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Site of the previous meiotic division defines cleavage orientation in the mouse embryo

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/gene.10027openalex-snapshot
Sperm entry position provides a surface marker for the first cleavage plane of the mouse zygote
inferredcites →https://doi.org/10.1002/jez.1401930212openalex-snapshot
A reexamination of cleavage patterns in eutherian mammalian eggs: Rotation of blastomere pairs during second cleavage in the rabbit
inferredcites →https://doi.org/10.1007/s004120050327openalex-snapshot
Mouse polo-like kinase 1 associates with the acentriolar spindle poles, meiotic chromosomes and spindle midzone during oocyte maturation
inferredcites →https://doi.org/10.1016/s0955-0674(01)00292-7openalex-snapshot
Dynein at the cortex
inferredcites →https://doi.org/10.1016/s0960-9822(01)00176-2openalex-snapshot
Nuclear migration: Cortical anchors for cytoplasmic dynein
inferredcites →https://doi.org/10.1016/s0960-9822(07)00516-7openalex-snapshot
Bipolar meiotic spindle formation without chromatin
inferredcites →https://doi.org/10.1016/s0960-9822(98)70208-8openalex-snapshot
Dynein and dynactin are localized to astral microtubules and at cortical sites in mitotic epithelial cells
inferredcites →https://doi.org/10.1016/s0960-9822(98)70465-8openalex-snapshot
The dynactin complex is required for cleavage plane specification in early Caenorhabditis elegans embryos
inferredcites →https://doi.org/10.1038/35054069openalex-snapshot
Role for sperm in spatial patterning of the early mouse embryo
inferredcites →https://doi.org/10.1083/jcb.109.3.1185openalex-snapshot
Centrosome movement in the early divisions of Caenorhabditis elegans: a cortical site determining centrosome position.
inferredcites →https://doi.org/10.1093/humrep/17.9.2368openalex-snapshot
The plane of first cleavage is not related to the distribution of sperm components in the mouse
inferredcites →https://doi.org/10.1093/molehr/3.12.1067openalex-snapshot
Oocyte influences on early development: the regulatory proteins leptin and STAT3 are polarized in mouse and human oocytes and differentially distributed within the cells of the preimplantation stage embryo
inferredcites →https://doi.org/10.1126/science.6857250openalex-snapshot
Nuclear Transplantation in the Mouse Embryo by Microsurgery and Cell Fusion
inferredcites →https://doi.org/10.1242/dev.124.6.1133openalex-snapshot
Following cell fate in the living mouse embryo
inferredcites →https://doi.org/10.1242/dev.125.23.4803openalex-snapshot
Fertile offspring derived from mammalian eggs lacking either animal or vegetal poles
inferredcites →https://doi.org/10.1242/dev.126.24.5591openalex-snapshot
Polarity of the mouse embryo is anticipated before implantation
inferredcites →https://doi.org/10.1242/dev.127.16.3467openalex-snapshot
Animal and vegetal poles of the mouse egg predict the polarity of the embryonic axis, yet are nonessential for development
inferredcites →https://doi.org/10.1242/dev.128.19.3739openalex-snapshot
Blastomeres arising from the first cleavage division have distinguishable fates in normal mouse development
inferredcites →https://doi.org/10.1242/dev.129.4.815openalex-snapshot
Patterning of the embryo: the first spatial decisions in the life of a mouse
inferredcites →https://doi.org/10.1242/dev.48.1.53openalex-snapshot
Features of cell lineage in preimplantation mouse development

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4635259openalex-extracted
Spatial Distribution of Maternal Factors in Pig Mature Oocytes
inferred← citeshttps://doi.org/10.1002/ajmg.a.32741openalex-snapshot
Epidemiology of acephalus/acardius monozygotic twins: New insights into an epigenetic causal hypothesis
inferred← citeshttps://doi.org/10.1002/ajmg.a.35573openalex-snapshot
Assessing pre‐implantation embryo development in mice provides a rationale for understanding potential adverse effects of ART and PGD procedures
inferred← citeshttps://doi.org/10.1002/bdrc.20038openalex-snapshot
The case for prepatterning in the mouse
inferred← citeshttps://doi.org/10.1002/dvg.20377openalex-snapshot
Dynamic rearrangement of surface proteins is essential for cytokinesis
inferred← citeshttps://doi.org/10.1002/jcp.21292openalex-snapshot
Axial specification in mice: Ten years of advances and controversies
inferred← citeshttps://doi.org/10.1007/978-0-387-93877-6_18openalex-snapshot
Actin Doesn’t Do the Locomotion: Secretion Drives Cell Polarization
inferred← citeshttps://doi.org/10.1007/978-0-85729-826-3_18openalex-snapshot
Oocyte Polarity and Its Developmental Significance
inferred← citeshttps://doi.org/10.1007/978-3-642-30406-4_8openalex-snapshot
Preimplantation Mouse Embryo: Developmental Fate and Potency of Blastomeres
inferred← citeshttps://doi.org/10.1007/s00114-003-0490-8openalex-snapshot
Early human development: new data raise important embryological and ethical questions relevant for stem cell research
inferred← citeshttps://doi.org/10.1007/s10815-026-03847-9openalex-snapshot
Alignment among the zygotic cleavage plane, pronuclear axis, and polar axis predicts live birth outcome of blastocyst
inferred← citeshttps://doi.org/10.1007/s12015-016-9648-6openalex-snapshot
The Role of Maternal-Effect Genes in Mammalian Development: Are Mammalian Embryos Really an Exception?
