Measuring cell identity in noisy biological systems

被引:20
作者
Birnbaum, Kenneth D. [1 ]
Kussell, Edo [1 ,2 ]
机构
[1] NYU, Dept Biol, Ctr Genom & Syst Biol, New York, NY 10003 USA
[2] NYU, Dept Phys, New York, NY 10003 USA
基金
美国国家卫生研究院;
关键词
STOCHASTIC GENE-EXPRESSION; ARABIDOPSIS ROOT; MORPHOLOGICAL COMPLEXITY; CLASSIFICATION; IDENTIFICATION; DISCOVERY; CANCER; DIFFERENTIATION; INFORMATION; EVOLUTION;
D O I
10.1093/nar/gkr591
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Global gene expression measurements are increasingly obtained as a function of cell type, spatial position within a tissue and other biologically meaningful coordinates. Such data should enable quantitative analysis of the cell-type specificity of gene expression, but such analyses can often be confounded by the presence of noise. We introduce a specificity measure Spec that quantifies the information in a gene's complete expression profile regarding any given cell type, and an uncertainty measure dSpec, which measures the effect of noise on specificity. Using global gene expression data from the mouse brain, plant root and human white blood cells, we show that Spec identifies genes with variable expression levels that are nonetheless highly specific of particular cell types. When samples from different individuals are used, dSpec measures genes' transcriptional plasticity in each cell type. Our approach is broadly applicable to mapped gene expression measurements in stem cell biology, developmental biology, cancer biology and biomarker identification. As an example of such applications, we show that Spec identifies a new class of biomarkers, which exhibit variable expression without compromising specificity. The approach provides a unifying theoretical framework for quantifying specificity in the presence of noise, which is widely applicable across diverse biological systems.
引用
收藏
页码:9093 / 9107
页数:15
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