Ross Jermaine, Kuzin Alexander, Brody Thomas, Odenwald Ward F
Neural Cell-Fate Determinants Section, NINDS, NIH, Bethesda, Maryland.
Genesis. 2018 Aug;56(8):e23237. doi: 10.1002/dvg.23237. Epub 2018 Aug 18.
While developmental studies of Drosophila neural stem cell lineages have identified transcription factors (TFs) important to cell identity decisions, currently only an incomplete understanding exists of the cis-regulatory elements that control the dynamic expression of these TFs. Our previous studies have identified multiple enhancers that regulate the POU-domain TF paralogs nubbin and pdm-2 genes. Evolutionary comparative analysis of these enhancers reveals that they each contain multiple conserved sequence blocks (CSBs) that span TF DNA-binding sites for known regulators of neuroblast (NB) gene expression in addition to novel sequences. This study functionally analyzes the conserved DNA sequence elements within a NB enhancer located within the nubbin gene and highlights a high level of complexity underlying enhancer structure. Mutational analysis has revealed CSBs that are important for enhancer activation and silencing in the developing CNS. We have also observed that adjusting the number and relative positions of the TF binding sites within these CSBs alters enhancer function.
虽然对果蝇神经干细胞谱系的发育研究已经确定了对细胞身份决定很重要的转录因子(TFs),但目前对于控制这些TFs动态表达的顺式调控元件,人们的理解还不完整。我们之前的研究已经鉴定出多个调控POU结构域TF旁系同源基因nubbin和pdm-2的增强子。对这些增强子的进化比较分析表明,它们各自包含多个保守序列块(CSBs),除了新序列外,这些保守序列块还跨越了已知的神经母细胞(NB)基因表达调控因子的TF DNA结合位点。本研究对位于nubbin基因内的一个NB增强子中的保守DNA序列元件进行了功能分析,并突出了增强子结构背后的高度复杂性。突变分析揭示了在发育中的中枢神经系统中对增强子激活和沉默很重要的CSBs。我们还观察到,调整这些CSBs内TF结合位点的数量和相对位置会改变增强子功能。