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本文引用的文献

1
Biology and therapy of inherited retinal degenerative disease: insights from mouse models.遗传性视网膜退行性疾病的生物学与治疗:来自小鼠模型的见解
Dis Model Mech. 2015 Feb;8(2):109-29. doi: 10.1242/dmm.017913.
2
A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping.一份碱基对分辨率的人类基因组三维图谱揭示了染色质环化的原理。
Cell. 2014 Dec 18;159(7):1665-80. doi: 10.1016/j.cell.2014.11.021. Epub 2014 Dec 11.
3
rMATS: robust and flexible detection of differential alternative splicing from replicate RNA-Seq data.rMATS:从重复RNA测序数据中稳健且灵活地检测差异可变剪接
Proc Natl Acad Sci U S A. 2014 Dec 23;111(51):E5593-601. doi: 10.1073/pnas.1419161111. Epub 2014 Dec 5.
4
DNA methylation and differential gene regulation in photoreceptor cell death.光感受器细胞死亡中的DNA甲基化与基因差异调控。
Cell Death Dis. 2014 Dec 4;5(12):e1558. doi: 10.1038/cddis.2014.512.
5
Diverse epigenetic mechanisms of human disease.人类疾病的多种表观遗传机制。
Annu Rev Genet. 2014;48:237-68. doi: 10.1146/annurev-genet-120213-092518. Epub 2014 Sep 5.
6
Aryl hydrocarbon receptor knock-out exacerbates choroidal neovascularization via multiple pathogenic pathways.芳烃受体基因敲除通过多种致病途径加剧脉络膜新生血管形成。
J Pathol. 2015 Jan;235(1):101-12. doi: 10.1002/path.4433. Epub 2014 Oct 10.
7
Deletion of aryl hydrocarbon receptor AHR in mice leads to subretinal accumulation of microglia and RPE atrophy.小鼠中芳烃受体AHR的缺失导致小胶质细胞在视网膜下积聚和视网膜色素上皮萎缩。
Invest Ophthalmol Vis Sci. 2014 Aug 26;55(9):6031-40. doi: 10.1167/iovs.14-15091.
8
A framework for the interpretation of de novo mutation in human disease.一种人类疾病中新生突变的解读框架。
Nat Genet. 2014 Sep;46(9):944-50. doi: 10.1038/ng.3050. Epub 2014 Aug 3.
9
Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity.单细胞全基因组亚硫酸氢盐测序评估表观遗传异质性。
Nat Methods. 2014 Aug;11(8):817-820. doi: 10.1038/nmeth.3035. Epub 2014 Jul 20.
10
Cellular responses following retinal injuries and therapeutic approaches for neurodegenerative diseases.视网膜损伤后的细胞反应和神经退行性疾病的治疗方法。
Prog Retin Eye Res. 2014 Nov;43:17-75. doi: 10.1016/j.preteyeres.2014.07.001. Epub 2014 Jul 17.

新一代测序技术带来的视野:用于构建视网膜发育、衰老和疾病相关基因调控网络的全基因组多维分析

Vision from next generation sequencing: multi-dimensional genome-wide analysis for producing gene regulatory networks underlying retinal development, aging and disease.

作者信息

Yang Hyun-Jin, Ratnapriya Rinki, Cogliati Tiziana, Kim Jung-Woong, Swaroop Anand

机构信息

Neurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, 6 Center Drive, Bethesda, MD 20892-0610, USA.

Neurobiology-Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, 6 Center Drive, Bethesda, MD 20892-0610, USA.

出版信息

Prog Retin Eye Res. 2015 May;46:1-30. doi: 10.1016/j.preteyeres.2015.01.005. Epub 2015 Feb 7.

DOI:10.1016/j.preteyeres.2015.01.005
PMID:25668385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4402139/
Abstract

Genomics and genetics have invaded all aspects of biology and medicine, opening uncharted territory for scientific exploration. The definition of "gene" itself has become ambiguous, and the central dogma is continuously being revised and expanded. Computational biology and computational medicine are no longer intellectual domains of the chosen few. Next generation sequencing (NGS) technology, together with novel methods of pattern recognition and network analyses, has revolutionized the way we think about fundamental biological mechanisms and cellular pathways. In this review, we discuss NGS-based genome-wide approaches that can provide deeper insights into retinal development, aging and disease pathogenesis. We first focus on gene regulatory networks (GRNs) that govern the differentiation of retinal photoreceptors and modulate adaptive response during aging. Then, we discuss NGS technology in the context of retinal disease and develop a vision for therapies based on network biology. We should emphasize that basic strategies for network construction and analyses can be transported to any tissue or cell type. We believe that specific and uniform guidelines are required for generation of genome, transcriptome and epigenome data to facilitate comparative analysis and integration of multi-dimensional data sets, and for constructing networks underlying complex biological processes. As cellular homeostasis and organismal survival are dependent on gene-gene and gene-environment interactions, we believe that network-based biology will provide the foundation for deciphering disease mechanisms and discovering novel drug targets for retinal neurodegenerative diseases.

摘要

基因组学和遗传学已经渗透到生物学和医学的各个方面,为科学探索开辟了未知领域。“基因”本身的定义已经变得模糊不清,中心法则也在不断修订和扩展。计算生物学和计算医学不再是少数人的知识领域。下一代测序(NGS)技术,连同模式识别和网络分析的新方法,彻底改变了我们对基本生物学机制和细胞通路的思考方式。在这篇综述中,我们讨论基于NGS的全基因组方法,这些方法可以更深入地了解视网膜发育、衰老和疾病发病机制。我们首先关注调控视网膜光感受器分化并调节衰老过程中适应性反应的基因调控网络(GRN)。然后,我们在视网膜疾病的背景下讨论NGS技术,并基于网络生物学提出治疗愿景。我们应该强调,网络构建和分析的基本策略可以应用于任何组织或细胞类型。我们认为,为了便于对多维数据集进行比较分析和整合,以及构建复杂生物学过程的基础网络,生成基因组、转录组和表观基因组数据需要特定且统一的指导方针。由于细胞内稳态和机体存活依赖于基因-基因和基因-环境相互作用,我们相信基于网络的生物学将为解读视网膜神经退行性疾病的发病机制和发现新的药物靶点提供基础。