Cell-specific network constructed by single-cell RNA sequencing data

Abstract Single-cell RNA sequencing (scRNA-seq) is able to give an insight into the gene–gene associations or transcriptional networks among cell populations based on the sequencing of a large number of cells. However, traditional network methods are limited to the grouped cells instead of each single cell, and thus the heterogeneity of single cells will be erased. We present a new method to construct a cell-specific network (CSN) for each single cell from scRNA-seq data (i.e. one network for one cell), which transforms the data from ‘unstable’ gene expression form to ‘stable’ gene association form on a single-cell basis. In particular, it is for the first time that we can identify the gene associations/network at a single-cell resolution level. By CSN method, scRNA-seq data can be analyzed for clustering and pseudo-trajectory from network perspective by any existing method, which opens a new way to scRNA-seq data analyses. In addition, CSN is able to find differential gene associations for each single cell, and even ‘dark’ genes that play important roles at the network level but are generally ignored by traditional differential gene expression analyses. In addition, CSN can be applied to construct individual network of each sample bulk RNA-seq data. Experiments on various scRNA-seq datasets validated the effectiveness of CSN in terms of accuracy and robustness.

[1]  Bo Wang,et al.  Visualization and analysis of single-cell RNA-seq data by kernel-based similarity learning , 2016, Nature Methods.

[2]  Wei Vivian Li,et al.  An accurate and robust imputation method scImpute for single-cell RNA-seq data , 2018, Nature Communications.

[3]  A. Murphy,et al.  RNA Sequencing of Single Human Islet Cells Reveals Type 2 Diabetes Genes. , 2016, Cell metabolism.

[4]  G. Cagney,et al.  The variant Polycomb Repressor Complex 1 component PCGF1 interacts with a pluripotency sub-network that includes DPPA4, a regulator of embryogenesis , 2015, Scientific Reports.

[5]  K. Aihara,et al.  Personalized characterization of diseases using sample-specific networks , 2016, bioRxiv.

[6]  Kazuyuki Aihara,et al.  Detection for disease tipping points by landscape dynamic network biomarkers , 2018, National science review.

[7]  Aleksandra A. Kolodziejczyk,et al.  Single Cell RNA-Sequencing of Pluripotent States Unlocks Modular Transcriptional Variation , 2015, Cell stem cell.

[8]  Masamitsu N. Asaka,et al.  Link between embryonic stem cell pluripotency and homologous allelic pairing of Oct4 loci , 2017, Development, growth & differentiation.

[9]  Peter J. Rousseeuw,et al.  Finding Groups in Data: An Introduction to Cluster Analysis , 1990 .

[10]  Junhyong Kim,et al.  The promise of single-cell sequencing , 2013, Nature Methods.

[11]  T. Burdon,et al.  Oct‐4 Knockdown Induces Similar Patterns of Endoderm and Trophoblast Differentiation Markers in Human and Mouse Embryonic Stem Cells , 2004, Stem cells.

[12]  E. Shapiro,et al.  Single-cell sequencing-based technologies will revolutionize whole-organism science , 2013, Nature Reviews Genetics.

[13]  David G. Kirsch,et al.  Application of single-cell RNA sequencing in optimizing a combinatorial therapeutic strategy in metastatic renal cell carcinoma , 2016, Genome Biology.

[14]  S. Teichmann,et al.  Computational and analytical challenges in single-cell transcriptomics , 2015, Nature Reviews Genetics.

[15]  Chen Li,et al.  Dysfunction of PLA2G6 and CYP2C44-associated network signals imminent carcinogenesis from chronic inflammation to hepatocellular carcinoma , 2017, Journal of molecular cell biology.

[16]  R. Stewart,et al.  Single-cell RNA-seq reveals novel regulators of human embryonic stem cell differentiation to definitive endoderm , 2016, Genome Biology.

[17]  Fabian J Theis,et al.  Computational analysis of cell-to-cell heterogeneity in single-cell RNA-sequencing data reveals hidden subpopulations of cells , 2015, Nature Biotechnology.

[18]  Geoffrey E. Hinton,et al.  Visualizing Data using t-SNE , 2008 .

[19]  S. Quake,et al.  A survey of human brain transcriptome diversity at the single cell level , 2015, Proceedings of the National Academy of Sciences.

[20]  Kazuyuki Aihara,et al.  Detecting early-warning signals for sudden deterioration of complex diseases by dynamical network biomarkers , 2012, Scientific Reports.

[21]  Chen Xu,et al.  Identification of cell types from single-cell transcriptomes using a novel clustering method , 2015, Bioinform..

[22]  Sean C. Bendall,et al.  Single-Cell Trajectory Detection Uncovers Progression and Regulatory Coordination in Human B Cell Development , 2014, Cell.

[23]  Martin Sill,et al.  SEURAT: Visual analytics for the integrated analysis of microarray data , 2010, BMC Medical Genomics.

[24]  Kazuyuki Aihara,et al.  Quantifying critical states of complex diseases using single-sample dynamic network biomarkers , 2017, PLoS Comput. Biol..

[25]  I. Amit,et al.  Massively Parallel Single-Cell RNA-Seq for Marker-Free Decomposition of Tissues into Cell Types , 2014, Science.

[26]  M. Schaub,et al.  SC3 - consensus clustering of single-cell RNA-Seq data , 2016, Nature Methods.

[27]  Meiyi Li,et al.  Dynamic network biomarker indicates pulmonary metastasis at the tipping point of hepatocellular carcinoma , 2018, Nature Communications.

[28]  R. Lahesmaa,et al.  The L1TD1 Protein Interactome Reveals the Importance of Post-transcriptional Regulation in Human Pluripotency , 2015, Stem cell reports.

[29]  H. Lehrach,et al.  Analysis of Oct4‐Dependent Transcriptional Networks Regulating Self‐Renewal and Pluripotency in Human Embryonic Stem Cells , 2007, Stem cells.

[30]  S. Linnarsson,et al.  Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq , 2015, Science.

[31]  Kazuyuki Aihara,et al.  Hunt for the tipping point during endocrine resistance process in breast cancer by dynamic network biomarkers , 2018, Journal of molecular cell biology.

[32]  Luonan Chen,et al.  Part mutual information for quantifying direct associations in networks , 2016, Proceedings of the National Academy of Sciences.

[33]  Cole Trapnell,et al.  The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells , 2014, Nature Biotechnology.

[34]  Hans Clevers,et al.  Single-cell messenger RNA sequencing reveals rare intestinal cell types , 2015, Nature.

[35]  Yan Gao,et al.  Identification of Cell Types from Single-Cell Transcriptomes Using a Novel Clustering Framework , 2020, ICIC.

[36]  Alex A. Pollen,et al.  Low-coverage single-cell mRNA sequencing reveals cellular heterogeneity and activated signaling pathways in developing cerebral cortex , 2014, Nature Biotechnology.