Wood Jamie L, Nepal Saroj, Jones Bradley W
Department of Biology, The University of Mississippi, University, MS, 38677, USA.
Department of Medical Education, Duke University School of Medicine, Durham, NC, 27710, USA.
Sci Rep. 2025 Jan 7;15(1):1238. doi: 10.1038/s41598-025-85247-0.
During development, cells of the nervous system begin as unspecified precursors and proceed along one of two developmental paths to become either neurons or glia. Work in the fruit fly Drosophila melanogaster has established the role of the transcription factor Glial cells missing (Gcm) in directing neuronal precursor cells to assume a glial cell fate. Gcm acts on many target genes, one of which is reversed polarity (repo). repo encodes a homeodomain transcription factor and is necessary for the terminal differentiation of glial cells. Transient Gcm expression is followed by maintained expression of repo. Evidence supports autoregulation to be one of the mechanisms that maintains repo expression, as ectopic repo expression in embryos can activate repo-lacZ reporter constructs. In this paper we further explore the ability of repo to activate reporter constructs in transgenic embryos and in cultured S2 cells. We provide further evidence that Repo protein acts as a transcription factor on its own regulatory DNA sequence. We report that three canonical Repo binding sites (RBSs) are located within the upstream 4.3 kilobase repo cis-regulatory DNA (CRD). The upstream 2 kb within the repo CRD has remarkable repo-dependent gene expression activity, and mutagenesis of RBS1 in this 2 kb region results in a significant decrease in repo-induced reporter gene expression in both systems. Our results in cell culture experiments also show that RBS2 and/or RBS3 can affect repo-dependent gene expression in the context of the whole upstream repo CRD. Mutagenesis of both RBS2 and RBS3 in the repo CRD, leaving RBS1 intact, significantly reduces repo-induced reporter gene expression. These results suggest that all three canonical RBSs may be cooperatively involved in autoregulation of repo expression.
在发育过程中,神经系统的细胞最初是未分化的前体细胞,然后沿着两条发育途径之一发展,成为神经元或神经胶质细胞。在果蝇黑腹果蝇中的研究确定了转录因子神经胶质细胞缺失(Gcm)在引导神经元前体细胞转变为神经胶质细胞命运中的作用。Gcm作用于许多靶基因,其中之一是反向极性(repo)。repo编码一个同源结构域转录因子,是神经胶质细胞终末分化所必需的。短暂的Gcm表达之后是repo的持续表达。有证据支持自我调节是维持repo表达的机制之一,因为胚胎中异位的repo表达可以激活repo-lacZ报告基因构建体。在本文中,我们进一步探索了repo在转基因胚胎和培养的S2细胞中激活报告基因构建体的能力。我们提供了进一步的证据,表明Repo蛋白在其自身的调控DNA序列上作为转录因子发挥作用。我们报告说,三个典型的Repo结合位点(RBSs)位于上游4.3千碱基的repo顺式调控DNA(CRD)内。repo CRD内的上游2 kb具有显著的依赖于repo的基因表达活性,并且在该2 kb区域中RBS1的诱变导致两个系统中repo诱导的报告基因表达显著降低。我们在细胞培养实验中的结果还表明,在整个上游repo CRD的背景下,RBS2和/或RBS3可以影响依赖于repo的基因表达。在repo CRD中对RBS2和RBS3进行诱变,使RBS1保持完整,会显著降低repo诱导的报告基因表达。这些结果表明,所有三个典型的RBSs可能共同参与repo表达的自我调节。