Heterogeneity of Mesp1+mesoderm revealed by single-cell RNA-seq

被引:13
作者
Chan, Sunny Sun-Kin [1 ,2 ,3 ]
Chan, Howe H. W. [1 ]
Kyba, Michael [1 ,2 ]
机构
[1] Univ Minnesota, Lillehei Heart Inst, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Canc & Cardiovasc Res Bldg 4-127,2231 6th St SE, Minneapolis, MN 55455 USA
关键词
Mesp1; Mesoderm patterning; Cardiac development; Hematopoiesis; Single-cell RNA-seq; CARDIOVASCULAR PROGENITOR SPECIFICATION; NASCENT MESODERMAL CELLS; CLONAL ANALYSIS REVEALS; EMBRYONIC STEM; MYOGENIC PROGENITORS; GENETIC PROGRAMS; COMMON ORIGIN; MESP1; DIFFERENTIATION; HEAD;
D O I
10.1016/j.bbrc.2016.04.139
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
Mesp1 is a transcription factor that promotes differentiation of pluripotent cells into different mesoderm lineages including hematopoietic, cardiac and skeletal myogenic. This occurs via at least two transient cell populations: a common hematopoietic/cardiac progenitor population and a common cardiac/skeletal myogenic progenitor population. It is not established whether Mesp1-induced mesoderm cells are intrinsically heterogeneous, or are simply capable of multiple lineage decisions. In the current study, we applied single-cell RNA-seq to analyze Mespl+ mesoderm. Initial whole transcriptome analysis showed a surprising homogeneity among Mesp1-induced mesoderm cells. However, this apparent global homogeneity masked an intrinsic heterogeneity revealed by interrogating a panel of early mesoderm patterning factors. This approach enabled discovery of subpopulations primed for hematopoietic or cardiac development. These studies demonstrate the heterogeneic nature of Mesp1+ mesoderm. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:469 / 475
页数:7
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