Mammalian organogenesis is a remarkable process. Within a short timeframe, the cells of the three germ layers transform into an embryo that includes most of the major internal and external organs. Here we investigate the transcriptional dynamics of mouse organogenesis at single-cell resolution. Using single-cell combinatorial indexing, we profiled the transcriptomes of around 2 million cells derived from 61 embryos staged between 9.5 and 13.5 days of gestation, in a single experiment. The resulting ‘mouse organogenesis cell atlas’ (MOCA) provides a global view of developmental processes during this critical window. We use Monocle 3 to identify hundreds of cell types and 56 trajectories, many of which are detected only because of the depth of cellular coverage, and collectively define thousands of corresponding marker genes. We explore the dynamics of gene expression within cell types and trajectories over time, including focused analyses of the apical ectodermal ridge, limb mesenchyme and skeletal muscle.
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The sci-RNA-seq3 protocol and all data have been made freely available, including through a cell-type wiki to facilitate their ongoing annotation by the research community (http://atlas.gs.washington.edu/mouse-rna). The data generated in this study can be downloaded in raw and processed forms from the NCBI Gene Expression Omnibus under accession number GSE119945.
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We thank members of the Shendure and Trapnell labs, especially D. Cusanovich, R. Daza, G. Findlay, A. McKenna, H. Pliner and V. Ramani, as well as L. McInnes, D. Beier, N. Ahituv and S. Tapscott for helpful discussions and feedback; M. Zager for major contributions to the website; R. Hunter, and R. Rualo at the Transgenic Resources Program of University of Washington and N. Brieske and A. Stiege at the Max Planck Institute for Molecular Genetics for their assistance; S. Geuer for the Fndc3a probe. M.S. was supported by a grant from the Deutsche Forschungsgemeinschaft (SP1532/3-1). This work was funded by the Paul G. Allen Frontiers Group (Allen Discovery Center grant to J.S. and C.T.), grants from the NIH (DP1HG007811 and R01HG006283 to J.S.; DP2 HD088158 to C.T.), the W. M. Keck Foundation (to C.T. and J.S.). J.S. is an Investigator of the Howard Hughes Medical Institute.
Nature thanks Alistair Forrest, Peter Sims, Patrick Tam and the other anonymous reviewer(s) for their contribution to the peer review of this work.
L.C., F.Z. and F.J.S. declare competing financial interests in the form of stock ownership and paid employment by Illumina. One or more embodiments of one or more patents and patent applications filed by Illumina may encompass the methods, reagents and data disclosed in this manuscript. Some work in this study may be related to technology described in the following exemplary published patent applications: WO2010/0120098 and WO2011/0287435.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
Extended Data Fig. 1 Performance and quality-control-related analyses for sci-RNA-seq3.
a, Comparison of fixation conditions in human HEK-293T cells. PFA-fixed nuclei yielded the highest numbers of UMIs. Cell number: n = 21 for fresh nuclei, 17 for frozen nuclei, 32 for PFA-fixed cells and 31 for PFA-fixed nuclei. b, Tn5 transposomes loaded only with N7 adaptor (cell number, n = 13 cells) increased UMI counts by over 50%, relative to the standard Nextera Tn5 (cell number, n = 11), in human HEK-293T cells. c, Bar plot showing the number of reverse transcription wells used for each of 61 mouse embryos. d, Histogram showing the distribution of raw sequencing reads from each PCR well in sci-RNA-seq3. e, Scatter plot of mouse (NIH/3T3) versus human (HEK-293T) UMI counts per cell. f, g, Box plot showing the number of UMIs and purity (proportion of reads mapping to the expected species) per cell from HEK-293T (cell number n = 7,943) and NIH/3T3 cells (cell number, n = 10,914). At a sequencing depth of 23,207 reads per cell, we observed a median of 5,461 UMIs per HEK-293T cell and 5,087 UMIs per NIH/3T3 cell, with 3.9% and 2.9% of reads per cell mapping to incorrect species, respectively. h, Box plot comparing the number of UMIs per cell (downsampled to 20,000 raw reads per cell) for sci-RNA-seq3 (cell number, n = 689 for HEK-293T and 997 for NIH/3T3) versus sci-RNA-seq (cell number, n = 47 for HEK-293T and 120 for NIH/3T3). i, Correlation (Pearson’s correlation) between gene expression measurements in aggregated profiles of HEK-293T from sci-RNA-seq3 nuclei versus sci-RNA-seq cells. j, Scatter plot showing correlation between number of reverse transcription wells used and