Bovine lineage specification revealed by single-cell gene expression analysis from zygote to blastocyst†

Abstract Preimplantation embryos undergo zygotic genome activation and lineage specification resulting in three distinct cell types in the late blastocyst. The molecular mechanisms underlying this progress are largely unknown in bovines. Here, we sought to analyze an extensive set of regulators at the single-cell level to define the events involved in the development of the bovine blastocyst. Using a quantitative microfluidics approach in single cells, we analyzed mRNA levels of 96 genes known to function in early embryonic development and maintenance of stem cell pluripotency in parallel in 384 individual cells from bovine preimplantation embryos. The developmental transitions can be distinguished by distinctive gene expression profiles and we identified NOTCH1, expressed in early developmental stages, while T-box 3 (TBX3) and fibroblast growth factor receptor 4 (FGFR4), expressed in late developmental stages. Three lineages can be segregated in bovine expanded blastocysts based on the expression patterns of lineage-specific genes such as disabled homolog 2 (DAB2), caudal type homeobox 2 (CDX2), ATPase H+/K+ transporting non-gastric alpha2 subunit (ATP12A), keratin 8 (KRT8), and transcription factor AP-2 alpha (TFAP2A) for trophectoderm; GATA binding protein 6 (GATA6) and goosecoid homeobox (GSC) for primitive endoderm; and Nanog homeobox (NANOG), teratocarcinoma-derived growth factor 1 (TDGF1), and PR/SET domain 14 (PRDM14) for epiblast. Moreover, some lineage-specific genes were coexpressed in blastomeres from the morula. The commitment to trophectoderm and inner cellmass lineages in bovines occurs later than in the mouse, and KRT8 might be an earlier marker for bovine trophectoderm cells. We determined that TDGF1 and PRDM14 might play pivotal roles in the primitive endoderm and epiblast specification of bovine blastocysts. Our results shed light on early cell fate determination in bovine preimplantation embryos and offer theoretical support for deriving bovine embryonic stem cells. Summary Sentence Gene expression analysis of single blastomeres from zygote to blastocyst sheds light on the early cell fate determination in bovine preimplantation embryos and offers theoretical support for deriving bovine embryonic stem cells.

[1]  George Q. Daley,et al.  Derivation of embryonic germ cells and male gametes from embryonic stem cells , 2004, Nature.

[2]  J. Thomson,et al.  Isolation of a primate embryonic stem cell line. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[3]  A. Sharov,et al.  Dynamics of global gene expression changes during mouse preimplantation development. , 2004, Developmental cell.

[4]  H. Van de Velde,et al.  The roles of FGF and MAP kinase signaling in the segregation of the epiblast and hypoblast cell lineages in bovine and human embryos , 2012, Development.

[5]  P. Padilla-Longoria,et al.  Single-cell profiling of epigenetic modifiers identifies PRDM14 as an inducer of cell fate in the mammalian embryo. , 2013, Cell reports.

[6]  Janet Rossant,et al.  Interaction between Oct3/4 and Cdx2 Determines Trophectoderm Differentiation , 2005, Cell.

[7]  P. Pfeffer,et al.  Trophectoderm lineage determination in cattle. , 2011, Developmental cell.

[8]  P. Pfeffer,et al.  Embryo loss in cattle between Days 7 and 16 of pregnancy. , 2010, Theriogenology.

[9]  Craig Obergfell,et al.  Transcriptional profiles of bovine in vivo pre-implantation development , 2014, BMC Genomics.

[10]  杉本 敏美,et al.  Esrrb is a pivotal target of the Gsk3/Tcf3 axis regulating embryonic stem cell self-renewal , 2012 .

[11]  K. Shirahige,et al.  PRDM14 ensures naive pluripotency through dual regulation of signaling and epigenetic pathways in mouse embryonic stem cells. , 2013, Cell stem cell.

[12]  C. Schubert Demethylating the Male Brain , 2015 .

[13]  Mikael Huss,et al.  Resolution of cell fate decisions revealed by single-cell gene expression analysis from zygote to blastocyst. , 2010, Developmental cell.

[14]  M. Goissis,et al.  Functional characterization of CDX2 during bovine preimplantation development in vitro , 2014, Molecular reproduction and development.

[15]  A. Wynshaw-Boris,et al.  Cripto is required for correct orientation of the anterior–posterior axis in the mouse embryo , 1998, Nature.

[16]  K. Betteridge,et al.  Cellular composition and viability of demi- and quarter-embryos made from bisected bovine morulae and blastocysts produced in vitro. , 1998, Theriogenology.

[17]  Kenta Nakai,et al.  Global gene expression of the inner cell mass and trophectoderm of the bovine blastocyst , 2012, BMC Developmental Biology.

[18]  Xiaoan Ruan,et al.  Specific gene-regulation networks during the pre-implantation development of the pig embryo as revealed by deep sequencing , 2014, BMC Genomics.

[19]  Masashi Takahashi,et al.  Transcriptional Wiring for Establishing Cell Lineage Specification at the Blastocyst Stage in Cattle1 , 2013, Biology of reproduction.

[20]  T. Williams,et al.  Pregnancy rates with bisected bovine embryos. , 1984, Theriogenology.

[21]  A. Kruif,et al.  Timing of compaction and inner cell allocation in bovine embryos produced in vivo after superovulation. , 1997, Biology of reproduction.

