Jiménez G, Guichet A, Ephrussi A, Casanova J
Institut de Biologia Molecular de Barcelona (CSIC), 08034 Barcelona, Spain.
Genes Dev. 2000 Jan 15;14(2):224-31.
Differentiation of the embryonic termini in Drosophila depends on signaling by the Tor RTK, which induces terminal gene expression by inactivating at the embryonic poles a uniformly distributed repressor activity that involves the Gro corepressor. Here, we identify a new gene, cic, that acts as a repressor of terminal genes regulated by the Tor pathway. cic also mediates repression along the dorsoventral axis, a process that requires the Dorsal morphogen and Gro, and which is also inhibited by Tor signaling at the termini. cic encodes an HMG-box transcription factor that interacts with Gro in vitro. We present evidence that Tor signaling regulates terminal patterning by inactivating Cic at the embryo poles. cic has been evolutionarily conserved, suggesting that Cic-like proteins may act as repressors regulated by RTK signaling in other organisms.
果蝇胚胎两端的分化取决于Tor受体酪氨酸激酶(RTK)的信号传导,该信号传导通过在胚胎两极使一种涉及Gro共抑制因子的均匀分布的阻遏活性失活来诱导末端基因表达。在这里,我们鉴定出一个新基因cic,它作为由Tor信号通路调控的末端基因的阻遏物。cic还介导沿背腹轴的抑制作用,这一过程需要背侧形态发生素和Gro,并且在两端也受到Tor信号传导的抑制。cic编码一种在体外与Gro相互作用的HMG盒转录因子。我们提供的证据表明,Tor信号传导通过使胚胎两极的Cic失活来调节末端模式形成。cic在进化上是保守的,这表明类似Cic的蛋白质可能在其他生物体中作为受RTK信号传导调控的阻遏物发挥作用。