TY - JOUR
T1 - Single cell transcriptome analysis of human, marmoset and mouse embryos reveals common and divergent features of preimplantation development
AU - Boroviak, Thorsten
AU - Stirparo, Giuliano G.
AU - Dietmann, Sabine
AU - Hernando-Herraez, Irene
AU - Mohammed, Hisham
AU - Reik, Wolf
AU - Smith, Austin
AU - Sasaki, Erika
AU - Nichols, Jennifer
AU - Bertone, Paul
N1 - Funding Information:
This work was supported by grants from the Biotechnology and Biological Sciences Research Council (BBSRC) UK (BB/M004023/1 (RG74277)), by the Medical Research Council (MRC) UK (G1001028), and by funding to the Cambridge Stem Cell Institute from the MRC and Wellcome Trust (097922/Z/11/Z, 203151/Z/16/Z). T.B. is a Wellcome Trust Sir Henry Dale Fellow. A.S. is an MRC Professor. Deposited in PMC for immediate release.
Publisher Copyright:
© 2018. Published by The Company of Biologists Ltd.
PY - 2018
Y1 - 2018
N2 - 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.
AB - 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.
KW - Blastocyst
KW - Embryo
KW - Human
KW - Inner cell mass
KW - Pluripotency
KW - Primate
UR - http://www.scopus.com/inward/record.url?scp=85056417167&partnerID=8YFLogxK
U2 - 10.1242/dev.167833
DO - 10.1242/dev.167833
M3 - Article
C2 - 30413530
AN - SCOPUS:85056417167
SN - 0950-1991
VL - 145
JO - Development (Cambridge)
JF - Development (Cambridge)
IS - 21
M1 - dev167833
ER -