number of cells recovered per embryo. k, Box plot showing the number of genes and UMIs detected per cell. l, Box plot showing the number of UMIs detected per cell from embryos across five developmental stages. Cell number: n = 152,120 for E9.5; 378,427 for E10.5; 615,908 for E11.5; 475,047 for E12.5; 437,150 for E13.5. m, Histogram showing the distribution of the cell doublet score for the actual mouse embryo data versus doublets stimulated by Scrublet. n, Scatter plot of the number of cells profiled per reverse transcription well and the detected doublet-cell ratio. Blue line shows the linear regression. The detected doublet-cell rate was modestly correlated with number of cells profiled per well during reverse transcription (Spearman’s ρ = 0.35). o, Scatter plot of unique reads aligning to Xist (female-specific) versus chrY transcripts (male-specific) per mouse embryo. Sex assignments of individual embryos inferred from these data. p, Bar plot showing the number of male and female embryos profiled at each developmental stage. q, t-SNE of the aggregated transcriptomes of single cells derived from each of 61 mouse embryos results in 5 tightly clustered groups perfectly matching their developmental stages (embryo number, n = 61). r, Pseudotime trajectory of pseudobulk RNA-seq profiles of mouse embryos (embryo number, n = 61); identical to Fig. 1c, but coloured by pseudotime. s, The E10.5 embryos were ordered by pseudotime. The 3 earliest versus 3 latest (in pseudotime) E10.5 embryos are shown in photographs, and appear to potentially be morphologically distinct. Notably, the distinct colouring of E10.5 embryos positioned earlier versus later in developmental pseudotime is potentially due to different levels of haemoglobin. For all box plots: thick horizontal lines, medians; upper and lower box edges, first and third quartiles, respectively; whiskers, 1.5 times the interquartile range; circles, outliers.
Extended Data Fig. 2 Identifying the major cell types and cell-composition dynamics during mouse organogenesis.
a–e, t-SNE visualization of mouse embryo cells from different developmental stages, with sampling 10,000 cells per stage and colouring by embryo ID: E9.5 (a), E10.5 (b), E11.5 (c), E12.5 (d), E13.5 (e). We consistently observe that cells derived from independent embryos at the same time point are similarly distributed. f, The same t-SNE as Fig. 2a is shown, with subsets of cells highlighted. The first panel only shows cells from E9.5 embryos, and cells from subsequent developmental stages are progressively added. g, Box plot showing the number of UMIs detected per cell for major cell types (cell number n for each cell type is listed in Supplementary Table 3). Thick horizontal lines, medians; upper and lower box edges, first and third quartiles, respectively; whiskers, 1.5 times the interquartile range; circles, outliers. h, t-SNE visualization of a randomly sampled 100,000 cells coloured by expression level of Hbb-bh1 (top) or Fndc3c1 (bottom). ‘High’ indicates cells with UMI count for Hbb-bh1 >3 or Fndc3c1 >1. i, Bar plot showing the number of marker genes in each major cell type, defined as differentially expressed genes (5% FDR) with a >twofold (green) or >fivefold (red) expression difference between first- and second-ranked cell types. j, Left, t-SNE visualization of a randomly sampled 100,000 cells coloured by expression level of Shh (top) or Tox2 (bottom). Right, WISH images of Shh (top) or Tox2 (bottom) in embryos. n = 5. ‘High’ indicates cells with UMI count for Shh> 0 or Tox2 >1. Arrow, site of gene expression. k, Bar plot showing the number of cells profiled for each cell type, split by development stage. l, Heat map showing the estimated relative number of each cell type (rows) in 61 mouse embryos (columns). An estimate of the absolute cell number per cell type per embryo was calculated by multiplying the proportion that cell type contributed to a given embryo by the estimated total number of cells at that development stage. For presentation, these estimates are normalized in each row by the maximum estimated cell count for that cell type across all 61 embryos. Embryos are sorted left-to-right by developmental pseudotime. m, Line plot showing the estimated relative cell numbers for primitive erythroid and definitive erythroid lineages, calculated as in l. Dashed lines show relative expression of marker genes for primitive erythroid (Hbb-bh1) and definitive erythroid (Hbb-bs) major cell types. Data points for individual embryos were ordered by development pseudotime and smoothed by the LOESS method.
Extended Data Fig. 3 Louvain clustering and t-SNE visualization of subclusters of the each of 38 major cell types.
