An ultra high-throughput method for single-cell joint analysis of open chromatin and transcriptome.


Journal

Nature structural & molecular biology
ISSN: 1545-9985
Titre abrégé: Nat Struct Mol Biol
Pays: United States
ID NLM: 101186374

Informations de publication

Date de publication:
11 2019
Historique:
received: 11 06 2019
accepted: 30 09 2019
pubmed: 7 11 2019
medline: 20 2 2020
entrez: 8 11 2019
Statut: ppublish

Résumé

Simultaneous profiling of transcriptome and chromatin accessibility within single cells is a powerful approach to dissect gene regulatory programs in complex tissues. However, current tools are limited by modest throughput. We now describe an ultra high-throughput method, Paired-seq, for parallel analysis of transcriptome and accessible chromatin in millions of single cells. We demonstrate the utility of Paired-seq for analyzing the dynamic and cell-type-specific gene regulatory programs in complex tissues by applying it to mouse adult cerebral cortex and fetal forebrain. The joint profiles of a large number of single cells allowed us to deconvolute the transcriptome and open chromatin landscapes in the major cell types within these brain tissues, infer putative target genes of candidate enhancers, and reconstruct the trajectory of cellular lineages within the developing forebrain.

Identifiants

pubmed: 31695190
doi: 10.1038/s41594-019-0323-x
pii: 10.1038/s41594-019-0323-x
pmc: PMC7231560
mid: NIHMS1561987
doi:

Substances chimiques

Chromatin 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1063-1070

Subventions

Organisme : NIMH NIH HHS
ID : U19 MH114831
Pays : United States
Organisme : NHGRI NIH HHS
ID : U54 HG006997
Pays : United States

