Asymmetric Localization of Cdx2 mRNA during the First Cell-Fate Decision in Early Mouse Development

Summary A longstanding question in mammalian development is whether the divisions that segregate pluripotent progenitor cells for the future embryo from cells that differentiate into extraembryonic structures are asymmetric in cell-fate instructions. The transcription factor Cdx2 plays a key role in the first cell-fate decision. Here, using live-embryo imaging, we show that localization of Cdx2 transcripts becomes asymmetric during development, preceding cell lineage segregation. Cdx2 transcripts preferentially localize apically at the late eight-cell stage and become inherited asymmetrically during divisions that set apart pluripotent and differentiating cells. Asymmetric localization depends on a cis element within the coding region of Cdx2 and requires cell polarization as well as intact microtubule and actin cytoskeletons. Failure to enrich Cdx2 transcripts apically results in a significant decrease in the number of pluripotent cells. We discuss how the asymmetric localization and segregation of Cdx2 transcripts could contribute to multiple mechanisms that establish different cell fates in the mouse embryo.

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

[2]  Samantha A. Morris,et al.  Origin and formation of the first two distinct cell types of the inner cell mass in the mouse embryo , 2010, Proceedings of the National Academy of Sciences.

[3]  C. Holt,et al.  Subcellular mRNA Localization in Animal Cells and Why It Matters , 2009, Science.

[4]  Alexander W. Bruce,et al.  Developmental control of the early mammalian embryo: competition among heterogeneous cells that biases cell fate. , 2010, Current opinion in genetics & development.

[5]  J. Dean,et al.  A subcortical maternal complex essential for preimplantation mouse embryogenesis. , 2008, Developmental cell.

[6]  S. Aparício,et al.  Eomesodermin is required for mouse trophoblast development and mesoderm formation , 2000, Nature.

[7]  A. Handyside,et al.  Cell division and death in the mouse blastocyst before implantation , 1986, Roux's archives of developmental biology.

[8]  David Ish-Horowicz,et al.  Conserved signals and machinery for RNA transport in Drosophila oogenesis and embryogenesis , 2001, Nature.

[9]  K. Huth Transport , 2015, Canadian Medical Association Journal.

[10]  Anna-Katerina Hadjantonakis,et al.  Dynamic in vivo imaging and cell tracking using a histone fluorescent protein fusion in mice , 2004, BMC biotechnology.

[11]  H. Krause,et al.  Apical Localization of wingless Transcripts Is Required for Wingless Signaling , 2001, Cell.

[12]  Shinji Yamamoto,et al.  Tead4 is required for specification of trophectoderm in pre-implantation mouse embryos , 2008, Mechanisms of Development.

[13]  Janet Rossant,et al.  Cdx2 acts downstream of cell polarization to cell-autonomously promote trophectoderm fate in the early mouse embryo. , 2008, Developmental biology.

[14]  Janet Rossant,et al.  The Hippo signaling pathway components Lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass. , 2009, Developmental cell.

[15]  C. Ziomek,et al.  The foundation of two distinct cell lineages within the mouse morula , 1981, Cell.

[16]  Ilan Davis,et al.  Transmitting the message: intracellular mRNA localization. , 2010, Current opinion in cell biology.

[17]  H. Schöler,et al.  Oct-4 transcription factor is differentially expressed in the mouse embryo during establishment of the first two extraembryonic cell lineages involved in implantation. , 1994, Developmental biology.

[18]  R. Jansen,et al.  mRNA localization and the cytoskeleton. , 2004, Current opinion in cell biology.

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

[20]  M. DePamphilis,et al.  Transcription factor TEAD4 specifies the trophectoderm lineage at the beginning of mammalian development , 2007, Development.

[21]  Ilan Davis,et al.  RNA localization signals: deciphering the message with bioinformatics. , 2007, Seminars in cell & developmental biology.

[22]  Amber L. Wells,et al.  An Unbiased Analysis Method to Quantify mRNA Localization Reveals Its Correlation with Cell Motility , 2012, Cell reports.

[23]  Janet Rossant,et al.  Cdx 2 acts downstream of cell polarization to cell-autonomously promote trophectoderm fate in the early mouse embryo , 2008 .

[24]  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.

[25]  M. Zernicka-Goetz,et al.  Following cell fate in the living mouse embryo. , 1997, Development.

[26]  Kuniya Abe,et al.  Development and Stem Cells Research Article , 2022 .

[27]  D. Melton Translocation of a localized maternal mRNA to the vegetal pole of Xenopus oocytes , 1987, Nature.

[28]  B. Maro,et al.  The distribution of cytoplasmic actin in mouse 8-cell blastomeres. , 1984, Journal of embryology and experimental morphology.

[29]  T. Schüpbach,et al.  The drosophila dorsoventral patterning gene gurken produces a dorsally localized RNA and encodes a TGFα-like protein , 1993, Cell.

[30]  Nancy Papalopulu,et al.  Downregulation of Par3 and aPKC function directs cells towards the ICM in the preimplantation mouse embryo , 2005, Journal of Cell Science.

[31]  Magdalena Zernicka-Goetz,et al.  Formation of the embryonic-abembryonic axis of the mouse blastocyst: relationships between orientation of early cleavage divisions and pattern of symmetric/asymmetric divisions , 2008, Development.

[32]  M. Murakami,et al.  The Homeoprotein Nanog Is Required for Maintenance of Pluripotency in Mouse Epiblast and ES Cells , 2003, Cell.

[33]  Daniel St Johnston,et al.  Moving messages: the intracellular localization of mRNAs , 2005, Nature Reviews Molecular Cell Biology.

[34]  Alexander W. Bruce,et al.  Maternally and zygotically provided Cdx2 have novel and critical roles for early development of the mouse embryo , 2010, Developmental biology.

[35]  J. Nichols,et al.  Functional Expression Cloning of Nanog, a Pluripotency Sustaining Factor in Embryonic Stem Cells , 2003, Cell.

[36]  J. Derisi,et al.  Cis-acting determinants of asymmetric, cytoplasmic RNA transport. , 2007, RNA.

[37]  Tristan Frum,et al.  Maternal Cdx2 is dispensable for mouse development , 2012, Development.

[38]  Peng Li,et al.  Inscuteable and Staufen Mediate Asymmetric Localization and Segregation of prospero RNA during Drosophila Neuroblast Cell Divisions , 1997, Cell.

[39]  T. Speed,et al.  Inner cell allocation in the mouse morula: the role of oriented division during fourth cleavage. , 1990, Developmental Biology.

[40]  Tony Pawson,et al.  Early lineage segregation between epiblast and primitive endoderm in mouse blastocysts through the Grb2-MAPK pathway. , 2006, Developmental cell.

[41]  Y. Yamanaka Response: Cell fate in the early mouse embryo--sorting out the influence of developmental history on lineage choice. , 2011, Reproductive biomedicine online.

[42]  Michael Zuker,et al.  Mfold web server for nucleic acid folding and hybridization prediction , 2003, Nucleic Acids Res..

[43]  Samantha A. Morris Cell fate in the early mouse embryo: sorting out the influence of developmental history on lineage choice. , 2011, Reproductive biomedicine online.

[44]  R. Lovell-Badge,et al.  Multipotent cell lineages in early mouse development depend on SOX2 function. , 2003, Genes & development.

[45]  Janet Rossant,et al.  Cdx2 is required for correct cell fate specification and differentiation of trophectoderm in the mouse blastocyst , 2005, Development.

[46]  J. Sabina,et al.  Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. , 1999, Journal of molecular biology.