inferred← citeshttps://doi.org/10.1016/b978-0-12-385942-6.00014-7openalex-snapshot
Differentiation in Early Development
inferred← citeshttps://doi.org/10.1016/b978-012436643-5/50021-3openalex-snapshot
Differentiation in Early Development
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50012-9openalex-snapshot
Preimplantation Embryogenesis
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2015.11.006openalex-snapshot
Preformation Versus Epigenesis in Early Mammalian Development
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2016.04.008openalex-snapshot
Polarity in Cell-Fate Acquisition in the Early Mouse Embryo
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2016.05.002openalex-snapshot
Epigenetic Control of Early Mouse Development
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.10.006openalex-snapshot
Maternal factors regulating preimplantation development in mice
inferred← citeshttps://doi.org/10.1016/j.cell.2025.11.006openalex-snapshot
Fertilization triggers early proteomic symmetry breaking in mammalian embryos
inferred← citeshttps://doi.org/10.1016/j.cub.2004.02.031openalex-snapshot
First Cleavage of the Mouse Embryo Responds to Change in Egg Shape at Fertilization
inferred← citeshttps://doi.org/10.1016/j.cub.2004.02.056openalex-snapshot
Embryonic Axes: The Long and Short of It in the Mouse
inferred← citeshttps://doi.org/10.1016/j.cub.2004.02.061openalex-snapshot
Two PAR6 Proteins Become Asymmetrically Localized during Establishment of Polarity in Mouse Oocytes
inferred← citeshttps://doi.org/10.1016/j.cub.2004.12.078openalex-snapshot
Mitotic Spindles and Cleavage Planes Are Oriented Randomly in the Two-Cell Mouse Embryo
inferred← citeshttps://doi.org/10.1016/j.cub.2012.10.054openalex-snapshot
Developmental Bias in Cleavage-Stage Mouse Blastomeres
inferred← citeshttps://doi.org/10.1016/j.devcel.2004.07.012openalex-snapshot
Emerging Asymmetry and Embryonic Patterning in Early Mouse Development
inferred← citeshttps://doi.org/10.1016/j.ejogrb.2004.01.024openalex-snapshot
Ca2+ signalling and cortical re-organisation during the transition from meiosis to mitosis in mammalian oocytes
inferred← citeshttps://doi.org/10.1016/j.gde.2006.06.011openalex-snapshot
The first cell-fate decisions in the mouse embryo: destiny is a matter of both chance and choice
inferred← citeshttps://doi.org/10.1016/j.mam.2013.03.001openalex-snapshot
Quality control of embryo development
inferred← citeshttps://doi.org/10.1016/j.mod.2004.11.014openalex-snapshot
Spatial arrangement of individual 4-cell stage blastomeres and the order in which they are generated correlate with blastocyst pattern in the mouse embryo
inferred← citeshttps://doi.org/10.1016/j.semcdb.2004.04.001openalex-snapshot
The developmental origins of mammalian oocyte polarity
inferred← citeshttps://doi.org/10.1016/j.semcdb.2004.04.002openalex-snapshot
Lineage allocation and cell polarity during mouse embryogenesis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2004.04.004openalex-snapshot
First cell fate decisions and spatial patterning in the early mouse embryo
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.12.033openalex-snapshot
Determination of first cleavage plane: the relationships between the orientation of the mitotic apparatus for first cleavage and the position of meiotic division-related structures in starfish eggs
inferred← citeshttps://doi.org/10.1016/s0012-1606(03)00353-1openalex-snapshot
The evolution of developmental mechanisms
inferred← citeshttps://doi.org/10.1016/s0955-0674(02)00018-2openalex-snapshot
Control of cell polarity and mitotic spindle positioning in animal cells
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60097-1openalex-snapshot
Assisted fertilization and embryonic axis formation in higher primates
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60824-3openalex-snapshot
Cell polarity during folliculogenesis and oogenesis
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)61704-xopenalex-snapshot
Determining the first cleavage of the mouse zygote
inferred← citeshttps://doi.org/10.1016/s1534-5807(03)00404-0openalex-snapshot
A Genome-Wide Study of Gene Activity Reveals Developmental Signaling Pathways in the Preimplantation Mouse Embryo
inferred← citeshttps://doi.org/10.1038/430301aopenalex-snapshot
Plane talk
inferred← citeshttps://doi.org/10.1038/nature02595openalex-snapshot
First cleavage plane of the mouse egg is not predetermined but defined by the topology of the two apposing pronuclei
inferred← citeshttps://doi.org/10.1038/nature03388openalex-snapshot
The first cleavage of the mouse zygote predicts the blastocyst axis