Références

de Laat, W. & Duboule, D. Topology of mammalian developmental enhancers and their regulatory landscapes. Nature 502, 499–506 (2013).
pubmed: 24153303 doi: 10.1038/nature12753
Johnson, D. S., Mortazavi, A., Myers, R. M. & Wold, B. Genome-wide mapping of in vivo protein-DNA interactions. Science 316, 1497–1502 (2007).
pubmed: 17540862 doi: 10.1126/science.1141319
Crawford, G. E. et al. Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS). Genome Res. 16, 123–131 (2006).
pubmed: 16344561 pmcid: 1356136 doi: 10.1101/gr.4074106
Buenrostro, J. D., Giresi, P. G., Zaba, L. C., Chang, H. Y. & Greenleaf, W. J. Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position. Nat. Methods 10, 1213–1218 (2013).
pubmed: 24097267 pmcid: 3959825 doi: 10.1038/nmeth.2688
Yue, F. et al. A comparative encyclopedia of DNA elements in the mouse genome. Nature 515, 355–364 (2014).
pubmed: 25409824 pmcid: 4266106 doi: 10.1038/nature13992
The ENCODE Project Consortium. An integrated encyclopedia of DNA elements in the human genome. Nature 489, 57–74 (2012).
Kelsey, G., Stegle, O. & Reik, W. Single-cell epigenomics: Recording the past and predicting the future. Science 358, 69–75 (2017).
pubmed: 28983045 doi: 10.1126/science.aan6826
Buenrostro, J. D. et al. Single-cell chromatin accessibility reveals principles of regulatory variation. Nature 523, 486–490 (2015).
pubmed: 26083756 pmcid: 4685948 doi: 10.1038/nature14590
Cusanovich, D. A. et al. Multiplex single cell profiling of chromatin accessibility by combinatorial cellular indexing. Science 348, 910–914 (2015).
pubmed: 25953818 pmcid: 4836442 doi: 10.1126/science.aab1601
Jin, W. et al. Genome-wide detection of DNase I hypersensitive sites in single cells and FFPE tissue samples. Nature 528, 142–146 (2015).
pubmed: 26605532 pmcid: 4697938 doi: 10.1038/nature15740
Rotem, A. et al. Single-cell ChIP-seq reveals cell subpopulations defined by chromatin state. Nat. Biotechnol. 33, 1165–1172 (2015).
pubmed: 26458175 pmcid: 4636926 doi: 10.1038/nbt.3383
Harada, A. et al. A chromatin integration labelling method enables epigenomic profiling with lower input. Nat. Cell Biol. 21, 287–296 (2019).
pubmed: 30532068 doi: 10.1038/s41556-018-0248-3
Hainer, S. J., Boskovic, A., McCannell, K. N., Rando, O. J. & Fazzio, T. G. Profiling of pluripotency factors in single cells and early embryos. Cell 177, 1319–1329.e1311 (2019).
pubmed: 30955888 pmcid: 6525046 doi: 10.1016/j.cell.2019.03.014
Kaya-Okur, H. S. et al. CUT&Tag for efficient epigenomic profiling of small samples and single cells. Nat. Commun. 10, 1930 (2019).
pubmed: 31036827 pmcid: 6488672 doi: 10.1038/s41467-019-09982-5
Nagano, T. et al. Single-cell Hi-C reveals cell-to-cell variability in chromosome structure. Nature 502, 59–64 (2013).
pubmed: 24067610 doi: 10.1038/nature12593
Guo, H. et al. Single-cell methylome landscapes of mouse embryonic stem cells and early embryos analyzed using reduced representation bisulfite sequencing. Genome Res. 23, 2126–2135 (2013).
pubmed: 24179143 pmcid: 3847781 doi: 10.1101/gr.161679.113
Smallwood, S. A. et al. Single-cell genome-wide bisulfite sequencing for assessing epigenetic heterogeneity. Nat. Methods 11, 817–820 (2014).
pubmed: 25042786 pmcid: 4117646 doi: 10.1038/nmeth.3035
Mooijman, D., Dey, S. S., Boisset, J. C., Crosetto, N. & van Oudenaarden, A. Single-cell 5hmC sequencing reveals chromosome-wide cell-to-cell variability and enables lineage reconstruction. Nat. Biotechnol. 34, 852–856 (2016).
pubmed: 27347753 doi: 10.1038/nbt.3598
Zhu, C. et al. Single-cell 5-formylcytosine landscapes of mammalian early embryos and ESCs at single-base resolution. Cell Stem Cell 20, 720–731.e725 (2017).
