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Cross-species single-cell RNA-seq data hold immense potential for unraveling cell type evolution and transferring knowledge between well-explored and less-studied species. However, challenges arise from interspecific genetic variation, batch effects stemming from experimental discrepancies and inherent individual biological differences. Here, we benchmarked nine data-integration methods across 20 species, encompassing 4.7 million cells, spanning eight phyla and the entire animal taxonomic hierarchy. Our evaluation reveals notable differences between the methods in removing batch effects and preserving biological variance across taxonomic distances. Methods that effectively leverage gene sequence information capture underlying biological variances, while generative model-based approaches excel in batch effect removal. SATURN demonstrates robust performance across diverse taxonomic levels, from cross-genus to cross-phylum, emphasizing its versatility. SAMap excels in integrating species beyond the cross-family level, especially for atlas-level cross-species integration, while scGen shines within or below the cross-class hierarchy. As a result, our analysis offers recommendations and guidelines for selecting suitable integration methods, enhancing cross-species single-cell RNA-seq analyses and advancing algorithm development.
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http://dx.doi.org/10.1093/nar/gkae1316 | DOI Listing |
J Exp Med
November 2025
Institute of Molecular Medicine, Feinstein Institutes for Medical Research, Manhasset, NY, USA.
Monocytes and macrophages in patients with lupus nephritis exhibit altered behavior compared with healthy kidneys. How to optimally use mouse models to develop treatments targeting these cells is poorly understood. This study compared intrarenal myeloid cells in four mouse models and 155 lupus nephritis patients using single-cell profiling, spatial transcriptomics, and functional studies.
View Article and Find Full Text PDFBMC Biol
September 2025
Department of Zoology, College of Life Science, Sichuan Agricultural University, Ya'an, Sichuan, 625014, China.
Background: Mammalian skin exhibits profound cellular and molecular restructuring across lifespan, yet an integrated single-cell mapping from embryogenesis to senescence remains limited. The Chenghua (CH) pig, with exceptional skin thickness characteristics, provides a promising model for investigating human skin development and physiology.
Results: We constructed a comprehensive single-cell RNA atlas of 443,529 cells from CH pig skin spanning 10 developmental stages (embryonic day 56 to postnatally year 7).
Sci Rep
August 2025
Department of Endocrinology and Metabolism, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Metabolic dysfunction-associated fatty liver disease (MAFLD), a global epidemic affecting 25% of adults, is driven by immune-metabolic dysregulation, yet the causal mechanisms linking immune cell-specific gene perturbations to disease progression remain unresolved. Current studies lack systematic integration of single-cell transcriptomics, causal inference, and functional validation to dissect actionable potential intervention targets. We combined peripheral blood mononuclear cells (PBMCs) single-cell RNA sequencing (scRNA-seq; GSE179886: 2 MAFLD vs.
View Article and Find Full Text PDFDev Cell
August 2025
Plant Systems Physiology, Department of Plant and Animal Biology, Radboud Institute for Biological and Environmental Sciences, Radboud University, 6500 AJ Nijmegen, the Netherlands; Joint Center for Single Cell Biology, Shandong Agricultural University and Radboud University, Tai'an, Shandong 271018
Uncovering plant cell types and regulatory genes across species has long been a challenge. Writing in Cell, Xue et al. present single-cell atlases for six vascular plants and identify conserved "cell-type foundational genes.
View Article and Find Full Text PDFDev Cell
August 2025
Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11724, USA. Electronic address:
Plant shoot stem cells generate organs essential for food, feed, and biofuels. However, plant single-cell analyses struggled to capture these rare cells or to detect stem cell regulators like CLAVATA3 and WUSCHEL. Here, we dissected stem cell-enriched shoot tissues from maize and Arabidopsis for single-cell RNA sequencing (scRNA-seq), and we optimized protocols to recover thousands of CLAVATA3- and WUSCHEL-expressing cells.
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