Transcriptional code and disease map for adult retinal cell types

被引:207
作者
Siegert, Sandra [1 ]
Cabuy, Erik [1 ]
Scherf, Brigitte Gross [1 ]
Kohler, Hubertus [1 ]
Panda, Satchidananda [2 ]
Le, Yun-Zheng [3 ,4 ]
Fehling, Hans Joerg [5 ]
Gaidatzis, Dimos [1 ,6 ]
Stadler, Michael B. [1 ,6 ]
Roska, Botond [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, Neural Circuit Labs, Basel, Switzerland
[2] Salk Inst Biol Studies, Regulatory Biol Lab, La Jolla, CA 92037 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Oklahoma City, OK USA
[4] Univ Oklahoma, Hlth Sci Ctr, Harold Hamm Oklahoma Diabet Ctr, Oklahoma City, OK USA
[5] Univ Clin Ulm, Inst Immunol, Ulm, Germany
[6] Swiss Inst Bioinformat, Basel, Switzerland
基金
欧洲研究理事会;
关键词
MACULAR DEGENERATION; GENE-EXPRESSION; IN-VIVO; DOPAMINERGIC-NEURONS; ALZHEIMERS-DISEASE; HUMAN FIBROBLASTS; COMMON VARIANTS; AMACRINE CELLS; MOUSE; PHOTOTRANSDUCTION;
D O I
10.1038/nn.3032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Brain circuits are assembled from a large variety of morphologically and functionally diverse cell types. It is not known how the intermingled cell types of an individual adult brain region differ in their expressed genomes. Here we describe an atlas of cell type transcriptomes in one brain region, the mouse retina. We found that each adult cell type expressed a specific set of genes, including a unique set of transcription factors, forming a 'barcode' for cell identity. Cell type transcriptomes carried enough information to categorize cells into morphological classes and types. Several genes that were specifically expressed in particular retinal circuit elements, such as inhibitory neuron types, are associated with eye diseases. The resource described here allows gene expression to be compared across adult retinal cell types, experimenting with specific transcription factors to differentiate stem or somatic cells to retinal cell types, and predicting cellular targets of newly discovered disease-associated genes.
引用
收藏
页码:487 / U191
页数:11
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