inferred← citeshttps://doi.org/10.1038/nrg1808openalex-snapshot
Roadmap to embryo implantation: clues from mouse models
inferred← citeshttps://doi.org/10.1038/nrm1782openalex-snapshot
Cleavage pattern and emerging asymmetry of the mouse embryo
inferred← citeshttps://doi.org/10.1038/s41467-018-04155-2openalex-snapshot
Tracing the origin of heterogeneity and symmetry breaking in the early mammalian embryo
inferred← citeshttps://doi.org/10.1038/s41467-024-50732-zopenalex-snapshot
Zygotic spindle orientation defines cleavage pattern and nuclear status of human embryos
inferred← citeshttps://doi.org/10.1038/s41598-018-27892-2openalex-snapshot
Double Strand Break DNA Repair occurs via Non-Homologous End-Joining in Mouse MII Oocytes
inferred← citeshttps://doi.org/10.1038/s41598-019-51815-4openalex-snapshot
Fertilization and Cleavage Axes Differ In Primates Conceived By Conventional (IVF) Versus Intracytoplasmic Sperm Injection (ICSI)
inferred← citeshttps://doi.org/10.1080/10495398.2024.2394692openalex-snapshot
Spatial distribution of maternal factors in pig mature oocytes
inferred← citeshttps://doi.org/10.1093/humrep/dei318openalex-snapshot
An investigation of the origin and significance of bilateral symmetry of the pronuclear zygote in the mouse
inferred← citeshttps://doi.org/10.1093/molehr/gaae045openalex-snapshot
Animal and vegetal materials of mouse oocytes segregate at first zygotic cleavage: a simple mechanism that makes the two-cell blastomeres differ reciprocally from the start
inferred← citeshttps://doi.org/10.1093/molehr/gav068openalex-snapshot
Polarity and cell division orientation in the cleavage embryo: from worm to human
inferred← citeshttps://doi.org/10.1098/rstb.2003.1322openalex-snapshot
The basis and significance of pre–patterning in mammals
inferred← citeshttps://doi.org/10.1101/2023.12.30.572752openalex-snapshot
First cleavage is a manifestation of the geometry of the unfertilized oocyte: implications for monozygotic twinning in mice
inferred← citeshttps://doi.org/10.1101/gad.486108openalex-snapshot
Role of Cdx2 and cell polarity in cell allocation and specification of trophectoderm and inner cell mass in the mouse embryo
inferred← citeshttps://doi.org/10.1136/jmg.2009.070466openalex-snapshot
Can our understanding of epigenetics assist with primary prevention of congenital defects?
inferred← citeshttps://doi.org/10.1146/annurev.cellbio.042308.113348openalex-snapshot
From Mouse Egg to Mouse Embryo: Polarities, Axes, and Tissues
inferred← citeshttps://doi.org/10.1242/dev.00170openalex-snapshot
Early patterning of the mouse embryo — contributions of sperm and egg
inferred← citeshttps://doi.org/10.1242/jcs.01666openalex-snapshot
Downregulation of Par3 and aPKC function directs cells towards the ICM in the preimplantation mouse embryo
inferred← citeshttps://doi.org/10.1242/jcs.02873openalex-snapshot
The aPKC–PAR-6–PAR-3 cell polarity complex localizes to the centrosome attracting body, a macroscopic cortical structure responsible for asymmetric divisions in the early ascidian embryo
inferred← citeshttps://doi.org/10.1371/journal.pone.0001241openalex-snapshot
Subcellular Distribution of Mitochondrial Ribosomal RNA in the Mouse Oocyte and Zygote
inferred← citeshttps://doi.org/10.1387/ijdb.062181dgopenalex-snapshot
Unfair debate
inferred← citeshttps://doi.org/10.1387/ijdb.062181jkopenalex-snapshot
Science is not a democracy
inferred← citeshttps://doi.org/10.1387/ijdb.062181thopenalex-snapshot
Where do we stand now? mouse early embryo patterning meeting in Freiburg, Germany (2005)
inferred← citeshttps://doi.org/10.1530/rep.1.00651openalex-snapshot
PAR-1 and the microtubule-associated proteins CLASP2 and dynactin-p50 have specific localisation on mouse meiotic and first mitotic spindles
inferred← citeshttps://doi.org/10.1530/rep.1.00847openalex-snapshot
Regulation of dynamic events by microfilaments during oocyte maturation and fertilization
inferred← citeshttps://doi.org/10.17912/micropub.biology.001181openalex-snapshot
Blastomere size in the human 2-cell embryo predicts the division order that leads to imbalanced lineage contribution to the future body
inferred← citeshttps://doi.org/10.21203/rs.3.rs-7936004/v1openalex-snapshot
Alignment among the zygotic cleavage plane, pronuclear axis, and polar axis predicts live birth outcome of blastocyst
inferred← citeshttps://doi.org/10.4161/cc.4.5.1680openalex-snapshot
Mechanism of First Cleavage Specification in the Mouse Egg: Is Our Body Plan Set at Day 0?
inferred← citeshttps://doi.org/10.7150/ijbs.1.51openalex-snapshot
The GAPs, GEFs, and GDIs of heterotrimeric G-protein alpha subunits
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