As cell-type heterogeneity was readily apparent within many of the 38 clusters shown in Fig. 2a, we adopted an iterative strategy, repeating Louvain clustering on each main cell type to identify subclusters. After subclusters dominated by 1 or 2 embryos were removed and highly similar subclusters were merged, a total of 655 subclusters were identified. (also termed ‘subtypes’ to distinguish them from the 38 major cell types identified by the initial clustering). Cell number, n, for each cell type is listed in Supplementary Table 3.
Extended Data Fig. 4 Analysis of cell subtypes during mouse organogenesis.
a, t-SNE visualization of all cells (top plot, n = 2,026,641) and downsampled subset of high-quality cells (bottom plot, n = 50,000, UMI > 400), coloured by Louvain cluster IDs from Fig. 2a. b, t-SNE visualization of all endothelial cells (top plot, n = 35,878) and those from the downsampled subset (bottom plot, n = 1,173), coloured by Louvain cluster ID computed on the basis of the 35,878 endothelial cells. c, d, t-SNE visualization of the downsampled subset of 50,000 cells (c), and 1,173 endothelial cells (d), coloured by Louvain cluster ID computed on the basis of sampled cells only. The number of clusters and subclusters identified with the same parameters drops from 38 (a, bottom plot) to 27 (c) and 16 (b, bottom plot) to 12 (c), respectively. e, Histogram showing the distribution of subclusters with respect to cell number (median 1,869; range 51–65,894). f, Histogram showing the distribution of subclusters with respect to the number of contributing embryos (>5 cells to qualify as a contributor). g, Histogram showing the distribution of subclusters with respect to the ratio of cells derived from the most highly contributing embryo. h, Histogram showing the distribution of subclusters with respect to the ratio of doublet cells detected by Scrublet. i, Histogram showing the distribution of subclusters with respect to the number of marker genes (at least twofold (blue)- or fivefold (red)-higher expression when compared with the second-highest expressing cell subtype within the same main cluster; 5% FDR). Out of 655 subclusters, 644 (98%) have at least 1 such gene marker with a twofold difference, and 441 of 655 (67%) have at least 1 such marker with a fivefold difference. j, t-SNE visualization of subcluster-specific marker expression (for example, cell number n = 74,651): Calb1 (left), Nox3 (middle) and Tex14 (right) are gene markers for three endothelial subclusters. ‘High’ indicates cells with UMI count for Calb1 >0, Nox3 >0 or Tex14 >1. k, Cumulative histogram showing how many subtypes (out of a total of 572 non-doublet-artefact subtypes) can be distinguished from all other subtypes on the basis of 1 or several markers and >fourfold expression differences (see also Methods, Supplementary Table 5).
Extended Data Fig. 5 Cell-type correlation analysis between single-cell mouse atlases.
a, Cell-type correlation analysis (Methods) matched cell types between independently generated and annotated analyses of the adult mouse kidney (sci-RNA-seq component of sci-CAR19 (rows) versus Microwell-seq10 (columns)). All cell types identified by sci-RNA-seq are shown, but we only show Microwell-seq cell types that are top matches for one or more sci-RNA-seq cell types. Colours correspond to beta values, normalized by the maximum beta value per row. b, Left, we compared our subtypes against 130 fetal cell types annotated in the MCA10 with cell-type correlation analysis, matching 96 MCA-defined cell types (rows) to 58 subtypes in our mouse embryo atlas (columns). Colours correspond to beta values, normalized by the maximum beta value per row. All MCA cell types with maximum beta of matched cell type >0.01 are shown (rows; n = 96), as are mouse embryo atlas cell types that are top matches for one or more displayed MCA cell types (columns; n = 58). Right, zoom-in of a subset of matches shown on the left. Cell-type annotations are from MCA (rows) or our study (columns; major cell-type annotation and subcluster ID). c, Box plot showing the ratio of cells from E13.5 for subclusters with (subcluster number, n = 58) versus without (subcluster number, n = 514) a matched cell type in the MCA. Thick horizontal lines, medians; upper and lower box edges, first and third quartiles, respectively; whiskers, 1.5 times the interquartile range; circles, outliers. d, Left, we compared our subtypes against 265 cell types annotated by a recent mouse brain cell atlas (BCA)32 with cell-type correlation analysis, matching 48 BCA-defined cell types (rows) to 68 subtypes in our data (columns). Colours correspond to beta values, normalized by the maximum beta value per row. All mouse embryo cell types with maximum beta of matched cell type >0.01 are shown (column; n = 68), as are BCA cell types that are top matches for 1 or more displayed mouse embryo cell types (rows; n = 48). Right, zoom-in of a subset of matches shown on the left. Cell-type annotations are from BCA (rows) or our study (columns; major cell cluster and subcluster ID).
