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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This paper establishes a pipeline for high-quality single-cell and nuclei suspensions of gastrulating mouse embryos for sequencing of single cells and nuclei.

Abstract

Over the last decade, single-cell approaches have become the gold standard for studying gene expression dynamics, cell heterogeneity, and cell states within samples. Before single-cell advances, the feasibility of capturing the dynamic cellular landscape and rapid cell transitions during early development was limited. In this paper, a robust pipeline was designed to perform single-cell and nuclei analysis on mouse embryos from embryonic day E6.5 to E8, corresponding to the onset and completion of gastrulation. Gastrulation is a fundamental process during development that establishes the three germinal layers: mesoderm, ectoderm, and endoderm, which are essential for organogenesis. Extensive literature is available on single-cell omics applied to wild-type perigastrulating embryos. However, single-cell analysis of mutant embryos is still scarce and often limited to FACS-sorted populations. This is partially due to the technical constraints associated with the need for genotyping, timed pregnancies, the count of embryos with desired genotypes per pregnancy, and the number of cells per embryo at these stages. Here, a methodology is presented designed to overcome these limitations. This method establishes breeding and timed pregnancy guidelines to achieve a higher chance of synchronized pregnancies with desired genotypes. Optimization steps in the embryo isolation process coupled with a same-day genotyping protocol (3 h) allow for microdroplet-based single-cell to be performed on the same day, ensuring the high viability of cells and robust results. This method further includes guidelines for optimal nuclei isolations from embryos. Thus, these approaches increase the feasibility of single-cell approaches of mutant embryos at the gastrulation stage. We anticipate that this method will facilitate the analysis of how mutations shape the cellular landscape of the gastrula.

Introduction

Gastrulation is a fundamental process required for normal development. This rapid and dynamic process occurs when pluripotent cells transition into lineage-specific precursors that define how organs form. For years, gastrulation was long defined as the formation of three largely homogeneous populations: mesoderm, ectoderm, and endoderm. However, high-resolution technologies and an emerging number of embryonic stem cell models1,2 unveil unprecedented heterogeneity among the early germ layers3,4. This suggests that much more remains to be uncovered about....

Protocol

This protocol and all animal experiments described were formally approved and in accordance with institutional guidelines established by the Temple University Institutional Animal Care and Use Committee, which follows the Association for Assessment and Accreditation of Laboratory Animal Care international guidelines. All mice described were on the C57/BL6N background strain. No animal health concerns were observed in these studies.

1. Breeding colony and timed pregnancies

Representative Results

The methodology designed in this paper is specifically intended to enhance the preparation of embryo samples for single-cell omics from E6.5 to E8. This robust pipeline consists of five major steps: synchronized timed pregnancies, embryo isolations, same-day genotyping, cell dissociation, and assessment of cell viability (Figure 1A). While the presented data focuses on time points from E7 to E7.5, it can be applied to embryos up to E8 (Figure 1B) with small.......

Discussion

A robust pipeline is presented in this paper for obtaining high-quality single-cell and nuclei suspensions from gastrulating mouse embryos, specifically designed to facilitate studies on mechanisms of cell-fate specification in early development. This method addresses a crucial gap in the field of gastrulation by optimizing the analysis of embryos requiring genotypes, such as sex or somatic genes. By utilizing genetic mutation mouse models and employing high-resolution single-cell sequencing on whole mouse embryos, this .......

Acknowledgements

We acknowledge the Genomics Core at the Fox Chase Cancer Center and Dr. Johnathan Whetstine laboratory members Zach Gray, Madison Honer, and Benjamin Ferman for technical support for the sequencing experiments. We acknowledge laboratory members of Dr. Estaras and Alex Morris, a rotation graduate student who contributed to the initial analysis of the single-cell studies. This work is funded by the NIH grants R01HD106969 and R56HL163146 to Conchi Estaras. Additionally, Elizabeth Abraham was supported by T32 training grant 5T32HL091804-12.

....

Materials

NameCompanyCatalog NumberComments
10 cm Petri dishGenesee Scientific25-202
1000 µL Reach Barrier TipGenesee Scientific23-430
20 µL Reach Barrier TipGenesee Scientific24-404
300 µL Reach Barrier TipGenesee Scientific24-415
37 µm Reversible Strainer, smallStem Cell27215
6 cm Petri dishGenesee Scientific25-260
8-strip PCR tubesGenesee Scientific27-125U
AgaroseApex Bioresearch Product20-102
Benchmark Scientific BSH300 MyBlock Mini Dry BathGenesee31-437
Benchmark Scientific Z216-MK Z216MK Hermle Refrigerated MicrocentrifugeGenesee33-759R
Bovine Serum Albumin (BSA)Sigma-AldrichA2153
Chromium Controller10XPN-1000127
Chromium Next GEM Single Cell 3' Reagent Kits v3.110XPN-1000269
Countess 3 Automated Cell CounterInvitrogenAMQAX2000
Countess Cell Couning Chamber SlidesInvitrogenC10283
D1000 ReagentsAgilent5067-5583
D1000 ScreenTapeAgilent5067-5582
DigitoninThermoFisher ScientificBN2006
DirectPCR yolk sacViagen201-Y
Dithiothreitol (DTT)ThermoFisher ScientificR0861
DNA LoBind Tube 1.5 mLEppendorf22431021
Dubecco's Modificiation of Eagle's Medium (DMEM, 1x)CORNING10-013-CV
Dulbecco's PBSGenClone25-508
Dumont #5 Fine ForcepsFine Science Tools11254-20
Dumont #5SF ForcepsFine Science Tools11252-00
EthanolKoptecV1401
EVOS M7000 Imaging SystemInvitrogenAMF7000
Fine Scissors - SharpFine Science Tools14060-11
GoTaq G2 Green Master MixPromegaM7823
Graefe ForcepsFine Science Tools11049-10
MgCl2ThermoFisher ScientificAC223211000
MiniAmp Thermal CyclerApplied BiosystemsA37834
NaClFisher ChemicalS271-500
NextSeq 1000/2000 P2 Reagents (100 Cycles) v3Illumina20046811
NextSeq2000Illumina
Nikon SMZ 1000 Stereo MicroscopeNikon
Nondiedt P40Sigma-Aldrich74385
Nuclease-free WaterGenClone25-511
Optical Tube 8x Strip (401428)Agilent401428
Optical Tube Cap 8x Strip (401425)Agilent401425
Poseidon 31-511, HS24 Microcentrifuge, with 24 x 1.5/2.0 mL rotor, 1 Centrifuge/UnitGenesee31-511
Proteinase KSigma-AldrichP6556
Qubit dsDNA Quantification Assay KitsInvitrogenQ32851
Qubit Flex 3Invitrogen
RNase inhibitorFisher Scientific12-141-368
Standard Pattern ForcepsFine Science Tools11000-12
Tape Station Loading tipsAgilent5067-5598
Tapestation 4150AgilentG2992AA
Tris-HCL (Ph7)Quality Biological351-007-101
Trypan Blue Stain 0.4%Theromo Fisher ScientificT10282
Tryple ExpressGibco12604-021
Tween-20Bio-Rad1662404
Vortex mixer IKA MS3 with 96-well sample plate adapterIKA3617000

References

  1. Arias, A. M., Marikawa, Y., Moris, N. Gastruloids: Pluripotent stem cell models of mammalian gastrulation and embryo engineering. Dev Biol. 488, 35-46 (2022).
  2. Kim, Y., Kim, I., Shin, K.

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