このコンテンツを視聴するには、JoVE 購読が必要です。 サインイン又は無料トライアルを申し込む。
This paper establishes a pipeline for high-quality single-cell and nuclei suspensions of gastrulating mouse embryos for sequencing of single cells and nuclei.
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.
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....
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
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.......
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 .......
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.
....Name | Company | Catalog Number | Comments |
10 cm Petri dish | Genesee Scientific | 25-202 | |
1000 µL Reach Barrier Tip | Genesee Scientific | 23-430 | |
20 µL Reach Barrier Tip | Genesee Scientific | 24-404 | |
300 µL Reach Barrier Tip | Genesee Scientific | 24-415 | |
37 µm Reversible Strainer, small | Stem Cell | 27215 | |
6 cm Petri dish | Genesee Scientific | 25-260 | |
8-strip PCR tubes | Genesee Scientific | 27-125U | |
Agarose | Apex Bioresearch Product | 20-102 | |
Benchmark Scientific BSH300 MyBlock Mini Dry Bath | Genesee | 31-437 | |
Benchmark Scientific Z216-MK Z216MK Hermle Refrigerated Microcentrifuge | Genesee | 33-759R | |
Bovine Serum Albumin (BSA) | Sigma-Aldrich | A2153 | |
Chromium Controller | 10X | PN-1000127 | |
Chromium Next GEM Single Cell 3' Reagent Kits v3.1 | 10X | PN-1000269 | |
Countess 3 Automated Cell Counter | Invitrogen | AMQAX2000 | |
Countess Cell Couning Chamber Slides | Invitrogen | C10283 | |
D1000 Reagents | Agilent | 5067-5583 | |
D1000 ScreenTape | Agilent | 5067-5582 | |
Digitonin | ThermoFisher Scientific | BN2006 | |
DirectPCR yolk sac | Viagen | 201-Y | |
Dithiothreitol (DTT) | ThermoFisher Scientific | R0861 | |
DNA LoBind Tube 1.5 mL | Eppendorf | 22431021 | |
Dubecco's Modificiation of Eagle's Medium (DMEM, 1x) | CORNING | 10-013-CV | |
Dulbecco's PBS | GenClone | 25-508 | |
Dumont #5 Fine Forceps | Fine Science Tools | 11254-20 | |
Dumont #5SF Forceps | Fine Science Tools | 11252-00 | |
Ethanol | Koptec | V1401 | |
EVOS M7000 Imaging System | Invitrogen | AMF7000 | |
Fine Scissors - Sharp | Fine Science Tools | 14060-11 | |
GoTaq G2 Green Master Mix | Promega | M7823 | |
Graefe Forceps | Fine Science Tools | 11049-10 | |
MgCl2 | ThermoFisher Scientific | AC223211000 | |
MiniAmp Thermal Cycler | Applied Biosystems | A37834 | |
NaCl | Fisher Chemical | S271-500 | |
NextSeq 1000/2000 P2 Reagents (100 Cycles) v3 | Illumina | 20046811 | |
NextSeq2000 | Illumina | ||
Nikon SMZ 1000 Stereo Microscope | Nikon | ||
Nondiedt P40 | Sigma-Aldrich | 74385 | |
Nuclease-free Water | GenClone | 25-511 | |
Optical Tube 8x Strip (401428) | Agilent | 401428 | |
Optical Tube Cap 8x Strip (401425) | Agilent | 401425 | |
Poseidon 31-511, HS24 Microcentrifuge, with 24 x 1.5/2.0 mL rotor, 1 Centrifuge/Unit | Genesee | 31-511 | |
Proteinase K | Sigma-Aldrich | P6556 | |
Qubit dsDNA Quantification Assay Kits | Invitrogen | Q32851 | |
Qubit Flex 3 | Invitrogen | ||
RNase inhibitor | Fisher Scientific | 12-141-368 | |
Standard Pattern Forceps | Fine Science Tools | 11000-12 | |
Tape Station Loading tips | Agilent | 5067-5598 | |
Tapestation 4150 | Agilent | G2992AA | |
Tris-HCL (Ph7) | Quality Biological | 351-007-101 | |
Trypan Blue Stain 0.4% | Theromo Fisher Scientific | T10282 | |
Tryple Express | Gibco | 12604-021 | |
Tween-20 | Bio-Rad | 1662404 | |
Vortex mixer IKA MS3 with 96-well sample plate adapter | IKA | 3617000 |
This article has been published
Video Coming Soon
JoVEについて
Copyright © 2023 MyJoVE Corporation. All rights reserved