记和Flag标记的过表达NF-Y亚基进行了免疫荧光研究。NF-YA和NF-YB是核蛋白。出乎意料的是,NF-YC定位于细胞质和细胞核区室,其核定位由与其异二聚体伙伴NF-YB的相互作用决定。最重要的是,在血清再刺激的NIH3T3细胞的细胞周期中,区室化受到调控,在S期开始时在细胞核中积累。这些数据表明,在细胞周期进程中,HFM异二聚化的控制是NF-Y调控的一个重要层面。