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本文引用的文献

1
Identification of diverse astrocyte populations and their malignant analogs.不同星形胶质细胞群体及其恶性类似物的鉴定。
Nat Neurosci. 2017 Mar;20(3):396-405. doi: 10.1038/nn.4493. Epub 2017 Feb 6.
2
Highly Efficient Genome Editing of Murine and Human Hematopoietic Progenitor Cells by CRISPR/Cas9.利用CRISPR/Cas9对小鼠和人类造血祖细胞进行高效基因组编辑
Cell Rep. 2016 Oct 25;17(5):1453-1461. doi: 10.1016/j.celrep.2016.09.092.
3
Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma.分子分析揭示弥漫性胶质瘤的生物学离散亚群和进展途径。
Cell. 2016 Jan 28;164(3):550-63. doi: 10.1016/j.cell.2015.12.028.
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Getting the genome in shape: the formation of loops, domains and compartments.塑造基因组:环、结构域和区室的形成。
Genome Biol. 2015 Aug 10;16(1):154. doi: 10.1186/s13059-015-0730-1.
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Three-dimensional genome architecture: players and mechanisms.三维基因组结构:参与者和机制。
Nat Rev Mol Cell Biol. 2015 Apr;16(4):245-57. doi: 10.1038/nrm3965. Epub 2015 Mar 11.
6
Genetics and epigenetics of gliomas.神经胶质瘤的遗传学与表观遗传学
Swiss Med Wkly. 2014 Oct 30;144:w14018. doi: 10.4414/smw.2014.14018. eCollection 2014.
7
Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes.Sox10与NFIA之间的相互拮抗作用调节神经胶质谱系和胶质瘤亚型的多样化。
Nat Neurosci. 2014 Oct;17(10):1322-9. doi: 10.1038/nn.3790. Epub 2014 Aug 24.
8
CRISPR-mediated direct mutation of cancer genes in the mouse liver.CRISPR介导的小鼠肝脏中癌症基因的直接突变。
Nature. 2014 Oct 16;514(7522):380-4. doi: 10.1038/nature13589. Epub 2014 Aug 6.
9
Transcriptional enhancers: from properties to genome-wide predictions.转录增强子:从特性到全基因组预测。
Nat Rev Genet. 2014 Apr;15(4):272-86. doi: 10.1038/nrg3682. Epub 2014 Mar 11.
10
How to make spinal motor neurons.如何生成脊髓运动神经元。
Development. 2014 Feb;141(3):491-501. doi: 10.1242/dev.097410.

神经胶质细胞特异性增强子和染色质结构调节NFIA表达和胶质瘤肿瘤发生。

Glia-specific enhancers and chromatin structure regulate NFIA expression and glioma tumorigenesis.

作者信息

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

机构信息

Center for Cell and Gene Therapy, Baylor College of Medicine, Houston, Texas, USA.

Program in Developmental Biology, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Nat Neurosci. 2017 Nov;20(11):1520-1528. doi: 10.1038/nn.4638. Epub 2017 Sep 11.

DOI:10.1038/nn.4638
PMID:28892058
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5919190/
Abstract

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.

摘要

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。