Kugler Sabrina J, Nagel Anja C
Institute of Genetics (240), University of Hohenheim, 70599 Stuttgart, Germany.
Mol Biol Cell. 2007 Oct;18(10):3733-40. doi: 10.1091/mbc.e07-03-0263. Epub 2007 Jul 18.
We have identified the gene putzig (pzg) as a key regulator of cell proliferation and of Notch signaling in Drosophila. pzg encodes a Zn-finger protein that was found earlier within a macromolecular complex, including TATA-binding protein-related factor 2 (TRF2)/DNA replication-related element factor (DREF). This complex is involved in core promoter selection, where DREF functions as a transcriptional activator of replication-related genes. Here, we provide the first in vivo evidence that pzg is required for the expression of cell cycle and replication-related genes, and hence for normal developmental growth. Independent of its role in the TRF2/DREF complex, pzg acts as a positive regulator of Notch signaling that may occur by chromatin activation. Down-regulation of pzg activity inhibits Notch target gene activation, whereas Hedgehog (Hh) signal transduction and growth regulation are unaffected. Our findings uncover different modes of operation of pzg during imaginal development of Drosophila, and they provide a novel mechanism of Notch regulation.
我们已确定果蝇中的putzig(pzg)基因是细胞增殖和Notch信号传导的关键调节因子。pzg编码一种锌指蛋白,该蛋白先前在一个大分子复合物中被发现,该复合物包括TATA结合蛋白相关因子2(TRF2)/DNA复制相关元件因子(DREF)。这个复合物参与核心启动子的选择,其中DREF作为复制相关基因的转录激活因子发挥作用。在这里,我们提供了首个体内证据,表明pzg是细胞周期和复制相关基因表达所必需的,因此对于正常的发育生长也是必需的。独立于其在TRF2/DREF复合物中的作用,pzg作为Notch信号传导的正调节因子,可能通过染色质激活而发生。pzg活性的下调会抑制Notch靶基因的激活,而Hedgehog(Hh)信号转导和生长调节不受影响。我们的研究结果揭示了pzg在果蝇成虫发育过程中的不同作用模式,并提供了一种新的Notch调节机制。