Extended Data Fig. 6 Analysis of mouse epithelium, endothelium and limb-AER cells.
a, b, Dot plot showing expression of one selected marker gene per epithelial (a) or endothelial (b) subtype. Doublet-derived subclusters (2/29 epithelial subtypes and 5/16 endothelial subtypes) are excluded from these plots, but are shown in Fig. 3a and in c, respectively. The size of the dot encodes the percentage of cells within a cell type, and its colour encodes the average expression level. c, t-SNE visualization and marker-based annotation of endothelial cell subtypes (n = 35,878). d, Heat map showing smoothed pseudotime-dependent differential gene expression (510 genes at FDR of 1%) in AER cells, generated by a spline fitting with a generalized linear model (assuming gene expression following the negative binomial distribution) and scaled as a percentage of maximum gene expression. Each row indicates a different gene, and these are split into subsets that are activated (top), repressed (middle) or exhibit transient dynamics (bottom) between E9.5 and E13.5. e, f, Plots showing the −log-transformed q value and Enrichr-based combined score of enriched Reactome terms (e) and transcription factors (f) for genes with expression that significantly decreases in AER development. The top enriched pathway terms (Reactome2016) for significantly decreasing genes include cell-cycle progression (‘mitotic cell cycle’, q = 0.0002, one-sided Fisher exact test with multiple comparisons adjusted) and glucose metabolism (metabolism of carbohydrates, q = 0.0002, one-sided Fisher exact test with multiple comparisons adjusted). The top enriched transcription factors with targets from decreasing genes include pluripotent factors such as Isl1 (q < 1 × 10−5), Pou5f1 (q = 0.002, one-sided Fisher exact test with multiple comparisons adjusted) and Nanog (q = 0.003, one-sided Fisher exact test with multiple comparisons adjusted).
Extended Data Fig. 7 Characterizing cellular trajectories during limb mesenchyme differentiation.
a, UMAP 3D visualization of limb mesenchymal cells coloured by development stage (cell number, n = 26,559; left and right represent views from two directions). b, Heat map showing top differentially expressed genes between different developmental stages for limb mesenchyme cells. c, Bar plot showing the −log10-transformed adjusted P value (one-sided Fisher exact test with multiple comparisons adjusted) of enriched transcription factors for significantly upregulated genes during limb mesenchyme development. d, t-SNE visualization of limb mesenchyme cells coloured by forelimb (Tbx5+; cell number, n = 2,085) and hindlimb (Pitx1+; cell number, n = 1,885). Cells with no expression or expression of both in Tbx5 and Pitx1 are not shown. e, h, i, k, Each panel illustrates a different marker gene. Colours indicate UMI counts that have been scaled for library size, log-transformed, and then mapped to Z-scores to enable comparison between genes. Cells with no expression of a given marker are excluded to prevent overplotting. e, Hindlimb marker Pitx1 and forelimb marker Tbx5. f, Scatter plot showing the normalized expression of Pitx1 and Tbx5 in limb mesenchyme cells. Only cells in which Pitx1 and/or Tbx5 were detected are shown. g, Volcano plot showing the differentially expressed genes (FDR of 5%, one-sided likelihood ratio test with multiple comparisons adjusted, coloured red) between forelimb (cell number, n = 2,085) and hindlimb (cell number, n = 1,885). Top differentially expressed genes are labelled. x axis, log2-transformed fold change between forelimb and hindlimb for each gene; y axis, −log10-transformed q value from differential gene expression test. h, Same visualization as e, coloured by normalized gene expression of proximal/chondrocyte (Sox6 and Sox9), distal (Hoxd13 and Tfap2b), anterior (Pax9 and Alx4) or posterior (Hand2 and Shh) markers. Only cells with the gene marker expressed are plotted. i, Same visualization as e. First row, proximal limb markers Sox6 (which also marks chondrocytes) and Sox9. Second row, distal limb markers Hoxd13 and Tfap2b. Third row, anterior limb markers65 Pax9 and Alx4. Fourth row, posterior limb markers Shh and Hand2. j, In situ hybridization images of Hoxd13 in E9.5 to E13.5 embryos (n = 5). k, Same visualization as e, coloured by normalized gene expression of Cpa2. Only cells with positive UMI counts are shown. Values are log-transformed, standardized UMI counts. The expression pattern of Cpa2 within this trajectory led us to predict that it is a distal marker of the developing limb mesenchyme, similiar to Hoxd13. l, In situ hybridization images of Cpa2 in E10.5 and E11.5 embryos (n = 5. Arrow, site of gene expression. m, Modules of spatially restricted genes in the limbs. A total of 1,783 genes were clustered via hierarchical clustering. The dendrogram was cut into eight modules using the cutree function in R, and the aggregate expression of genes in each module was computed. Colours indicate aggregate UMI counts for each module that have been scaled for library size, log-transformed and then mapped to Z-scores to enable comparison between modules. Cells with no expression of a given module are excluded to prevent overplotting.
