Transcript-guided targeted cell enrichment for scalable single-nucleus RNA sequencing

Large-scale single-cell atlases have revealed many aging- and disease-associated cell types, yet these populations are often underrepresented in heterogeneous tissues, limiting detailed molecular analyses. To address this, we developed EnrichSci-a scalable, microfluidics-free platform that combines hybridization chain reaction RNA fluorescence in situ hybridization (FISH) with combinatorial indexing to profile single-nucleus transcriptomes of target cell types with full gene-body coverage. Applied to oligodendrocytes in the aging mouse brain, EnrichSci uncovered aging-associated molecular dynamics across distinct oligodendrocyte subtypes, revealing both shared and subtype-specific gene expression changes. Additionally, we identified aging-associated exon-level signatures missed by conventional gene-level analyses, highlighting post-transcriptional regulation as a critical dimension of cell-state dynamics in aging. By coupling transcript-guided enrichment with a scalable sequencing workflow, EnrichSci provides a versatile approach to decode dynamic regulatory landscapes in diverse cell types from complex tissues.

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Publication Details

Journal
Cell Genomics
Published
2025-12-11
DOI
https://doi.org/10.1016/j.xgen.2025.101101
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

Transcript-guided targeted cell enrichment for scalable single-nucleus RNA sequencing

Jasper Lee, Zihan Xu, Manolis Maragkakis, Junyue Cao et al.
Cell Genomics
Single-cell and spatial transcriptomics
article

Transcript-guided targeted cell enrichment for scalable single-nucleus RNA sequencing

Jasper Lee, Zihan Xu, Manolis Maragkakis, Junyue Cao, Andras Sziraki, Abdulraouf Abdulraouf, Andrew Liao, Ziyu Lu, Abid Rehman, Zehao Zhang, Weirong Jiang, Wei Zhou, Alia Arya
article en

Abstract

Large-scale single-cell atlases have revealed many aging- and disease-associated cell types, yet these populations are often underrepresented in heterogeneous tissues, limiting detailed molecular analyses. To address this, we developed EnrichSci-a scalable, microfluidics-free platform that combines hybridization chain reaction RNA fluorescence in situ hybridization (FISH) with combinatorial indexing to profile single-nucleus transcriptomes of target cell types with full gene-body coverage. Applied to oligodendrocytes in the aging mouse brain, EnrichSci uncovered aging-associated molecular dynamics across distinct oligodendrocyte subtypes, revealing both shared and subtype-specific gene expression changes. Additionally, we identified aging-associated exon-level signatures missed by conventional gene-level analyses, highlighting post-transcriptional regulation as a critical dimension of cell-state dynamics in aging. By coupling transcript-guided enrichment with a scalable sequencing workflow, EnrichSci provides a versatile approach to decode dynamic regulatory landscapes in diverse cell types from complex tissues.

Cell GenomicsVol. 6(3)
National Institutes of Health (US), Institute on Aging (US), National Institute on Aging (US), Rockefeller University (US)
Openalex Percentile: Top 64%
Single-cell and spatial transcriptomics
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Transcript-guided targeted cell enrichment for scalable single-nucleus RNA sequencing — Jasper Lee, Zihan Xu, et al. · Cell Genomics (2025) | TGRS Research Map | TGRS