pubmed: 28343982 doi: 10.1016/j.stem.2017.02.013
Wu, X., Inoue, A., Suzuki, T. & Zhang, Y. Simultaneous mapping of active DNA demethylation and sister chromatid exchange in single cells. Genes Dev. 31, 511–523 (2017).
pubmed: 28360182 pmcid: 5393065 doi: 10.1101/gad.294843.116
Macosko, E. Z. et al. Highly parallel genome-wide expression profiling of individual cells using nanoliter droplets. Cell 161, 1202–1214 (2015).
pubmed: 26000488 pmcid: 4481139 doi: 10.1016/j.cell.2015.05.002
Klein, A. M. et al. Droplet barcoding for single-cell transcriptomics applied to embryonic stem cells. Cell 161, 1187–1201 (2015).
pubmed: 26000487 pmcid: 4441768 doi: 10.1016/j.cell.2015.04.044
Preissl, S. et al. Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation. Nat. Neurosci. 21, 432–439 (2018).
pubmed: 29434377 pmcid: 5862073 doi: 10.1038/s41593-018-0079-3
Lake, B. B. et al. Integrative single-cell analysis of transcriptional and epigenetic states in the human adult brain. Nat. Biotechnol. 36, 70–80 (2018).
pubmed: 29227469 doi: 10.1038/nbt.4038
Luo, C. et al. Single-cell methylomes identify neuronal subtypes and regulatory elements in mammalian cortex. Science 357, 600–604 (2017).
pubmed: 28798132 pmcid: 5570439 doi: 10.1126/science.aan3351
Grosselin, K. et al. High-throughput single-cell ChIP-seq identifies heterogeneity of chromatin states in breast cancer. Nat. Genet. 51, 1060–1066 (2019).
pubmed: 31152164 doi: 10.1038/s41588-019-0424-9
Dey, S. S., Kester, L., Spanjaard, B., Bienko, M. & van Oudenaarden, A. Integrated genome and transcriptome sequencing of the same cell. Nat. Biotechnol. 33, 285–289 (2015).
pubmed: 25599178 pmcid: 4374170 doi: 10.1038/nbt.3129
Macaulay, I. C. et al. G&T-seq: parallel sequencing of single-cell genomes and transcriptomes. Nat. Methods 12, 519–522 (2015).
pubmed: 25915121 doi: 10.1038/nmeth.3370
Angermueller, C. et al. Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity. Nat. Methods 13, 229–232 (2016).
pubmed: 26752769 pmcid: 4770512 doi: 10.1038/nmeth.3728
Hou, Y. et al. Single-cell triple omics sequencing reveals genetic, epigenetic, and transcriptomic heterogeneity in hepatocellular carcinomas. Cell Res. 26, 304–319 (2016).
pubmed: 26902283 pmcid: 4783472 doi: 10.1038/cr.2016.23
Hu, Y. et al. Simultaneous profiling of transcriptome and DNA methylome from a single cell. Genome Biol. 17, 88 (2016).
pubmed: 27150361 pmcid: 4858893 doi: 10.1186/s13059-016-0950-z
Guo, F. et al. Single-cell multi-omics sequencing of mouse early embryos and embryonic stem cells. Cell Res. 27, 967–988 (2017).
pubmed: 28621329 pmcid: 5539349 doi: 10.1038/cr.2017.82
Pott, S. Simultaneous measurement of chromatin accessibility, DNA methylation, and nucleosome phasing in single cells. eLife 6, e23203 (2017).
pubmed: 28653622 pmcid: 5487215 doi: 10.7554/eLife.23203
Clark, S. J. et al. scNMT-seq enables joint profiling of chromatin accessibility DNA methylation and transcription in single cells. Nat. Commun. 9, 781 (2018).
pubmed: 29472610 pmcid: 5823944 doi: 10.1038/s41467-018-03149-4
Liu, L. et al. Deconvolution of single-cell multi-omics layers reveals regulatory heterogeneity. Nat. Commun. 10, 470 (2019).
pubmed: 30692544 pmcid: 6349937 doi: 10.1038/s41467-018-08205-7
Li, G. et al. Joint profiling of DNA methylation and chromatin architecture in single cells. Nat. Methods 16, 991–993 (2019).
pubmed: 31384045 pmcid: 6765429 doi: 10.1038/s41592-019-0502-z
Lee, D. S. et al. Simultaneous profiling of 3D genome structure and DNA methylation in single human cells. Nat. Methods 16, 999–1006 (2019).
