Glasgow Stacey M, Carlson Jeffrey C, Zhu Wenyi, Chaboub Lesley S, Kang Peng, Lee Hyun Kyoung, Clovis Yoanne M, Lozzi Brittney E, McEvilly Robert J, Rosenfeld Michael G, Creighton Chad J, Lee Soo-Kyung, Mohila Carrie A, Deneen Benjamin
Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas, USA.
Program in Developmental Biology, Baylor College of Medicine, Houston, Texas, USA.
Nat Neurosci. 2017 Nov;20(11):1520-1528. doi: 10.1038/nn.4638. Epub 2017 Sep 11.
Long-range enhancer interactions critically regulate gene expression, yet little is known about how their coordinated activities contribute to CNS development or how this may, in turn, relate to disease states. By examining the regulation of the transcription factor NFIA in the developing spinal cord, we identified long-range enhancers that recapitulate NFIA expression across glial and neuronal lineages in vivo. Complementary genetic studies found that Sox9-Brn2 and Isl1-Lhx3 regulate enhancer activity and NFIA expression in glial and neuronal populations. Chromatin conformation analysis revealed that these enhancers and transcription factors form distinct architectures within these lineages in the spinal cord. In glioma models, the glia-specific architecture is present in tumors, and these enhancers are required for NFIA expression and contribute to glioma formation. By delineating three-dimensional mechanisms of gene expression regulation, our studies identify lineage-specific chromatin architectures and associated enhancers that regulate cell fate and tumorigenesis in the CNS.
远距离增强子相互作用对基因表达起着关键的调控作用,但对于它们的协同活动如何促进中枢神经系统发育,或者这又如何反过来与疾病状态相关,我们却知之甚少。通过研究发育中的脊髓中转录因子NFIA的调控机制,我们鉴定出了一些远距离增强子,这些增强子在体内能够重现NFIA在神经胶质细胞和神经元谱系中的表达情况。互补的遗传学研究发现,Sox9-Brn2和Isl1-Lhx3调节神经胶质细胞和神经元群体中的增强子活性以及NFIA表达。染色质构象分析表明,这些增强子和转录因子在脊髓的这些谱系中形成了不同的结构。在胶质瘤模型中,神经胶质细胞特异性结构存在于肿瘤中,并且这些增强子是NFIA表达所必需的,并且有助于胶质瘤的形成。通过描绘基因表达调控的三维机制,我们的研究确定了在中枢神经系统中调节细胞命运和肿瘤发生的谱系特异性染色质结构及相关增强子。