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A Single-Cell Roadmap of Lineage Bifurcation in Human ESC Models of Embryonic Brain Development

Authors :
Yao, Zizhen
Mich, John K.
Ku, Sherman
Menon, Vilas
Krostag, Anne-Rachel
Martinez, Refugio A.
Furchtgott, Leon
Mulholland, Heather
Bort, Susan
Fuqua, Margaret A.
Gregor, Ben W.
Hodge, Rebecca D.
Jayabalu, Anu
May, Ryan C.
Melton, Samuel
Nelson, Angelique M.
Ngo, N. Kiet
Shapovalova, Nadiya V.
Shehata, Soraya I.
Smith, Michael W.
Tait, Leah J.
Thompson, Carol L.
Thomsen, Elliot R.
Ye, Chaoyang
Glass, Ian A.
Kaykas, Ajamete
Yao, Shuyuan
Phillips, John W.
Grimley, Joshua S.
Levi, Boaz P.
Wang, Yanling
Ramanathan, Sharad
Source :
Cell Stem Cell; January 2017, Vol. 20 Issue: 1 p120-134, 15p
Publication Year :
2017

Abstract

During human brain development, multiple signaling pathways generate diverse cell types with varied regional identities. Here, we integrate single-cell RNA sequencing and clonal analyses to reveal lineage trees and molecular signals underlying early forebrain and mid/hindbrain cell differentiation from human embryonic stem cells (hESCs). Clustering single-cell transcriptomic data identified 41 distinct populations of progenitor, neuronal, and non-neural cells across our differentiation time course. Comparisons with primary mouse and human gene expression data demonstrated rostral and caudal progenitor and neuronal identities from early brain development. Bayesian analyses inferred a unified cell-type lineage tree that bifurcates between cortical and mid/hindbrain cell types. Two methods of clonal analyses confirmed these findings and further revealed the importance of Wnt/β-catenin signaling in controlling this lineage decision. Together, these findings provide a rich transcriptome-based lineage map for studying human brain development and modeling developmental disorders.

Details

Language :
English
ISSN :
19345909
Volume :
20
Issue :
1
Database :
Supplemental Index
Journal :
Cell Stem Cell
Publication Type :
Periodical
Accession number :
ejs40972547
Full Text :
https://doi.org/10.1016/j.stem.2016.09.011