Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.09.25.754561

A single-nucleus multi-omic atlas of gene regulation across 21 adult human tissues

Abstract

Diverse human cell types establish specialized functions through lineage- and context-specific regulatory programs. Interpreting non-coding genetic risk requires integrated multi-omic reference maps that directly connect regulatory DNA to cellular expression across human tissues. Here we present a single-nucleus multi-omic atlas comprising 459,856 transcriptomic and chromatin accessibility profiles from 21 adult human tissues and four donors, including paired measurements from 160,688 nuclei. The atlas resolves nine cell lineages, 61 broad cell types and 313 subclusters, and identifies 1,085,062 candidate cis-regulatory elements (cCREs), including 161,270 novel elements absent from ENCODE. Regulatory activity was dominated by cell identity but refined by tissue context. Joint profiling enabled 871,177 cCRE-gene associations and revealed lineage-specific regulatory architectures. Cross-tissue accessibility further identified lineage-restricted and constitutively inaccessible chromatin domains, the latter showing preferential hypomethylation across human cancers. Furthermore, we leverage this dataset to train sequence-to-function models to predict chromatin-accessibility effects for 548,656 fine-mapped variants, identifying 18,133 high-effect variants, including 1,120 broadly active variants. Models trained for eight endothelial subtypes further resolve predicted variant effects across vascular beds. Together, this atlas provides a comprehensive cellular and computational framework for interpreting regulatory sequence, context-dependent gene control, and complex trait genetics across the human body.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Fan, K., Sule, A., Guillaumet-Adkins, A., Zhang, R., Yu, T., Cao, Z., Zhang, X., Durand, N., Tellier, M., Domenech, L., Aguet, F., Buenrostro, J. D., Ardlie, K. G.. 2026-09-27. A single-nucleus multi-omic atlas of gene regulation across 21 adult human tissues. https://doi.org/10.64898/2026.09.25.754561

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Longitudinal miRNA-mRNA Profiling Reveals Network Reorganization in Preeclampsia

Background: Preeclampsia (PE) is a leading cause of maternal and perinatal morbidity. Temporal dynamics of molecular dysregulation across pregnancy remain poorly understood. We performed longitudinal RNA sequencing of maternal whole blood to characterize miRNA-mRNA regulatory network evolution in PE. Methods: Whole-blood samples from early (M1: 10-18 weeks) and late pregnancy (M2: 32-38 weeks) were analyzed from 43 PE cases and 106 normotensive controls, including 109 paired samples (36 PE cases, 73 controls). Differential expression, temporal classification, pathway enrichment, and miRNA-mRNA network integration were performed. Placental expression support was assessed using internal RNA-seq and public databases. Key miRNA-mRNA interactions were experimentally validated in HTR-8/SVneo trophoblast cells. Results: PE exhibited marked temporal reorganization of miRNA-mRNA networks, with strongly opposing temporal effect sizes across overlapping miRNA and mRNA features (Spearman {rho} = -0.82, P < 0.0001). PI3K/AKT/mTORC1 signaling showed biphasic reversal (NES = +1.46, FDR = 0.028 at M1; NES = -1.64, FDR = 0.025 at M2), and heme-metabolism programs showed progressive suppression (2.1-fold NES intensification; FDR < 0.05 at both timepoints). Network analysis identified 29 high-confidence biphasic miRNA-mRNA pairs, including convergent targeting of ADGRA2 by three miRNAs and HSD17B1 by three miRNAs. miR-101-3p overexpression reduced DEPP1 mRNA (~40%) and protein (~26%) in trophoblast cells (P < 0.01), supporting a FOXO-DEPP1 axis. Blood-derived pairs showed pathway convergence with placental VGLL3-centered programs (PI3K/AKT, FOXO, TGF-{beta}, trophoblast differentiation). Conclusions: PE is associated with predominantly stage-specific or biphasic miRNA-mRNA network reorganization, with PI3K/AKT/mTORC1 dynamic remodeling and progressive heme-metabolism suppression. These findings support gestational-age-specific biomarker development and identify regulatory axes, including miR-101-3p [->] DEPP1, for mechanistic investigation.

genomics↗

MicroDUET: a dual-headed genomic foundation model for pathogen surveillance

Pathogen genomic surveillance works from raw reads, assembled genomes and alignments, representations that are slow and costly to compare at scale. Compact embeddings from genomic language models offer an alternative, but surveillance requires resolving both evolutionary ancestry (phylogeny) and phenotypic capability (function) - which need not co-vary. Here we present MicroDUET, which adapts a 26.6-million-parameter ProkBERT backbone with two 3.5-million-parameter adapter heads: a phylogeny head trained contrastively on genome windows from the same microbes, and a function head trained to identify genes across taxa. On held-out retrieval benchmarks, the phylogeny head returned the correct species for 80.3% and 66.6% of cellular and viral queries, and the function head the correct gene family for 97.3% and 97.2%, reaching 74.4% accuracy on an independent antimicrobial resistance-class benchmark. Across all three benchmarks MicroDUET outranked 17 other genomic encoders. Without training on lineage, clade or drug-susceptibility tasks, MicroDUET identified Mycobacterium tuberculosis and mpox virus lineages and clades (0.965, 0.975 accuracy), discriminated rifampicin resistance without lineage adjustment (AUROC 0.985), and retrospectively identified an emerging mpox lineage as anomalous (AUROC 0.974). MicroDUET operates 10^3 - 10^4 times faster than single-threaded sequence-based alignments. MicroDUET therefore provides a compact, reusable representation for scalable pathogen surveillance and sequence triage.

genomics↗

A chromosome-level genome assembly of northern dragonhead, Dracocephalum ruyschiana L., 1753

We present a chromosome-level genome assembly for the vascular plant northern dragonhead, Dracocephalum ruyschiana. The assembly comprises two pseudo-haplotypes, hap1 and hap2, of 661 Mb and 681 Mb, with 93.6% and 92.5%, respectively, scaffolded into seven chromosomes each - in line with the known karyotype. Assembly quality was high, with conserved single-copy ortholog completeness scores of 97.9% and 97.8%, combined k-mer completeness of 98.1%, and 38,141 and 38,617 annotated protein-coding genes for hap1 and hap2, respectively. This assembly provides a high-quality genomic resource for future research and conservation of northern dragonhead, as well as the endangered northern dragonhead sap beetle, which depends on the plant for reproduction and whose genome assembly is described in a complementary genome note.

genomics↗