Zheng Limin, Carthew Richard W
Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208, USA.
Mech Dev. 2008 Jan-Feb;125(1-2):18-29. doi: 10.1016/j.mod.2007.10.007. Epub 2007 Oct 22.
Lola is a transcription repressor that regulates axon guidance in the developing embryonic nervous system of Drosophila. Here, we show that Lola regulates two binary cell fate decisions guided by Notch inductive signaling in the developing eye: the R3-R4 and the R7-cone cell fate choices. Lola is required cell-autonomously in R3 for its specification, and Lola transforms R4 into R3 if overexpressed. Lola also promotes R7 fate at the expense of cone cell fate. Lola antagonizes Notch-dependent gene expression and Notch-dependent fate transformation. Expression analysis shows that Lola is constitutively present in all photoreceptors and cone cells. We propose that when a precursor cell receives a weak Notch inductive signal, it is not sufficiently strong to overcome the constitutive repression of target gene transcription by Lola. A precursor that receives a strong Notch inductive signal expresses target genes despite a constitutive repression by Lola. The predicted consequence of this mechanism is to sharpen a cell's responsiveness to Notch signaling by creating a threshold.
洛拉(Lola)是一种转录抑制因子,在果蝇胚胎发育中的神经系统中调节轴突导向。在此,我们表明洛拉在发育中的眼睛中通过Notch诱导信号调控两个二元细胞命运决定:R3-R4和R7-视锥细胞命运选择。在R3中,洛拉对于其细胞特化是细胞自主必需的,并且如果过度表达,洛拉会将R4转化为R3。洛拉还以视锥细胞命运为代价促进R7命运。洛拉拮抗Notch依赖性基因表达和Notch依赖性命运转变。表达分析表明,洛拉在所有光感受器和视锥细胞中组成性存在。我们提出,当前体细胞接收到微弱的Notch诱导信号时,该信号强度不足以克服洛拉对靶基因转录的组成性抑制。尽管受到洛拉的组成性抑制,但接收到强Notch诱导信号的前体细胞仍会表达靶基因。这种机制的预期结果是通过创建一个阈值来增强细胞对Notch信号的反应性。