Dynamics of lineage commitment revealed by single-cell transcriptomics of differentiating embryonic stem cells

被引:120
作者
Semrau, Stefan [1 ,2 ,3 ,4 ]
Goldmann, Johanna E. [3 ]
Soumillon, Magali [5 ,6 ,7 ]
Mikkelsen, Tarjei S. [5 ,6 ,7 ]
Jaenisch, Rudolf [3 ,8 ]
van Oudenaarden, Alexander [1 ,2 ]
机构
[1] Royal Netherlands Acad Arts & Sci, Hubrecht Inst KNAW, Uppsalalaan 8, NL-3584 CT Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Uppsalalaan 8, NL-3584 CT Utrecht, Netherlands
[3] Whitehead Inst Biomed Res, 9 Cambridge Ctr, Cambridge, MA 02142 USA
[4] Leiden Inst Phys, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
[5] Broad Inst, 415 Main St, Cambridge, MA 02142 USA
[6] Harvard Univ, Harvard Stem Cell Inst, 7 Divin Ave, Cambridge, MA 02138 USA
[7] Harvard Univ, Dept Stem Cell & Regenerat Biol, 7 Divin Ave, Cambridge, MA 02138 USA
[8] MIT, Dept Biol, 31 Ames St, Cambridge, MA 02142 USA
关键词
FATE DECISIONS; PRIMITIVE ENDODERM; GENE-EXPRESSION; GROUND-STATE; SELF-RENEWAL; RNA-SEQ; PLURIPOTENCY FACTORS; NAIVE; CONTRIBUTES; SEGREGATION;
D O I
10.1038/s41467-017-01076-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Gene expression heterogeneity in the pluripotent state of mouse embryonic stem cells (mESCs) has been increasingly well-characterized. In contrast, exit from pluripotency and lineage commitment have not been studied systematically at the single-cell level. Here we measure the gene expression dynamics of retinoic acid driven mESC differentiation from pluripotency to lineage commitment, using an unbiased single-cell transcriptomics approach. We find that the exit from pluripotency marks the start of a lineage transition as well as a transient phase of increased susceptibility to lineage specifying signals. Our study reveals several transcriptional signatures of this phase, including a sharp increase of gene expression variability and sequential expression of two classes of transcriptional regulators. In summary, we provide a comprehensive analysis of the exit from pluripotency and lineage commitment at the single cell level, a potential stepping stone to improved lineage manipulation through timing of differentiation cues.
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页数:16
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