生物
视网膜
计算生物学
转录组
基因
神经科学
基因表达
细胞生物学
遗传学
生物化学
作者
Karthik Shekhar,Sylvain W. Lapan,Irene E. Whitney,Nicholas M. Tran,Evan Z. Macosko,Monika S. Kowalczyk,Xian Adiconis,Joshua Z. Levin,James Nemesh,Melissa Goldman,Steven A. McCarroll,Constance L. Cepko,Aviv Regev,Joshua R. Sanes
出处
期刊:Cell
[Cell Press]
日期:2016-08-01
卷期号:166 (5): 1308-1323.e30
被引量:1175
标识
DOI:10.1016/j.cell.2016.07.054
摘要
Patterns of gene expression can be used to characterize and classify neuronal types. It is challenging, however, to generate taxonomies that fulfill the essential criteria of being comprehensive, harmonizing with conventional classification schemes, and lacking superfluous subdivisions of genuine types. To address these challenges, we used massively parallel single-cell RNA profiling and optimized computational methods on a heterogeneous class of neurons, mouse retinal bipolar cells (BCs). From a population of ∼25,000 BCs, we derived a molecular classification that identified 15 types, including all types observed previously and two novel types, one of which has a non-canonical morphology and position. We validated the classification scheme and identified dozens of novel markers using methods that match molecular expression to cell morphology. This work provides a systematic methodology for achieving comprehensive molecular classification of neurons, identifies novel neuronal types, and uncovers transcriptional differences that distinguish types within a class.
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