Extended Data Fig. 8 Characterization of ten major developmental trajectories present during mouse organogenesis.
a, Heat map showing the proportion of cells from each of the 38 major cell types assigned to each of the 12 PAGA algorithm-identified groups. We merged 2 groups corresponding to sensory neurons (12 and 3) and another 2 groups corresponding to blood cells (6 and 7) as each pair was closely located in UMAP space upon visual inspection, yielding the 10 supergroups shown in a similar heat map in Fig. 4b. b, Same as Fig. 4a, but with colours corresponding to the 38 major cell clusters. c, Area plot showing the estimated proportion (top) and estimated absolute number (bottom) of cells per embryo derived from each of the ten major cell trajectories from E9.5 to E13.5. Although the estimated number of cells per embryo in each of these supergroups increases exponentially, their proportions remain relatively stable, with the exception of hepatocytes which expand their contribution by nearly tenfold during this developmental window (from 0.3% at E9.5 to 2.8% at E13.5). d, UMAP 3D visualization of epithelial subtrajectories (as in Fig. 4c), coloured as per the epithelial subtypes shown in Fig. 3a.
Extended Data Fig. 9 UMAP visualization of the ten major cell trajectories.
We iteratively reanalysed each of the ten major trajectories, nearly all of which further resolved into multiple subtrajectories. The 10 major cell trajectories are visualized with UMAP (as in Fig. 5) but coloured: as per the 38 major cell clusters (top left), subcluster ID (top right), developmental stage (bottom left) and pseudotime (bottom right). The lines correspond to the principal graph learned by Monocle 3. These images are also available at http://atlas.gs.washington.edu/mouse-rna as manipulatable 3D renderings.
Extended Data Fig. 10 UMAP visualization of the 56 subtrajectories, coloured by development stage.
We further iteratively reanalysed and visualized with UMAP each of the 56 subtrajectories. Although Monocle 3 did not have access to these labels, the subtrajectories are highly consistent with developmental time (that is, cells ordered from E9.5 to E13.5). The lines correspond to the principal graph learned by Monocle 3.
Extended Data Fig. 11 UMAP visualization of the 56 subtrajectories, coloured by inferred pseudotime.
To orient each subtrajectory (same projections as Extended Data Fig. 10), we identified one or several starting points as focal concentrations of E9.5 cells, and then computed developmental pseudotime for cells present along various paths. The lines correspond to the principal graph learned by Monocle 3.
Extended Data Fig. 12 Gene dynamics in the myogenic trajectory.
a, Genes that are differentially expressed between the Myf5 path and the Myod path highlighted in Fig. 6. Cells along each path were compared using Monocle’s differentialGeneTest function. Pseudotimes along each path were scaled from 0 to 100 independently. The full model formula was ‘~path ∗ sm.ns(Pseudotime, df=3)’, whereas the reduced model was ‘~sm.ns(Pseudotime, df=3)’. Differentially expressed genes (FDR <1%, one-sided likelihood ratio test with multiple comparisons adjusted) were clustered via Ward’s method and visualized as a heat map via the pheatmap package. b, Pseudotemporal kinetics for selected genes involved in Robo–Slit signalling. Red indicates cells on the Myod1 path, while blue corresponds to the Myf5 path. Standardized expression scores for each gene on the original myogenic trajectory are shown next to the expression curves for each. Only cells with detectable expression are rendered, to prevent overplotting. c, Modules of genes differentially expressed over the myogenic trajectory. A total of 2,908 genes were clustered via hierarchical clustering. The dendrogram was cut into 14 modules using the cutree function in R, and the aggregate expression of genes in each module was computed. Colours indicate aggregate UMI counts for each module that have been scaled for library size, log-transformed and then mapped to Z-scores to enable comparison between modules. Cells with no expression of a given module are excluded to prevent overplotting.
This file contains Supplementary Note 1, Supplementary References and full legends for Supplementary Tables 1-11
This file contains Supplementary Tables 1-11
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Cao, J., Spielmann, M., Qiu, X. et al. The single-cell transcriptional landscape of mammalian organogenesis. Nature 566, 496–502 (2019). https://doi.org/10.1038/s41586-019-0969-x
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