pubmed: 31501549 pmcid: 6765423 doi: 10.1038/s41592-019-0547-z
Stoeckius, M. et al. Simultaneous epitope and transcriptome measurement in single cells. Nat. Methods 14, 865–868 (2017).
pubmed: 28759029 pmcid: 5669064 doi: 10.1038/nmeth.4380
Peterson, V. M. et al. Multiplexed quantification of proteins and transcripts in single cells. Nat. Biotechnol. 35, 936–939 (2017).
pubmed: 28854175 doi: 10.1038/nbt.3973
Cao, J. et al. Joint profiling of chromatin accessibility and gene expression in thousands of single cells. Science 361, 1380–1385 (2018).
pubmed: 30166440 pmcid: 6571013 doi: 10.1126/science.aau0730
Chen, S., Lake, B.B. & Zhang, K. High-throughput sequencing of the transcriptome and chromatin accessibility in the same cell. Nat. Biotechnol. https://doi.org/10.1038/s41587-019-0290-0 (2019).
Rosenberg, A. B. et al. Single-cell profiling of the developing mouse brain and spinal cord with split-pool barcoding. Science 360, 176–182 (2018).
pubmed: 29545511 pmcid: 7643870 doi: 10.1126/science.aam8999
Peng, X. et al. TELP, a sensitive and versatile library construction method for next-generation sequencing. Nucleic Acids Res. 43, e35 (2015).
pubmed: 25223787 doi: 10.1093/nar/gku818
Lareau, C. A. et al. Droplet-based combinatorial indexing for massive-scale single-cell chromatin accessibility. Nat. Biotechnol. 37, 916–924 (2019).
pubmed: 31235917 doi: 10.1038/s41587-019-0147-6
Cao, J. et al. Comprehensive single-cell transcriptional profiling of a multicellular organism. Science 357, 661–667 (2017).
pubmed: 28818938 pmcid: 5894354 doi: 10.1126/science.aam8940
Fang, R. et al. Fast and accurate clustering of single cell epigenomes reveals cis-regulatory elements in rare cell types. Preprint at bioRxiv https://doi.org/10.1101/615179 (2019).
Tasic, B. et al. Adult mouse cortical cell taxonomy revealed by single cell transcriptomics. Nat. Neurosci. 19, 335–346 (2016).
pubmed: 26727548 pmcid: 4985242 doi: 10.1038/nn.4216
McCarthy, D. J., Chen, Y. & Smyth, G. K. Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation. Nucleic Acids Res. 40, 4288–4297 (2012).
pubmed: 22287627 pmcid: 3378882 doi: 10.1093/nar/gks042
Khan, A. et al. JASPAR 2018: update of the open-access database of transcription factor binding profiles and its web framework. Nucleic Acids Res. 46, D260–D266 (2018).
pubmed: 29140473 doi: 10.1093/nar/gkx1126
Lai, T. et al. SOX5 controls the sequential generation of distinct corticofugal neuron subtypes. Neuron 57, 232–247 (2008).
pubmed: 18215621 doi: 10.1016/j.neuron.2007.12.023
Sun, W. et al. SOX9 is an astrocyte-specific nuclear marker in the adult brain outside the neurogenic regions. J. Neurosci. 37, 4493–4507 (2017).
pubmed: 28336567 pmcid: 5413187 doi: 10.1523/JNEUROSCI.3199-16.2017
Gorkin, D. U. et al. An atlas of dynamic chromatin landscapes in the developing mouse fetus. Nature (in the press).
Yu, M. & Ren, B. The three-dimensional organization of mammalian genomes. Annu. Rev. Cell Dev. Biol. 33, 265–289 (2017).
pubmed: 28783961 pmcid: 5837811 doi: 10.1146/annurev-cellbio-100616-060531
Fang, R. et al. Mapping of long-range chromatin interactions by proximity ligation-assisted ChIP-seq. Cell Res. 26, 1345–1348 (2016).
pubmed: 27886167 pmcid: 5143423 doi: 10.1038/cr.2016.137
Haghverdi, L., Buttner, M., Wolf, F. A., Buettner, F. & Theis, F. J. Diffusion pseudotime robustly reconstructs lineage branching. Nat. Methods 13, 845–848 (2016).
pubmed: 27571553 doi: 10.1038/nmeth.3971
Schep, A. N., Wu, B., Buenrostro, J. D. & Greenleaf, W. J. chromVAR: inferring transcription-factor-associated accessibility from single-cell epigenomic data. Nat. Methods 14, 975–978 (2017).
