A human cell atlas of fetal gene expression
Open accessAbstract
The genomics of human development: Understanding the trajectory of a developing human requires an understanding of how genes are regulated and expressed. Two papers now present a pooled approach using three levels of combinatorial indexing to examine the single-cell gene expression and chromatin landscapes from 15 organs in fetal samples. Cao et al. focus on measurements of RNA in broadly distributed cell types and provide insights into organ specificity. Domcke et al. examined the chromatin accessibility of cells from these organs and identify the regulatory elements that regulate gene expression. Together, these analyses generate comprehensive atlases of early human development. Science , this issue p. eaba7721 , p. eaba7612
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In silico deletion of TBX5 in fetal cardiomyocytes more significantly impacted its direct targets (as defined by ChIP-seq) compared to indirect targets and housekeeping genes.
“Analogously, in silico deletion of TBX5, another known congenital heart disease gene, in fetal cardiomyocytes23 more significantly impacted its direct targets (as defined by ChIP-seq34) compared to indirect targets and housekeeping genes (Extended Data Fig. 9f).”
From Transfer learning enables predictions in network biology (2023) · cites this paper as [23]
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- Authors
- Cao, J., O’Day, D. R., Pliner, H. A., Kingsley, P. D., Deng, M., Daza, R. M., Zager, M. A., Aldinger, K. A., Blecher-Gonen, R., Zhang, F., Spielmann, M., Palis, J., Doherty, D., Steemers, F. J., Glass, I. A., Trapnell, C., & Shendure, J.
- Affiliations
- University of Washington (US)
- Brotman Baty Institute (US)
- University of Rochester Medicine (US)
- Fred Hutch Cancer Center (US)
- Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
- Illumina (United States) (US)
- Max Planck Institute for Molecular Genetics (DE)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Trapnell, Cole
- Shendure, Jay
- ORCID
- Venue
- Science
- Published
- 2020-11-13
- Volume
- 370
- Issue
- 6518
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC7780123
- OpenAlex
- W3103797259
- Cited by
- 764
- References
- 23
- Citations by year
- 2026: 104 · 2025: 134 · 2024: 147 · 2023: 118 · 2022: 148 · 2021: 102 · 2020: 8 · 2019: 1 · 2013: 1
- FWCI
- 30.82
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- Funders
- National Institutes of Health (NICHD R24HD000836)
- Howard Hughes Medical Institute
- NIH Office of the Director (R01 DK119285)
- Deutsche Forschungsgemeinschaft (SP1532/3-1, SP1532/4-1, SP1532/5-1)
- Paul G. Allen Frontiers Foundation (Allen Discovery Center grant)
- Brotman Baty Institute for Precision Medicine
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- human fetal development, cell specification, single-cell gene expression, chromatin accessibility, fetal tissue, cell type annotation, fetal erythropoiesis, adrenal gland, endothelial cells, epithelial cells
- MeSH terms
- Atlases as Topic, Chromatin, Fetus, Humans, Neurons, Transcription Factors, Gene Expression Regulation, Developmental, Gene Expression Profiling, Single-Cell Analysis
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