Department of Ophthalmology, Emory University, 1365B Clifton Road NE Atlanta GA, 30322.
Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, 71 S Manassas St, Memphis TN 38163.
Mol Vis. 2020 Mar 6;26:173-187. eCollection 2020.
We illustrate the growing power of the BXD family of mice (recombinant inbred strains from a cross of C57BL/6J and DBA/2J mice) and companion bioinformatic tools to study complex genome-phenome relations related to glaucoma. Over the past 16 years, our group has integrated powerful murine resources and web-accessible tools to identify networks modulating visual system traits-from photoreceptors to the visual cortex. Recent studies focused on retinal ganglion cells and glaucoma risk factors, including intraocular pressure (IOP), central corneal thickness (CCT), and susceptibility of cellular stress. The BXD family was exploited to define key gene variants and then establish linkage to glaucoma in human cohorts. The power of this experimental approach to precision medicine is highlighted by recent studies that defined cadherin 11 () and a calcium channel () as genes modulating IOP, as a genetic link between CCT and retinal ganglion cell (RGC) death, and as a gene that modulates the susceptibility of RGCs to death after elevated IOP. The role of three of these gene variants in glaucoma is discussed, along with the pathways activated in the disease process.
我们展示了 BXD 系小鼠(C57BL/6J 和 DBA/2J 杂交的重组近交系)及其配套生物信息学工具在研究与青光眼相关的复杂基因组-表型关系方面日益增强的力量。在过去的 16 年中,我们的团队整合了强大的小鼠资源和可访问的网络工具,以鉴定从光感受器到视皮层的视觉系统特征的调节网络。最近的研究集中在视网膜神经节细胞和青光眼风险因素上,包括眼压(IOP)、中央角膜厚度(CCT)和细胞应激易感性。BXD 系被用于确定关键的基因变异,然后在人类队列中建立与青光眼的关联。最近的研究强调了这种精准医学实验方法的力量,这些研究确定了钙黏蛋白 11()和钙通道()作为调节眼压的基因,作为 CCT 和视网膜神经节细胞(RGC)死亡之间的遗传联系,以及作为调节 RGC 在高眼压后易感性的基因。讨论了这三个基因变异在青光眼中的作用,以及疾病过程中激活的途径。