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Single cell transcriptome analysis of human, marmoset and mouse embryos reveals common and divergent features of preimplantation development.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Stirparo, Giuliano G 
Dietmann, Sabine 
Hernando-Herraez, Irene 
Mohammed, Hisham 

Abstract

The mouse embryo is the canonical model for mammalian preimplantation development. Recent advances in single cell profiling allow detailed analysis of embryogenesis in other eutherian species, including human, to distinguish conserved from divergent regulatory programs and signalling pathways in the rodent paradigm. Here, we identify and compare transcriptional features of human, marmoset and mouse embryos by single cell RNA-seq. Zygotic genome activation correlates with the presence of polycomb repressive complexes in all three species, while ribosome biogenesis emerges as a predominant attribute in primate embryos, supporting prolonged translation of maternally deposited RNAs. We find that transposable element expression signatures are species, stage and lineage specific. The pluripotency network in the primate epiblast lacks certain regulators that are operative in mouse, but encompasses WNT components and genes associated with trophoblast specification. Sequential activation of GATA6, SOX17 and GATA4 markers of primitive endoderm identity is conserved in primates. Unexpectedly, OTX2 is also associated with primitive endoderm specification in human and non-human primate blastocysts. Our cross-species analysis demarcates both conserved and primate-specific features of preimplantation development, and underscores the molecular adaptability of early mammalian embryogenesis.

Description

Keywords

Blastocyst, Embryo, Human, Inner cell mass, Pluripotency, Primate, Animals, Callithrix, Conserved Sequence, Embryo, Mammalian, Embryonic Development, Endoderm, Epigenesis, Genetic, Gene Expression Profiling, Gene Expression Regulation, Developmental, Gene Regulatory Networks, Germ Layers, Humans, Mice, Otx Transcription Factors, RNA, Messenger, Ribosomes, Single-Cell Analysis, Transcription, Genetic, Transcriptome

Journal Title

Development

Conference Name

Journal ISSN

0950-1991
1477-9129

Volume Title

145

Publisher

The Company of Biologists
Sponsorship
Biotechnology and Biological Sciences Research Council (BB/M004023/1)
Wellcome Trust (097922/Z/11/Z)
Medical Research Council (G1001028)
Medical Research Council (MR/P00072X/1)
Wellcome Trust (203151/Z/16/Z)
This work was supported by grants from the Biotechnology and Biological Sciences Research Council (BBSRC) UK (BB/M004023/1 (RG74277)), the Medical Research Council (MRC) UK (G1001028), and funding to the Cambridge Stem Cell Institute from the MRC and Wellcome Trust (097922/Z/11/Z, 203151/Z/16/Z). TB is a Wellcome Trust Sir Henry Dale Fellow. AS is an MRC Professor
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