pubmed: 28825706 pmcid: 5623146 doi: 10.1038/nmeth.4401
Martynoga, B., Drechsel, D. & Guillemot, F. Molecular control of neurogenesis: a view from the mammalian cerebral cortex. Cold Spring Harb. Perspect. Biol. 4, a008359 (2012).
pubmed: 23028117 pmcid: 3475166 doi: 10.1101/cshperspect.a008359
Mulqueen, R. M. et al. Improved single-cell ATAC-seq reveals chromatin dynamics of in vitro corticogenesis. Preprint at bioRxiv https://doi.org/10.1101/637256 (2019).
Pliner, H. A. et al. Cicero predicts cis-regulatory DNA interactions from single-cell chromatin accessibility data. Mol. Cell 71, 858–871.e858 (2018).
pubmed: 30078726 pmcid: 6582963 doi: 10.1016/j.molcel.2018.06.044
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359 (2012).
pubmed: 22388286 pmcid: 3322381 doi: 10.1038/nmeth.1923
Dobin, A. & Gingeras, T. R. Mapping RNA-seq reads with STAR. Curr. Protoc. Bioinformatics 51, 11.14.1–11.14.19 (2015).
Zhang, Y. et al. Model-based analysis of ChIP-Seq (MACS). Genome Biol. 9, R137 (2008).
pubmed: 18798982 pmcid: 2592715
Butler, A., Hoffman, P., Smibert, P., Papalexi, E. & Satija, R. Integrating single-cell transcriptomic data across different conditions, technologies, and species. Nat. Biotechnol. 36, 411–420 (2018).
pubmed: 29608179 pmcid: 6700744 doi: 10.1038/nbt.4096
Ramirez, F., Dundar, F., Diehl, S., Gruning, B. A. & Manke, T. deepTools: a flexible platform for exploring deep-sequencing data. Nucleic Acids Res. 42, W187–W191 (2014).
pubmed: 24799436 pmcid: 4086134 doi: 10.1093/nar/gku365
Heinz, S. et al. Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. Mol. Cell 38, 576–589 (2010).
pubmed: 20513432 pmcid: 2898526 doi: 10.1016/j.molcel.2010.05.004
Subelj, L. & Bajec, M. Unfolding communities in large complex networks: combining defensive and offensive label propagation for core extraction. Phys. Rev. E Stat. Nonlin. Soft Matter Phys. 83, 036103 (2011).
pubmed: 21517554 doi: 10.1103/PhysRevE.83.036103
Angerer, P. et al. destiny: diffusion maps for large-scale single-cell data in R. Bioinformatics 32, 1241–1243 (2016).
pubmed: 26668002 doi: 10.1093/bioinformatics/btv715
Juric, I. et al. MAPS: Model-based analysis of long-range chromatin interactions from PLAC-seq and HiChIP experiments. PLoS Comput. Biol. 15, e1006982 (2019).
pubmed: 30986246 pmcid: 6483256 doi: 10.1371/journal.pcbi.1006982

Auteurs

Chenxu Zhu (C)

Ludwig Institute for Cancer Research, La Jolla, CA, USA.

Miao Yu (M)

Ludwig Institute for Cancer Research, La Jolla, CA, USA.

Hui Huang (H)

Ludwig Institute for Cancer Research, La Jolla, CA, USA.
Biomedical Sciences Graduate Program, University of California San Diego, La Jolla, CA, USA.

Ivan Juric (I)

Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.

Armen Abnousi (A)

Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.

Rong Hu (R)

Ludwig Institute for Cancer Research, La Jolla, CA, USA.

Jacinta Lucero (J)

Computational Neurobiology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA, USA.

M Margarita Behrens (MM)

Computational Neurobiology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA, USA.

Ming Hu (M)

Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.

Bing Ren (B)

Ludwig Institute for Cancer Research, La Jolla, CA, USA. biren@ucsd.edu.
Center for Epigenomics, Department of Cellular and Molecular Medicine, Institute of Genomic Medicine, Moores Cancer Center, University of California San Diego, School of Medicine, La Jolla, CA, USA. biren@ucsd.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH