Lineage-Resolved Enhancer and Promoter Usage during a Time Course of Embryogenesis
- PMID: 33171098
- DOI: 10.1016/j.devcel.2020.10.009
Lineage-Resolved Enhancer and Promoter Usage during a Time Course of Embryogenesis
Abstract
Enhancers are essential drivers of cell states, yet the relationship between accessibility, regulatory activity, and in vivo lineage commitment during embryogenesis remains poorly understood. Here, we measure chromatin accessibility in isolated neural and mesodermal lineages across a time course of Drosophila embryogenesis. Promoters, including tissue-specific genes, are often constitutively open, even in contexts where the gene is not expressed. In contrast, the majority of distal elements have dynamic, tissue-specific accessibility. Enhancer priming appears rarely within a lineage, perhaps reflecting the speed of Drosophila embryogenesis. However, many tissue-specific enhancers are accessible in other lineages early on and become progressively closed as embryogenesis proceeds. We demonstrate the usefulness of this tissue- and time-resolved resource to definitively identify single-cell clusters, to uncover predictive motifs, and to identify many regulators of tissue development. For one such predicted neural regulator, l(3)neo38, we generate a loss-of-function mutant and uncover an essential role for neuromuscular junction and brain development.
Keywords: DNase-seq; chromatin accessibility; developmental enhancers; embryogenesis; priming; transcription-factor occupancy.
Copyright © 2020 Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of Interests The authors declare no competing interests.
Similar articles
-
The cis-regulatory dynamics of embryonic development at single-cell resolution.Nature. 2018 Mar 22;555(7697):538-542. doi: 10.1038/nature25981. Epub 2018 Mar 14. Nature. 2018. PMID: 29539636 Free PMC article.
-
The continuum of Drosophila embryonic development at single-cell resolution.Science. 2022 Aug 5;377(6606):eabn5800. doi: 10.1126/science.abn5800. Epub 2022 Aug 5. Science. 2022. PMID: 35926038 Free PMC article.
-
Developmental Transcriptional Enhancers: A Subtle Interplay between Accessibility and Activity: Considering Quantitative Accessibility Changes between Different Regulatory States of an Enhancer Deconvolutes the Complex Relationship between Accessibility and Activity.Bioessays. 2020 Apr;42(4):e1900188. doi: 10.1002/bies.201900188. Epub 2020 Mar 6. Bioessays. 2020. PMID: 32142172 Review.
-
Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development.Nat Genet. 2012 Jan 8;44(2):148-56. doi: 10.1038/ng.1064. Nat Genet. 2012. PMID: 22231485
-
Developmental enhancers and chromosome topology.Science. 2018 Sep 28;361(6409):1341-1345. doi: 10.1126/science.aau0320. Science. 2018. PMID: 30262496 Free PMC article. Review.
Cited by
-
Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.Am J Hum Genet. 2024 Oct 3;111(10):2265-2282. doi: 10.1016/j.ajhg.2024.08.019. Epub 2024 Sep 17. Am J Hum Genet. 2024. PMID: 39293448
-
Dissecting the regulatory logic of specification and differentiation during vertebrate embryogenesis.bioRxiv [Preprint]. 2024 Aug 27:2024.08.27.609971. doi: 10.1101/2024.08.27.609971. bioRxiv. 2024. PMID: 39253514 Free PMC article. Preprint.
-
cisDynet: An integrated platform for modeling gene-regulatory dynamics and networks.Imeta. 2023 Nov 23;2(4):e152. doi: 10.1002/imt2.152. eCollection 2023 Nov. Imeta. 2023. PMID: 38868212 Free PMC article.
-
Enhancer-promoter interactions become more instructive in the transition from cell-fate specification to tissue differentiation.Nat Genet. 2024 Apr;56(4):686-696. doi: 10.1038/s41588-024-01678-x. Epub 2024 Mar 11. Nat Genet. 2024. PMID: 38467791 Free PMC article.
-
Chromatin accessibility profiling methods.Nat Rev Methods Primers. 2021;1:10. doi: 10.1038/s43586-020-00008-9. Epub 2021 Jan 21. Nat Rev Methods Primers. 2021. PMID: 38410680 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Molecular Biology Databases