[22]  M. Kaufman,et al.  Establishment in culture of pluripotential cells from mouse embryos , 1981, Nature.

[23]  Guoji Guo,et al.  BMP signalling regulates the pre-implantation development of extra-embryonic cell lineages in the mouse embryo , 2014, Nature Communications.

[24]  L. Blomberg,et al.  Challenges and prospects for the establishment of embryonic stem cell lines of domesticated ungulates. , 2007, Animal reproduction science.

[25]  M. Biffoni,et al.  Cripto is essential to capture mouse epiblast stem cell and human embryonic stem cell pluripotency , 2016, Nature Communications.

[26]  H. Schöler,et al.  Derivation of Oocytes from Mouse Embryonic Stem Cells , 2003, Science.

[27]  Fabian J Theis,et al.  Characterization of transcriptional networks in blood stem and progenitor cells using high-throughput single-cell gene expression analysis , 2013, Nature Cell Biology.

[28]  Xi Yang,et al.  Establishment of bovine embryonic stem cells after knockdown of CDX2 , 2016, Scientific Reports.

[29]  K. Sugasawa,et al.  PRDM14 promotes active DNA demethylation through the Ten-eleven translocation (TET)-mediated base excision repair pathway in embryonic stem cells , 2014, Development.

[30]  D. Reinberg,et al.  The Polycomb complex PRC2 and its mark in life , 2011, Nature.

[31]  D. Salomon,et al.  The multifaceted role of the embryonic gene Cripto-1 in cancer, stem cells and epithelial-mesenchymal transition. , 2014, Seminars in cancer biology.

[32]  Guoji Guo,et al.  Role of Cdx2 and cell polarity in cell allocation and specification of trophectoderm and inner cell mass in the mouse embryo. , 2008, Genes & development.

[33]  Peter Braude,et al.  Human gene expression first occurs between the four- and eight-cell stages of preimplantation development , 1988, Nature.

[34]  P. Hansen,et al.  Canonical WNT signaling regulates development of bovine embryos to the blastocyst stage , 2011, Scientific Reports.

[35]  Jonathan Göke,et al.  A PRC2‐Dependent Repressive Role of PRDM14 in Human Embryonic Stem Cells and Induced Pluripotent Stem Cell Reprogramming , 2013, Stem cells.

[36]  Takashi Hiiragi,et al.  Stochastic patterning in the mouse pre-implantation embryo , 2007, Development.

[37]  R. Jaenisch,et al.  Generation of nuclear transfer-derived pluripotent ES cells from cloned Cdx2-deficient blastocysts , 2006, Nature.

[38]  L. Blomberg,et al.  Twenty years of embryonic stem cell research in farm animals. , 2012, Reproduction in domestic animals = Zuchthygiene.

[39]  H. Schöler,et al.  Expression Pattern of Oct-4 in Preimplantation Embryos of Different Species , 2000, Biology of reproduction.

[40]  C. Mummery,et al.  Molecular cloning, genetic mapping, and developmental expression of bovine POU5F1. , 1999, Biology of reproduction.

[41]  M. Araúzo-Bravo,et al.  Efficient derivation of pluripotent stem cells from siRNA-mediated Cdx2-deficient mouse embryos. , 2011, Stem cells and development.

[42]  J. Thomson,et al.  Embryonic stem cell lines derived from human blastocysts. , 1998, Science.

[43]  H. Zhang,et al.  Inactivation of nuclear Wnt-β-catenin signaling limits blastocyst competency for implantation , 2008, Development.

[44]  B. N. Day,et al.  The transition from maternal to zygotic control of development occurs during the 4-cell stage in the domestic pig, Sus scrofa: quantitative and qualitative aspects of protein synthesis. , 1991, Biology of reproduction.

[45]  G. Vajta,et al.  Post-hatching development of the porcine and bovine embryo--defining criteria for expected development in vivo and in vitro. , 2006, Theriogenology.

[46]  H. Henderson,et al.  Signal Inhibition Reveals JAK/STAT3 Pathway as Critical for Bovine Inner Cell Mass Development1 , 2015, Biology of reproduction.

[47]  J. Renard,et al.  Molecular evidence for a critical period in mural trophoblast development in bovine blastocysts. , 2005, Developmental biology.

[48]  R. Schultz,et al.  The molecular foundations of the maternal to zygotic transition in the preimplantation embryo. , 2002, Human reproduction update.

[49]  W. A. Kuesa,et al.  Correction for Kues et al., Genome-wide expression profiling reveals distinct clusters of transcriptional regulation during bovine preimplantation development in vivo , 2009, Proceedings of the National Academy of Sciences.

[50]  Austin G Smith,et al.  Capture of Authentic Embryonic Stem Cells from Rat Blastocysts , 2008, Cell.

[51]  H. Hao,et al.  Transcriptome analyses of inner cell mass and trophectoderm cells isolated by magnetic-activated cell sorting from bovine blastocysts using single cell RNA-seq. , 2016, Reproduction in domestic animals = Zuchthygiene.

[52]  Wang Wei,et al.  Di-n-ブチルフタレートは,マウス卵巣胞状濾胞における細胞周期およびアポトーシス経路に関与する遺伝子の発現を混乱させる , 2013 .

[53]  Sandy L. Klemm,et al.  Single-Cell Expression Analyses during Cellular Reprogramming Reveal an Early Stochastic and a Late Hierarchic Phase , 2012, Cell.