Wurmbach E, Wech I, Preiss A
Universität Hohenheim, Institut für Genetik (240), 70593, Stuttgart, Germany.
Mech Dev. 1999 Feb;80(2):171-80. doi: 10.1016/s0925-4773(98)00212-3.
Many cell fate decisions in higher animals are based on intercellular communication governed by the Notch signaling pathway. Developmental signals received by the Notch receptor cause Suppressor of Hairless (Su(H)) mediated transcription of target genes. In Drosophila, the majority of Notch target genes known so far is located in the Enhancer of split complex (E(spl)-C), encoding small basic helix-loop-helix (bHLH) proteins that presumably act as transcriptional repressors. Here we show that the E(spl)-C contains three additional Notch responsive, non-bHLH genes: m4 and ma are structurally related, whilst m2 encodes a novel protein. All three genes depend on Su(H) for initiation and/or maintenance of transcription. The two other non-bHLH genes within the locus, m1 and m6, are unrelated to the Notch pathway: m1 might code for a protease inhibitor of the Kazal family, and m6 for a novel peptide.
高等动物中的许多细胞命运决定是基于由Notch信号通路控制的细胞间通讯。Notch受体接收到的发育信号会导致无翅抑制因子(Su(H))介导的靶基因转录。在果蝇中,迄今为止已知的大多数Notch靶基因位于分裂增强子复合体(E(spl)-C)中,该复合体编码小的碱性螺旋-环-螺旋(bHLH)蛋白,推测这些蛋白作为转录抑制因子发挥作用。在此我们表明,E(spl)-C包含另外三个Notch反应性非bHLH基因:m4和ma在结构上相关,而m2编码一种新蛋白。所有这三个基因的转录起始和/或维持都依赖于Su(H)。该位点内的另外两个非bHLH基因m1和m6与Notch信号通路无关:m1可能编码Kazal家族的一种蛋白酶抑制剂,m6编码一种新肽。